SCI, SSCI VE AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

MYH9-related Disease Caused by an R1165C Mutation in a Child With Previous Diagnosis of Immune Thrombocytopenic Purpura
Keskin E. Y. , Yuceer R. O. , Baspinar S., OKUR E., BERDELİ A.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, cilt.43, sa.8, 2021 (SCI İndekslerine Giren Dergi) identifier
 
PRIMARY HYPEROXALURIA TYPE 1 PROGRESSING TO END-STAGE RENAL FAILURE AT INFANCY
KAÇAR A., ADAR M., Sancaktar M., KAYA AKSOY G., ÇOMAK E., KOYUN M., et al.
PEDIATRIC NEPHROLOGY, cilt.36, sa.10, ss.3463, 2021 (SCI İndekslerine Giren Dergi) identifier
 
A rare cause of urolithiasis in an infant: Questions
KOYUN M., Sancaktar M., KAYA AKSOY G., ÇOMAK E., KAÇAR A., ADAR M., et al.
PEDIATRIC NEPHROLOGY, cilt.36, ss.2065-0, 2021 (SCI İndekslerine Giren Dergi) identifier identifier identifier
 
Four diseases, PLAID, APLAID, FCAS3 and CVID and one gene (PHOSPHOLIPASE C, GAMMA-2; PLCG2): Striking clinical phenotypic overlap and difference
Kütükçüler N. , Berdeli A. , Güven Bilgin R. B. , Aykut A., Durmaz A. , Çoğulu M. Ö. , et al.
Clinical Case Studies, cilt.9, sa.4, ss.2023-2031, 2021 (SCI Expanded İndekslerine Giren Dergi)  Creative Commons License
 
Four diseases, PLAID, APLAID, FCAS3 and CVID and one gene (PHOSPHOLIPASE C, GAMMA- 2; PLCG2): Striking clinical phenotypic overlap and difference. 2021;00:1–9
Kütükçüler N. , Yılmaz E. , Berdeli A. , Aykut A. , Durmaz A. , Çoğulu M. Ö. , et al.
Clinical Case Studies, cilt.00, ss.1-9, 2021 (SCI Expanded İndekslerine Giren Dergi) 
 
Demographic and clinical characteristics of children with autosomal dominant polycystic kidney disease: a single center experience
DEMİR B. K. , Mutlubas F., Soyaltin E., Alparslan C., Arya M., Alaygut D., et al.
TURKISH JOURNAL OF MEDICAL SCIENCES, cilt.51, sa.2, ss.772-777, 2021 (SCI İndekslerine Giren Dergi)   identifier identifier identifier 
 
A rare cause of urolithiasis in an infant: Answers
KOYUN M., Sancaktar M., KAYA AKSOY G., ÇOMAK E., KAÇAR A., ADAR M., et al.
PEDIATRIC NEPHROLOGY, 2021 (SCI İndekslerine Giren Dergi) identifier identifier identifier
 
Inflammasomes and their regulation in periodontal disease: A review.
Aral K., Milward M., Kapila Y., Berdeli A. , Cooper P.
Journal of periodontal research, cilt.55, ss.473-487, 2020 (SCI İndekslerine Giren Dergi) identifier identifier identifier 
 
Differential expression of inflammasome regulatory transcripts in periodontal disease.
Aral K., Berdeli E., Cooper P., Milward M., Kapila Y., Karadede Ü., et al.
Journal of periodontology, cilt.91, ss.606-616, 2020 (SCI İndekslerine Giren Dergi) identifier identifier identifier 
 
NLRP3 GENE MUTATION IN A PATIENT WITH RECURRENT APHTHOUS LESIONS
Kinar A., Bucak A., Ulu S., BERDELİ A.
ACTA MEDICA MEDITERRANEA, cilt.36, sa.2, ss.1083-1087, 2020 (SCI İndekslerine Giren Dergi)  identifier identifier
 
TBC1D8B Mutations Implicate RAB11-Dependent Vesicular Trafficking in the Pathogenesis of Nephrotic Syndrome.
Kampf L., Schneider R., Gerstner L., Thünauer R., Chen M., Helmstädter M., et al.
Journal of the American Society of Nephrology : JASN, cilt.30, ss.2338-2353, 2019 (SCI İndekslerine Giren Dergi) identifier identifier identifier 
 
Genetics and Consequences of Atypical Hemolytic-uremic Syndrome in Turkish Children
CONKAR S. , Mir S., BERDELİ A.
IRANIAN JOURNAL OF KIDNEY DISEASES, cilt.13, sa.5, ss.317-322, 2019 (SCI İndekslerine Giren Dergi)  identifier identifier identifier
 
Genetics and outcome of atypical hemolytic-uremic syndrome in Turkish children: a retrospective study between 2010 and 2017, a single-center experience.
Conkar S., Mir S., Berdeli A.
Iranian journal of kidney diseases, cilt.13, ss.316-321, 2019 (SCI Expanded İndekslerine Giren Dergi) identifier identifier
 
Distribution of nucleotide variants in the DNA sequence of ERCC1 and XRCC1 genes and the effect of phenotype in patients with gastric cancer.
Asgerov E., Şenol Ö., Güler A., Berdeli A.
The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology, cilt.30, ss.517-523, 2019 (SCI İndekslerine Giren Dergi)  Creative Commons License  identifier identifier identifier 
 
NPHS2 gene sequencing results in children of the Azerbaijani population with different types of nephrotic syndrome caused by chronic glomerulonephritis.
Baylarov R., Baylarova R., Berdeli A. , Bayramov R., Haziyev E.
Bratislavske lekarske listy, cilt.120, ss.102-105, 2019 (SCI İndekslerine Giren Dergi)  Creative Commons License identifier identifier identifier 
 
HEREDITARY HYPOMAGNESAEMIA WITH SECONDARY HYPOCALCEMIA: REPORT OF TWO SIBLINGS WITH LONG-TERM FOLLOW-UP
Gozmen S. K. , Serdaroglu E., Basaran C., BERDELİ A.
PEDIATRIC NEPHROLOGY, cilt.33, sa.10, ss.1913, 2018 (SCI İndekslerine Giren Dergi) identifier
 
NPHS2 GENE MUTATIONS IN AZERBAIJAN CHILDREN WITH STEROID-RESISTANT NEPHROTIC SYNDROME
Baylarov R., Senol O., Atan M., BERDELİ A.
PEDIATRIC NEPHROLOGY, cilt.33, sa.10, ss.1933, 2018 (SCI İndekslerine Giren Dergi) identifier
 
Infant onset severe complement-mediated hemolytic uremic syndrome complicated by secondary sclerosing cholangitis
Yesilbas O., Sevketoglu E., Petmezci M. T. , Kihtir H. S. , Benzer M., Arikan C., et al.
JOURNAL OF CLINICAL APHERESIS, cilt.33, sa.5, ss.619-623, 2018 (SCI İndekslerine Giren Dergi) identifier identifier identifier 
 
Fever-induced Brugada syndrome in a 9-year-old boy presenting with acute chest pain.
Besli G., Yıldırım S., Akalın İ., Ayhan Y., Kısıoğlu M., Berdeli A.
The Turkish journal of pediatrics, cilt.60, ss.571-575, 2018 (SCI İndekslerine Giren Dergi)  Creative Commons License identifier identifier identifier 
 
A novel mutation of interleukin-1 receptor antagonist (IL1RN) in a DIRA patient from Turkey: Diagnosis and treatment.
Sözeri B., Gerçeker-Türk B., Yıldız-Atıkan B., Mir S., Berdeli A.
The Turkish journal of pediatrics, cilt.60, ss.588-592, 2018 (SCI İndekslerine Giren Dergi)  Creative Commons License identifier identifier identifier 
 
THE ROLE OF NEU1 GENE IN THE ETIOPATHOGENESIS OF HENOCH SCHONLEIN VASCULITIS AND ITS RELATIONSHIP WITH RENAL INVOLVEMENT
BahCeci N. B. , Ertan P., Yuksel S., Nese N., Horasan G. D. , BERDELİ A.
PEDIATRIC NEPHROLOGY, cilt.32, sa.9, ss.1730, 2017 (SCI İndekslerine Giren Dergi) identifier
 
DISTAL RENAL TUBULAR ACIDOSIS WITH TRANSIENT PROFOUND HYPERCALCEMIA IN TWO SIBLINGS
Basaran C., Gozmen S. K. , Devrim F., Ozdemir K., BERDELİ A. , Serdaroglu E.
PEDIATRIC NEPHROLOGY, cilt.32, sa.9, ss.1815, 2017 (SCI İndekslerine Giren Dergi) identifier
 
POSSIBLE ROLE OF COMPLEMENT CASCADE IN HSPN/IGAN; A CASE REPORT
Pinarbasi A. S. , DURSUN İ., Gunduz Z., Poyrazoglu H., AKGÜN H., BERDELİ A. , et al.
PEDIATRIC NEPHROLOGY, cilt.32, sa.9, ss.1748, 2017 (SCI İndekslerine Giren Dergi) identifier
 
CLINICAL SIGNIFICANCE OF GENETIC VARIANTS IN PATIENTS WITH C3 GLOMERULOPATHIES
Oruc A., Yildiz A., Vuruskan B., BERDELİ A. , Yavuz M., Dilek K., et al.
NEPHROLOGY DIALYSIS TRANSPLANTATION, cilt.32, 2017 (SCI İndekslerine Giren Dergi) identifier
 
FAS/FASL gene polymorphisms in Turkish patients with chronic myeloproliferative disorders.
OZDEMIRKIRAN F. G. , Nalbantoglu S., Gokgoz Z., PAYZIN B. K. , Vural F. , ÇAĞIRGAN S., et al.
Archives of medical science : AMS, cilt.13, sa.2, ss.426-432, 2017 (SCI İndekslerine Giren Dergi)   Creative Commons License identifier identifier identifier 
 
Efficacy and safety of eculizumab in adult patients with atypical hemolytic uremic syndrome: A single center experience from Turkey
Gediz F., Payzin B. K. , Ecemis S., Guler N., Yilmaz A. F. , Topcugil F., et al.
TRANSFUSION AND APHERESIS SCIENCE, cilt.55, sa.3, ss.357-362, 2016 (SCI İndekslerine Giren Dergi)  identifier identifier identifier 
 
TRCP-6 Mutation Causing FSGS in Childhood
Aksoy G. K. , KOYUN M., ÇOMAK E., BERDELİ A. , Gemici A., AKKAYA B., et al.
PEDIATRIC NEPHROLOGY, cilt.31, sa.10, ss.1834, 2016 (SCI İndekslerine Giren Dergi) identifier
 
Role of Toll-Like Receptors in Tuberculosis Infection
Biyikli O. O. , Baysak A., Ece G., Oz A. T. , ÖZHAN M. H. , BERDELİ A.
JUNDISHAPUR JOURNAL OF MICROBIOLOGY, cilt.9, sa.10, 2016 (SCI İndekslerine Giren Dergi)   Creative Commons License  identifier identifier identifier 
 
Can Urinary Nerve Growth Factor and Brain-Derived Neurotrophic Factor be used in the Diagnosis and Follow-Up of Voiding Dysfunction in Children?
Özdemir K., Dinçel N., Berdeli A. , Mir S.
Urology journal, cilt.13, ss.2690-6, 2016 (SCI İndekslerine Giren Dergi) identifier identifier identifier
 
Prevalence and significance of MEFV gene mutations in patients with sarcoidosis
KOBAK S., SEVER F., GÖKSEL Ö. , GÖKSEL T. , Orman M. N. , BERDELİ A.
SCANDINAVIAN JOURNAL OF RHEUMATOLOGY, cilt.45, sa.3, ss.215-218, 2016 (SCI İndekslerine Giren Dergi)   identifier identifier identifier 
 
NOD2/CARD15 gene mutations in patients with gouty arthritis
KARAARSLAN A., KOBAK Ş., BERDELİ A.
BOSNIAN JOURNAL OF BASIC MEDICAL SCIENCES, cilt.16, sa.4, ss.276-279, 2016 (SCI İndekslerine Giren Dergi)   Creative Commons License identifier identifier identifier 
 
Fc gamma receptor polymorphisms in patients with transient hypogammaglobulinemia of infancy presenting with mild and severe infections
KÜTÜKÇÜLER N. , AZARSIZ E. , KARACA N. , AKSU G. , BERDELİ A.
ASIAN PACIFIC JOURNAL OF ALLERGY AND IMMUNOLOGY, cilt.33, sa.4, ss.312-319, 2015 (SCI İndekslerine Giren Dergi)   Creative Commons License identifier identifier identifier 
 
Development of a medication adherence scale for familial Mediterranean fever (MASIF) in a cohort of Turkish children.
Yesilkaya S., Acikel C., Fidanci B., Polat A., Sozeri B., Ayaz N., et al.
Clinical and experimental rheumatology, cilt.33, 2015 (SCI İndekslerine Giren Dergi) identifier identifier identifier
 
Thrombotic Microangiopathy with Complement Factor H Gene Mutations Unassociated with Atypical Hemolytic Uremic Syndrome
Oymak Y., Karapinar T. H. , Ay Y., Ozcan E., Muminoglu N., Koker S. A. , et al.
TURKISH JOURNAL OF HEMATOLOGY, cilt.32, sa.3, ss.275-276, 2015 (SCI İndekslerine Giren Dergi)  Creative Commons License identifier identifier identifier 
 
Myostatin Gene Polymorphism in an Elderly Sarcopenic Turkish Population
TOSUN TAŞAR P., ŞAHİN S. , KARAMAN E. , OZ A., ULUSOY M. G. , DUMAN S. , et al.
GENETIC TESTING AND MOLECULAR BIOMARKERS, cilt.19, sa.8, ss.457-460, 2015 (SCI İndekslerine Giren Dergi)   identifier identifier identifier 
 
Prevalence and risk factors of sarcopenia in elderly nursing home residents
Tasar P. T. , ŞAHİN S. , KARAMAN E. , ULUSOY M. S. , DUMAN S. , BERDELİ A. , et al.
EUROPEAN GERIATRIC MEDICINE, cilt.6, sa.3, ss.214-219, 2015 (SCI İndekslerine Giren Dergi)  identifier identifier 
 
PREVALENCE AND SIGNIFICANCE OF MEFV GENE MUTATIONS IN PATIENTS WITH SARCOIDOSIS
Kobak S., Sever F., GÖKSEL Ö. , GÖKSEL T. , ORMAN M. N. , BERDELİ A.
ANNALS OF THE RHEUMATIC DISEASES, cilt.74, ss.405-406, 2015 (SCI İndekslerine Giren Dergi) identifier
 
Prevalance and risk factors of sarcopenia in elderly nursing home resident
TOSUN TAŞAR P., ŞAHİN S. , KARAMAN E. , BERDELİ A. , DUMAN S. , AKÇİÇEK S. F.
Eupean Geriatric Medicine, 2015 (SCI Expanded İndekslerine Giren Dergi)
 
A newborn with pertussis accompanying nephrotic syndrome.
Kaynak-Türkmen M., Cengiz-Erdem F., Sönmez F., Girişgen İ., Telli M., Berdeli A.
The Turkish journal of pediatrics, cilt.56, ss.665-8, 2014 (SCI İndekslerine Giren Dergi) identifier identifier identifier
 
Can Urinary Ngf And Bdnf Be Used In The Diagnosis And Treatment Follow-up Of Bladder Dysfunction In Children?
Ozdemir K., Mir S., Dincel N. , BERDELİ A.
PEDIATRIC NEPHROLOGY, cilt.29, sa.9, ss.1804, 2014 (SCI İndekslerine Giren Dergi) identifier
 
The predictive value of urinary UPIb mRNA levels in VUR and recurrent urinary tract infections.
Bulut İ. , Mir S., Berdeli A. , Sozeri B.
Clinical nephrology, cilt.81, ss.152-8, 2014 (SCI İndekslerine Giren Dergi) identifier identifier identifier 
 
Escherichia coli brain abscess in a twin pair associated with TLR4 gene mutation
Erdemir A., Kahramaner Z., Cosar H., Turkoglu E., Sutcuoglu S., Uygun D. K. , et al.
PEDIATRICS INTERNATIONAL, cilt.55, sa.4, ss.516-518, 2013 (SCI İndekslerine Giren Dergi)  identifier identifier identifier 
 
NPHS2 Gene Mutation Results in Turkish SRNS Children and Genotype-phenotype Correlations
Berdeli A. , Mir S., Dincel N.
PEDIATRIC NEPHROLOGY, cilt.28, sa.8, ss.1451, 2013 (SCI İndekslerine Giren Dergi) identifier
 
CARD15/NOD2 MUTATIONS IN TURKISH PATIENTS WITH ANKYLOSING SPONDYLITIS
Kobak S., ORMAN M. N. , BERDELİ A.
ANNALS OF THE RHEUMATIC DISEASES, cilt.72, ss.821-822, 2013 (SCI İndekslerine Giren Dergi) identifier
 
A novel DAX-1 mutation presented with precocious puberty and hypogonadotropic hypogonadism in different members of a large pedigree
Durmaz E., Turkkahraman D., BERDELİ A. , Atan M., KARAGÜZEL G., Akcurin S., et al.
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, cilt.26, ss.551-555, 2013 (SCI İndekslerine Giren Dergi)  identifier identifier identifier 
 
Lack of association between macrophage migration inhibitory factor gene promoter (-173 G/C) polymorphism and childhood Henoch-Schonlein purpura in Turkish patients
Nalbantoglu S., TABEL Y., Mir S., BERDELİ A.
CYTOKINE, cilt.62, sa.1, ss.160-164, 2013 (SCI İndekslerine Giren Dergi)  identifier identifier identifier 
 
SPP1 Gene Polymorphisms Associated With Nephrolithiasis in Turkish Pediatric Patients
Tekin G., Ertan P., Horasan G., BERDELİ A.
UROLOGY JOURNAL, cilt.9, sa.4, ss.640-647, 2012 (SCI İndekslerine Giren Dergi)  identifier identifier identifier
 
The polymorphisms of genes that affect the endothelium in primary hypertension of childhood
Sozeri B. , Ozdemir Y. , BERDELİ A. , Mir S.
PEDIATRIC NEPHROLOGY, cilt.27, sa.9, ss.1734, 2012 (SCI İndekslerine Giren Dergi) identifier
 
Ouantitative mRNA Expression of Podoctye Proteins in Children With Steroid Resistant Nephrotic Syndrome
Dincel N., Berdeli A. , Mir S.
PEDIATRIC NEPHROLOGY, cilt.27, sa.9, ss.1721, 2012 (SCI İndekslerine Giren Dergi) identifier
 
Variability in the age at diagnosis of diabetes in two unrelated patients with a homozygous glucokinase gene mutation
Durmaz E., Flanagan S., BERDELİ A. , Semiz S., Akcurin S., Ellard S., et al.
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, cilt.25, ss.805-808, 2012 (SCI İndekslerine Giren Dergi)   identifier identifier identifier 
 
Interleukin 8 gene 2767 A/G polymorphism is associated with increased risk of nephritis in children with Henoch-Schonlein purpura
TABEL Y., Mir S., BERDELİ A.
RHEUMATOLOGY INTERNATIONAL, cilt.32, sa.4, ss.941-947, 2012 (SCI İndekslerine Giren Dergi)   identifier identifier identifier 
 
Renal Scarring and Osteopontin Gene C/T Polymorphism in Children With Primary Vesicoureteral Reflux
Erdogan H., Mir S., BERDELİ A. , Aksu N.
INDIAN PEDIATRICS, cilt.49, sa.4, ss.311-313, 2012 (SCI İndekslerine Giren Dergi)  identifier identifier identifier 
 
Gene Polymorphism of Complement Factor H in a Turkish Patient With Membranoproliferative Glomerulonephritis Type II
Sozeri B., Mir S., Berdeli A. , Dincel N., Sarsik B.
IRANIAN JOURNAL OF KIDNEY DISEASES, cilt.6, sa.2, ss.149-153, 2012 (SCI İndekslerine Giren Dergi)  identifier identifier identifier
 
A Molecular Case Report of Autosomal Dominant Retinitis Pigmentosa: RP1/RHO Sequence Variants in a Turkish Family
Nalbantoglu S. M. , Shahbazov C., BERDELİ A.
OMICS-A JOURNAL OF INTEGRATIVE BIOLOGY, cilt.16, ss.18-23, 2012 (SCI İndekslerine Giren Dergi)   identifier identifier identifier 
 
LY96, UPKIB Mutations and TLR4, CD14, MBL Polymorphisms in Children with Urinary Tract Infection
Ertan P., BERDELİ A. , Yilmaz O., Gonulal D. A. , Yuksel H.
INDIAN JOURNAL OF PEDIATRICS, cilt.78, sa.10, ss.1229-1233, 2011 (SCI İndekslerine Giren Dergi)  identifier identifier identifier 
 
SPP1 gene polymorphisms associated with nephrolithiasis in Turkish pediatric patients
Tekin G., Ertan P., Horasan G. D. , BERDELİ A.
PEDIATRIC NEPHROLOGY, cilt.26, sa.9, ss.1638, 2011 (SCI İndekslerine Giren Dergi) identifier
 
The effectiveness or the effectiveless of CYP3A4 polymorphism on calsineurin inhibitor drugs trough levels in pediatric kidney transplantations
Toroslu E., Sozeri B. , Mir S., BERDELİ A.
PEDIATRIC NEPHROLOGY, cilt.26, sa.9, ss.1601-1602, 2011 (SCI İndekslerine Giren Dergi) identifier
 
The effect of mutations NR3C2 in children with primary hypertension
KARA Ö. , Sozeri B. , Mir S., BERDELİ A. , Dincel N.
PEDIATRIC NEPHROLOGY, cilt.26, sa.9, ss.1727, 2011 (SCI İndekslerine Giren Dergi) identifier
 
Might there be an association between lamin A/C mutation and polycystic kidney disease in patients with dilated cardiomyopathy?
Sozeri B. , Mir S., BERDELİ A. , Dincel N.
PEDIATRIC NEPHROLOGY, cilt.26, sa.9, ss.1710-1711, 2011 (SCI İndekslerine Giren Dergi) identifier
 
Association of Angiotensin-Converting Enzyme I/D and eNOS G894T Gene Polymorphisms with Erectile Dysfunction
Cam F. S. , Gumus B. H. , Var A., BERDELİ A.
TURKIYE KLINIKLERI TIP BILIMLERI DERGISI, cilt.31, sa.2, ss.432-437, 2011 (SCI İndekslerine Giren Dergi)   Creative Commons License identifier identifier 
 
Effect of Colchicine-Resistant Familial Mediterranean Fever on Growth Parameters
Sozeri B. , Yilmaz E. , Mir S., BERDELİ A.
TURKISH JOURNAL OF RHEUMATOLOGY, cilt.26, sa.1, ss.1-6, 2011 (SCI İndekslerine Giren Dergi)   Creative Commons License identifier identifier 
 
Association of FAS-670A/G and FASL-843C/T Gene Polymorphisms on Allograft Nephropathy in Pediatric Renal Transplant Patients
Ertan P., Mir S., Ozkayin N., BERDELİ A.
IRANIAN JOURNAL OF PEDIATRICS, cilt.20, sa.4, ss.442-450, 2010 (SCI İndekslerine Giren Dergi)  identifier identifier identifier
 
Clinical and genetic aspects of Turkish hepatocellular carcinoma patients: Results of a single center study
Kazimi M. C. , Nalbantoglu S., Kilic M., BERDELİ A.
INTERNATIONAL JOURNAL OF THE PHYSICAL SCIENCES, cilt.5, sa.15, ss.2379-2392, 2010 (SCI İndekslerine Giren Dergi)   identifier identifier
 
Familial Mediterranean Fever and Pras Scoring System
YILMAZ E., Sozeri B. , BERDELİ A. , Mir S.
PEDIATRIC NEPHROLOGY, cilt.25, sa.9, ss.1930, 2010 (SCI İndekslerine Giren Dergi) identifier
 
The Effectiveness or the Effectiveless of CYP3A4 Polymorphism on Calsineurin Inhibitor Drugs Trough Levels in Pediatric Kidney Transplantations
Toroslu E., Sozeri B. , Mir S., BERDELİ A.
PEDIATRIC NEPHROLOGY, cilt.25, sa.9, ss.1946, 2010 (SCI İndekslerine Giren Dergi) identifier
 
Outcome of Focal Segmental Glomerulosclerosis after Renal Transplantation with/without Podocine Gene Mutations in Turkish Children
Mutlubas F., Sozeri B. , BERDELİ A. , Hoscoskun C., Mir S.
PEDIATRIC NEPHROLOGY, cilt.25, sa.9, ss.1894, 2010 (SCI İndekslerine Giren Dergi) identifier
 
Immunosuppressive Treatment Responses in Steroid Resistant Nephrotic Syndrome with Podocine Gene Mutation Positive and Negative Turkish Children
Mir S., Mutlubas F., BERDELİ A. , KARA Ö.
PEDIATRIC NEPHROLOGY, cilt.25, sa.9, ss.1877, 2010 (SCI İndekslerine Giren Dergi) identifier
 
MEFV Gene Single Nucleotid Polymorphisms and Their Clinical Relevance
YILMAZ E., Sozeri B. , Mir S., BERDELİ A.
PEDIATRIC NEPHROLOGY, cilt.25, sa.9, ss.1930-1931, 2010 (SCI İndekslerine Giren Dergi) identifier
 
Specific Podocin Mutations with Clinical Features in Steroid-Resistant Nephrotic Syndrome in Turkish Children
Mutlubas F., Mir S., BERDELİ A. , Dincel N.
PEDIATRIC NEPHROLOGY, cilt.25, sa.9, ss.1878, 2010 (SCI İndekslerine Giren Dergi) identifier
 
Interleukin 8 Gene 2767 A/G Polymorphism Is Associated with Increased Risk of Nephritis in Children with Henoch Schonlein Purpura
TABEL Y., Mir S., BERDELİ A.
PEDIATRIC NEPHROLOGY, cilt.25, sa.9, ss.1920, 2010 (SCI İndekslerine Giren Dergi) identifier
 
CLINICAL QUIZ A UMOD storage disease
Mir S., Yavascan O., Mutlubas F., BERDELİ A. , ŞEN S.
PEDIATRIC NEPHROLOGY, cilt.25, sa.1, ss.83-86, 2010 (SCI İndekslerine Giren Dergi) identifier identifier 
 
MEFV gene full DNA sequence analysis in familial Mediterranean fever (FMF) and healthy controls
Dirican A., KİTAPÇIOĞLU G. , BERDELİ A. , KABASAKAL Y.
CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, cilt.27, sa.5, ss.715, 2009 (SCI İndekslerine Giren Dergi) identifier
 
GENETIC AND NON-GENETIC TYPE OF STEROID-RESISTANT NEPHROTIC SYNDROME AND CYCLOSPORINE A RESPONSE
Ozsan F. M. , Mir S., BERDELİ A.
PEDIATRIC NEPHROLOGY, cilt.24, sa.9, ss.1806-1807, 2009 (SCI İndekslerine Giren Dergi) identifier
 
Are Monocyte Chemoattractant Protein-1-2518 G and Regulated Activation Normal T Cell Expressed and Secreted-403 A Alleles Risk Factor for Periodontitis?
Oezcaka O., Bicakci N., Kroese T., BERDELİ A.
TURKISH JOURNAL OF BIOCHEMISTRY-TURK BIYOKIMYA DERGISI, cilt.34, sa.3, ss.139-147, 2009 (SCI İndekslerine Giren Dergi)  identifier identifier
 
Podocin mutations in a patient with congenital nephrotic syndrome and cardiac malformation
Sonmez F., Mir S., BERDELİ A. , Aydogdu S. A. , Altincik A.
PEDIATRICS INTERNATIONAL, cilt.50, sa.6, ss.828-830, 2008 (SCI İndekslerine Giren Dergi) identifier identifier identifier 
 
G protein beta 3 subunit gene polymorphism in Turkish hypertensives
Alioglu E., Ercan E., Tengiz I., Yildiz A., Tuerk U. O. , Saygi S., et al.
ANADOLU KARDIYOLOJI DERGISI-THE ANATOLIAN JOURNAL OF CARDIOLOGY, cilt.8, sa.5, ss.331-335, 2008 (SCI İndekslerine Giren Dergi)  identifier identifier identifier
 
Aortic stiffnes may be a marker in management of renal replascement therapy in children with chronic kidney disease?
Sozeri B. Y. , KARA Ö. , Levent E., Mir S., Yavascan O., BERDELİ A.
PEDIATRIC NEPHROLOGY, cilt.23, sa.9, ss.1613, 2008 (SCI İndekslerine Giren Dergi) identifier
 
The influence of alpha-adducin gene polymorphism on response of blood pressure to exercise in patients with hypertension
Alioglu E., ERCAN E., Tengiz I., Turk U., ERGÜN M. , Akgoz S., et al.
EUROPEAN HEART JOURNAL, cilt.29, ss.224, 2008 (SCI İndekslerine Giren Dergi) identifier
 
Mutation in the UMOD gene responsible for familial juvenile hyperuricemic nephropathy and chronic renal failure: Case report
Mir S., BERDELİ A. , Yavascan O., Mutlubas F.
PEDIATRIC NEPHROLOGY, cilt.23, sa.9, ss.1693, 2008 (SCI İndekslerine Giren Dergi) identifier
 
TRPC6 gene mutations in children with sporadic and familial steroid resistant nephritic syndrome (SRNS) originating from Turkey
Mir S., BERDELİ A. , Yavascan O.
PEDIATRIC NEPHROLOGY, cilt.23, sa.9, ss.1592, 2008 (SCI İndekslerine Giren Dergi) identifier
 
New genetic non-HLA risk markers in chronic allograft nephropaty
YILMAZ E., Mir S., BERDELİ A.
PEDIATRIC NEPHROLOGY, cilt.23, sa.9, ss.1689, 2008 (SCI İndekslerine Giren Dergi) identifier
 
Familial vesicoureteral reflux with PAX2/EYA1 gene mutation in a Turkish family
Mir S., BERDELİ A. , Mutlubas F.
ACTA PAEDIATRICA, cilt.97, ss.257-258, 2008 (SCI İndekslerine Giren Dergi) identifier
 
A case of hypomagnesemia with secondary hypocalcemia caused by Trpm6 gene mutation
Apa H., Kayserili E., Agin H., Hizarcioglu M., Gulez P., BERDELİ A.
INDIAN JOURNAL OF PEDIATRICS, cilt.75, sa.6, ss.632-634, 2008 (SCI İndekslerine Giren Dergi)  identifier identifier identifier 
 
FC gamma receptor polymorphism: a risk factor for urinary tract infections?
Mir S., YILMAZ E., BERDELİ A. , Ozdemir R.
ACTA PAEDIATRICA, cilt.97, ss.63, 2008 (SCI İndekslerine Giren Dergi) identifier
 
LACK OF ASSOCIATION BETWEEN MCP-1 GENE POLYMORPHISM (-2518G/A) AND PREMATURE CORONARY ARTERY DISEASE
Cam F. S. , Sekuri C., Sagcan A., Ercan E., Tengiz I., Alioglu E., et al.
ATHEROSCLEROSIS SUPPLEMENTS, cilt.9, sa.1, ss.107, 2008 (SCI İndekslerine Giren Dergi) identifier 
 
Can toll-like receptor 2 polymorphism affect the phenotype of heterozygous?
BERDELİ A. , Aktay A. N. , ÖZEN S., Demirkaya E., ÖZALTIN F., TOPALOĞLU R., et al.
CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, cilt.26, sa.2, ss.188, 2008 (SCI İndekslerine Giren Dergi) identifier
 
Association of endothelial nitric oxide synthase (ENOS) gene polymorphism with chronic allograft nephropathy in turkish renal transplant recipients
Yilmaz E., Mir S., Berdeli A.
PEDIATRIC NEPHROLOGY, cilt.22, sa.9, ss.1585, 2007 (SCI İndekslerine Giren Dergi) identifier
 
Are polymorphisms of MCP-1, IL 6 and fas genes a risk factors for acute renal allograft rejection in children?
Yilmaz E., Berdeli A. , Mir S., Yavascan O., Mutlubas F., Kabasakal C.
PEDIATRIC NEPHROLOGY, cilt.22, sa.9, ss.1478, 2007 (SCI İndekslerine Giren Dergi) identifier
 
No association of interleukin-6 gene polymorphism (-174 G/C) with premature coronary artery disease in a Turkish cohort
Sekuri C., Cam F. S. , Sagcan A., Ercan E., Tengiz I., Alioglu E., et al.
CORONARY ARTERY DISEASE, cilt.18, sa.5, ss.333-337, 2007 (SCI İndekslerine Giren Dergi)  identifier identifier identifier 
 
Association of macrophage migration inhibitory factor gene-173 G/C polymorphism with prognosis in turkish children with juvenile rheumatoid arthritis
BERDELI G. , Oezyuerek A. R. , Uelger Z. , Guerses D., Levent E., Salar K., et al.
RHEUMATOLOGY INTERNATIONAL, cilt.26, sa.8, ss.726-731, 2006 (SCI İndekslerine Giren Dergi)  identifier identifier identifier 
 
Association of macrophage migration inhibitory factor-173C allele polymorphism with steroid resistance in children with nephrotic syndrome
Berdeli A. , Mir S., Ozkayin N., Serdaroglu E., Tabel Y., Cura A.
PEDIATRIC NEPHROLOGY, cilt.20, sa.11, ss.1566-1571, 2005 (SCI İndekslerine Giren Dergi)  identifier identifier identifier 
 
Adjunctive subantimicrobial dose doxycycline: effect on clinical parameters and gingival crevicular fluid transforming growth factor-beta(1) levels in severe, generalized chronic periodontitis
Gurkan A. , CINARCIK S. , HUSEYINOV A.
JOURNAL OF CLINICAL PERIODONTOLOGY, cilt.32, sa.3, ss.244-253, 2005 (SCI İndekslerine Giren Dergi)  identifier identifier identifier 
 
Gingival crevicular fluid monocyte chemoattractant protein-1 and RANTES levels in patients with generalized aggressive periodontitis
EMINGIL G. , Atilla G. , HUSEYINOV A.
JOURNAL OF CLINICAL PERIODONTOLOGY, cilt.31, sa.10, ss.829-834, 2004 (SCI İndekslerine Giren Dergi)  identifier identifier identifier 
 
Plasma and liver carnitine status of children with chronic liver disease and cirrhosis
Selimoğlu M. A. , Aydogdu S. , Yagci R., Huseyinov A. , HUSEYİNOV A.
PEDIATRICS INTERNATIONAL, cilt.43, sa.4, ss.391-395, 2001 (SCI İndekslerine Giren Dergi)  identifier identifier 
 
Proinflammatory cytokines, prostaglandins and zinc in febrile convulsions
Tutuncuoglu S., Kutukculer N., Kepe L., Coker C., Berdeli A. , Tekgul H.
PEDIATRICS INTERNATIONAL, cilt.43, sa.3, ss.235-239, 2001 (SCI İndekslerine Giren Dergi)  identifier identifier identifier 

Diğer Hakemli Dergilerde Yayınlanan Makaleler

 
Typical Rett syndrome in a young boy with hemizygous c.316CT mutation in MECP2 gene
Coşkun M., Erbilgin S., Akalın İ., Kaya İ., Gülle Z. N. , Berdeli A.

Dusunen Adam-Journal of Psychiatry and Neurological Sciences, cilt.33, sa.1, ss.99-103, 2020 (ESCI İndekslerine Giren Dergi) identifier identifier 

 
NPHS2 Gene Mutations in Azerbaijani Children with Steroid-Resistant Nephrotic Syndrome
Baylarov R., Senol O., Atan M., Berdeli A.

SAUDI JOURNAL OF KIDNEY DISEASES AND TRANSPLANTATION, cilt.31, ss.144-149, 2020 (ESCI İndekslerine Giren Dergi)  identifier identifier identifier 

  
Treatment of familial mediterranean fever with canakinumab in patients who are unresponsive to colchicine.
Berdeli A. , Şenol Ö., Talay G.

European journal of rheumatology, cilt.6, ss.85-88, 2019 (ESCI İndekslerine Giren Dergi)   Creative Commons License identifier identifier 

 
A Rare Case of Cholestasis: Arthrogryposis, Renal Tubular Disorder and Cholestasis Syndrome
Turkmenoglu Y., Acar Y., Ozdemir F. C. , Singer R., BERDELİ A. , Adal S. E.

JOURNAL OF PEDIATRIC RESEARCH, cilt.5, sa.3, ss.161-163, 2018 (ESCI İndekslerine Giren Dergi)   Creative Commons License identifier 

 
Retrospective Investigation of Interleukin 1 and 6 Gene Polymorphism among Elderly Patients with Sarcopenia in the Turkish Population
TOSUN TAŞAR P., KARAMAN E. , KARAŞAHİN Ö., ÖZ A., ŞAHİN S. , DUMAN S. , et al.

Genetics Molecular Research, cilt.17, sa.1, 2018 (Diğer Kurumların Hakemli Dergileri)  identifier 

 
Recombinase Activating Gene 1 Deficiencies Without Omenn Syndrome May Also Present With Eosinophilia and Bone Marrow Fibrosis.
Ulusoy E., Karaca N. , Azarsiz E. , Berdeli A. , Aksu G. , Kutukculer N.

Journal of clinical medicine research, cilt.8, ss.379-84, 2016 (Diğer Kurumların Hakemli Dergileri)  Creative Commons License identifier 

 
Novel VPS33B mutations of G514S gene cause an arthrogryposis, renal dysfunction and cholestasis syndrome
CONKAR S. , MİR S., BERDELİ A.

International Journal of Case Reports and Images, cilt.7, ss.216, 2016 (Diğer Kurumların Hakemli Dergileri)  Creative Commons License  

 
Glikojen Depo Tip 1 Hastalarında İntersellüler Adezyon Molekülü Tip 1 Gen Polimorfizmin Ateroskleroza Etkisi
KALKAN UÇAR S. , BERDELİ A. , ÇOKER M.
THE JOURNAL OF PEDIATRIC RESEARCH, cilt.2, ss.7-10, 2015 (Diğer Kurumların Hakemli Dergileri)
 
Astım ve Alerjik Rinitli Çocuklarda Toll Like Reseptör 2 ve Toll Like Reseptör 4 Polimorfizmi
GÜLEN F. , Köksoy H., TANAÇ R., BERDELİ A. , DEMİR E. , ZEYREK C. D. , et al.
JOURNAL OF PEDIATRIC RESEARCH, cilt.1, sa.1, ss.13-21, 2014 (Diğer Kurumların Hakemli Dergileri) 

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

Yeni Nesil Dizileme Kullanılarak 3230 Bireyde Tespit Edilen MEFV Varyantlarının Allel Frekansları ve Genotip Dağılımlarının Analizi
Kırnaz B., Gezgin Y. , Berdeli A.
10. Ulusal Moleküler Biyoloji ve Biyoteknoloji Kongresi, Sivas, Türkiye, 18 Aralık 2021, cilt.1, ss.31 
 
OTULIN Gen Varyantlarının Yeni Nesil Dizileme Kullanılarak Değerlendirilmesi ve Bu Varyantların in silico Analizleri
Gezgin Y. , Kırnaz B., Berdeli A.
10. Ulusal Moleküler Biyoloji ve Biyoteknoloji Kongresi, Sivas, Türkiye, 18 Aralık 2021, cilt.1, ss.30
 
Glomerüler Elektron Mikroskopi Bulgularının Atipik Hemolitik Üremik Sendrom Tanısındaki Önemi
DÖLARSLAN M. E. , BARDAK S., AKÇALI E., COŞKUN YILMAZ B., BALLI E., YUYUCU KARABULUT Y., et al.
36. ULUSAL NEFROLOJİ KONGRESİ, Antalya, Türkiye, 16 – 20 Ekim 2019
 
Atipik Hemolitik Üremik Sendrom ve Pauci-immun Kresentrik Glomerulonefrit : Nadir Birliktelik
DÖLARSLAN M. E. , AKÇALI E., BARDAK S., AKPOLAT N., BERDELİ A. , TURGUTALP K., et al.
36. Ulusal Nefroloji Kongresi, Türkiye, 16 – 20 Ekim 2019
 
Kompleman İlişkili aHUS Olgu Serisi: Klinik Özellikler, Tedavi ve Gözlem Sonuçları:
DÖLARSLAN M. E. , BARDAK S., AKÇALI E., TURGUTALP K., DEMİR S., TOMBAK A., et al.
: 36. Ulusal Nefroloji Kongresi, Antalya, Türkiye, 16 – 20 Ekim 2019
 
A new KCNQ2 mutation and clinical findings
Gumus A. A. , Bilgic D. G. , BERDELİ A. , Genis E., Cam S.
52nd Conference of the European-Society-of-Human-Genetics (ESHG), Gothenburg, İsveç, 15 – 18 Haziran 2019, cilt.27, ss.1860 identifier
 
Nefrotik Düzeyde Proteinüri Ve Fokal Segmental Glomerüloskleroz Saptanan Dent Hastalığı Olgusu
TORUN BAYRAM M., YILDIZ G., BERDELİ A. , ÜNLÜ Ş. M. , SOYLU A., KAVUKÇU S.
10. Uluslarası Katılımlı Çocuk Nefroloji Kongresi, Türkiye, 1 – 04 Mayıs 2019
 
GENETICALLY INTERESTING FAMILY WITH NEPHROTICSYNDROME IN THREE SIBLINGS
ÇELAKIL M., BERDELİ A. , EKİNCİ Z., BOZKAYA YÜCEL B., BEK K.
ESPN 2018, 3 – 06 Ekim 2018
 
The effects of mesenchymal stem cell on the macrophage phenotype
BERDELİ A. , ÖZDEMİR A., ÖZDEMİR R., SARIBOYACI A.
15th International Symposium on Dendritic Cells(DC), Aachen, Almanya, 10 Haziran 2018, ss.157
 
Türk Populasyonundaki Sarkopenik Yaşlılarda IL-1,IL-6 Gen Polimorfizminin Retrospektif Olarak İncelenmesi:
TOSUN TAŞAR P., KARAMAN E. , KARAŞAHİN Ö., OZ A., ŞAHİN S. , DUMAN S. , et al.
11.Akademik Geriatri Kongresi, Antalya, Türkiye, 19 – 23 Nisan 2018, ss.92
 
Children with autosomal dominant polycystic kidney disease:Single center experience.
KASAP DEMİR B., Mutlubaş F., Soyaltın E., Alparslan C., EĞLENOĞLU ALAYGUT D., ARSLANSOYU ÇAMLAR S., et al.
4th Congress of Mediterranean Kidney Society, 20 – 22 Nisan 2018
 
Fallot Tetralojili Olgularda Genetik Varyasyon Klinik Sonuçları Nasıl Etkiliyor?
TİRYAKİ S., ÜLGER TUTAR Z. , BERDELİ A.
17. Ulusal Pediatrik Kardiyoloji ve Kalp Cerrahisi Kongresi, Türkiye, 18 – 21 Nisan 2018
 
Fallot tetralojili hastalarda Genetik varyasyon klinik sonuçları nasıl etkiliyor?
TİRYAKİ S., BERDELİ A. , ÜLGER TUTAR Z.
17.Ulusal Pediatrik Kardiyoloji ve kakp cerrahisi kongresi, Türkiye, 18 – 21 Nisan 2018
 
Kronik Menenjit ile seyreden Kronik İnfantil Nörolojik Kutanöz ve Artiküler Sendrom Olgusu
ŞAHBUDAK Z., KAHRAMAN A., AVCI G., KURUGÖL N. Z. , BERDELİ A. , ÖZKINAY F. F.
10. ULUSAL ÇOCUK ENFEKSİYON HASTALIKLARI KONGRESİ 5-9 NİSAN 2017 / MAXX ROYAL, BELEK, ANTALYA, Antalya, Türkiye, 5 – 10 Nisan 2018
 
CAPS HASTALARDA KANAKİNUMAB KULLANIMI ve KLİNİK ETKİNLİĞİ
Conkar S. , Berdeli A.
4. ulusal çocuk romatoloji kongresi, Muğla, Türkiye, 4 – 07 Nisan 2018 
 
HOW DOES GENETIC VARIATIONS AFFECT CLINICALOUTCOMES IN TETRALOGY OF FALLOT CASES?
TİRYAKİ S., BERDELİ A. , ÜLGER TUTAR Z.
Erciyes Medical Genetics Days 2018, 7 – 10 Mart 2018
 
Genetic Analysis of Phenylketonuria Patients Treated with sapropterin.
KÖSE E., BERDELİ A. , TEKE KISA P., ARSLAN N.
14th Middle East Metabolic Group Meeting, Athens, Yunanistan, 9 – 11 Şubat 2018
 
PODOSİT HÜCRE MODELİNDE PROTEİNÜRİDE, SLİT DİYAFRAM PROTEİNLERİ GENLERİNİN EKSPRESYONU VE FARMAKOLOJİK MODÜLASYONU
ANGIN M. , HÜR E., DİNÇKAL Ç., GÖKALP C., BERDELİ A. , DUMAN S.
34. Ulusal Nefroloji, Hipertansiyon, Diyaliz ve Transplantasyon Kongresi®, 18 – 21 Ekim 2017 
 
Associatation of Thrombomodulin -1748 G/C Polymorphism and Plasma Thrombomodulin with Diabetic Microvascular Complications
ERMİŞ T., ÖZGÖNÜL A. M. , SAYGILI L. F. , KARADENİZ M., BERDELİ A. , TURGAN N., et al.
TBD, 19 – 23 Eylül 2017 
 
Association of Thrombomodulin-1748 G/C polymorphism and plasma thrombomodulin with diabetic microvascular complications
Ermiş T., Turgan N., Sezer E. , Özgönül A. M. , Karadeniz M., Saygılı L. F. , et al.
Uluslararası Biyokimya Kongresi, Erzurum, Türkiye, 19 – 23 Eylül 2017 
 
The Role of NEU1 Gene İn The Etiopathogenesis of Henoch Schönlein Vasculitis and İts Relationship with Renal Involvement
BAHCECİ N. B. , ERTAN P., YÜKSEL S., NESE N., DİNÇ HORASAN G., BERDELİ A.
50th Anniversary Meeting of The Eurpean Society For Paediatric Nephrology/Glasgow, 6 – 09 Eylül 2017
 
The Effect of Growth Hormone Therapy on Plasma Phenylalanine Level in Patient with Phenylketonuria: Case Report
KÖSE E., ACAR S., DEMİR K., BERDELİ A. , ARSLAN N.
13th International Congress of Inborn Errors Of Metabolism, 5 – 09 Eylül 2017
 
Biochemical and Genetic Investigation of Phenylketonuria Patients Treated with Sapropterin
KÖSE E., BERDELİ A. , ARSLAN N.
13th International Congress of Inborn Errors Of Metabolism, 5 – 09 Eylül 2017
 
CLINICAL SIGNIFICANCE OF GENETIC IN PATIENTS WITH C3 GLOMERULOPATHIES
ORUÇ A., YILDIZ A., BERDELİ A. , YAVUZ M., DİLEK K., GÜLLÜLÜ M., et al.

ERA-EDTA 54th Congress, Madrid, İspanya, 3 – 06 Haziran 2017, cilt.32, ss.154  Creative Commons License identifier 

 
Henoch-Schönlein Vasküliti Etyopatogenezinde Nörominidaz 1 (NEU 1) Geninin Yeri ve Böbrek Tutulumu ile İlişkisi
BAHCECİ N. B. , ERTAN P., YÜKSEL S., NESE N., DİNÇ HORASAN G., BERDELİ A.
2. Uluslarası Lisansüstü Eğitim Kongresi/Manisa, 12 – 14 Mayıs 2017
 
NGS method in genetic autoinflammatory disease.
BERDELİ A.
9th International Congress of Familial Mediterranean Fever and Systemic Auto-Inflammatory Diseases, ., Kıbrıs (Kktc), 07 Mayıs 2017
 
Canakinumab treatment in Turkish Colchicine resistant patients.
BERDELİ A. , DURAN G., GURİS C.
9th International Congress of Familial Mediterranean Fever and Systemic Auto-Inflammatory Diseases, ., Kıbrıs (Kktc), 07 Mayıs 2017
 
ASSESSMENT OF SYSTEMIC VASCULAR INVOLVEMENT IN CHILDREN WITH UVEITIS
CONKAR S. , Güven Yılmaz S. , ÖZGÜR KOSKA İ., BERDELİ A. , MİR M. S.
9th International Congress of Familial Mediterranean Fever and Systemic Auto-Inflammatory Diseases., 4 – 07 Mayıs 2017, ss.33
 
Targeted NGS study in 120 patients from Turkish population with autoinflammatory symptoms without MEFV gene mutations.
BERDELİ A. , ATAN M., BAGDATLİ N., ÖZKAN D., MAHBOUB S.
9th International Congress of Familial Mediterranean Fever and Systemic Auto-Inflammatory Diseases, Girne, Kıbrıs (Kktc), 4 – 07 Mayıs 2017, ss.37
 
Treatment of Familial Mediterranean Fever with Canakinumab in Patients Unresponsive to Colchicine
BERDELİ A. , TALAY G., GURİS C., OZ A.
9th International Congress of Familial Mediterranean Fever and Systemic Auto-Inflammatory Diseases., Girne, Kıbrıs (Kktc), 4 – 07 Mayıs 2017, ss.37 identifier identifier
 
Büyüme Hormonu Tedavisinin Plazma Fenilalanini Üzerine Etkisi: Olgu Sunumu
KÖSE E., ACAR S., DEMİR K., BERDELİ A. , ARSLAN N.
14. Uluslararası Katılımlı Ulusal Metabolik Hastalıklar ve Beslenme Kongresi, 26 – 30 Nisan 2017
 
IgM Yüksekliğinin Eşlik Ettiği Primer İmmün Yetmezlik Olgularımız: Tek Merkez Deneyimi
HAZAR SAYAR E., KAPAKLI H., KELEŞ S., GÜNER Ş. N. , KARASELEK M. A. , BERDELİ A. , et al.
12. Uluslararası Katılımlı Çocuk Allerji ve Astım Kongresi, 23 Nisan 2017 – 26 Nisan 2147
 
KOLŞİSİNE DİRENÇLİ AİLEVİ AKDENİZ ATEŞİ OLGULARININ KANAKİNUMAB İLE BAŞARILI YÖNETİMİ
EREN AKARCAN S. , AKSU G. , BERDELİ A. , KARACA N. , KÜTÜKÇÜLER N.
3. KLİNİK İMMÜNOLOJİ KONGRESİ, Türkiye, 12 – 15 Nisan 2017
 
Sleep qualıty and related factors ın the elderly.
KAYABEKİR M., TOSUN TAŞAR P., TİMUR Ö., YILMAZ KİPER T., KARAŞAHİN Ö., ŞAHİN S. , et al.

International Congress on Academic Geriatrics 2017, Antalya, Türkiye, 12 – 16 Nisan 2017, ss.31-32 identifier identifier identifier 

 
Efficacy and safety of eculizumab in adult patients with atypical hemolytic uremic syndrome:a single center experience from turkey
BERDELİ A. , PAYZIN B. K. , GEDIZ F., ECEMIS S.
7th İnternational Eurosian Hematology Congress, İstanbul, Türkiye, 13 Ekim 2016, ss.48-49
 
Novel PSMB8 gene mutations in Turkish PRAAS Patients.
BERDELİ A. , ATAN M., MAHBOUB S.
PRES 2016, Genova, İtalya, 29 Eylül 2016
 
Diverse Clinical phenotypes in recombinase activating gene 1 deficiency
ULUSOY e., KARACA N. , AKSU G. , BERDELİ A. , KÜTÜKÇÜLER N.

ESID 2016, 21 – 24 Eylül 2016  Creative Commons License identifier identifier identifier 

 
PREVALENCE AND SIGNIFICANCE OF MEFV GENE MUTATIONS IN PATIENTS WITH GOUTY ARTHRITIS
Kobak S., Karaarslan A., Kaya I., Intepe N., ORMAN M. N. , BERDELİ A.
Annual European Congress of Rheumatology (EULAR), London, Kanada, 8 – 11 Haziran 2016, cilt.75, ss.115 identifier
 
NOD2/CARD15 GENE MUTATIONS IN PATIENTS WITH GOUTY ARTHRITIS
Karaarslan A., Kobak S., BERDELİ A.
Annual European Congress of Rheumatology (EULAR), London, Kanada, 8 – 11 Haziran 2016, cilt.75, ss.384 identifier
 
MEFV gene mutaions in Azerbaijan FMF patients.
BERDELİ A.
8th International Congress of Familial Mediterranean Fever and Systemic Auto-Inflammatory Diseases., Dresden, Almanya, 30 Eylül 2015
 
MEFV gene mutation distrubition in Azerbaijan FMF patients
BERDELİ A. , MİR M. S. , MUSAYEV A.
. 8th International Congress of Familial Mediterranean Fever and Systemic Auto-Inflammatory Diseases, Dresden, Almanya, 30 Eylül 2015
 
Validity and reliability of medication adherence scale in FMF
BERDELİ A.

8th International Congress of Familial Mediterranean Fever and Systemic Autoinflammatory Diseases, Almanya, 30 Eylül – 03 Ekim 2015, cilt.13, ss.70-105 identifier identifier 

 
MEFV gene mutation distrubution in Azerbaijan population
BERDELİ A.
8th International Congress of Familial Mediterranean Fever and Systemic Autoinflammatory Diseases, Almanya, 30 Eylül – 03 Ekim 2015, cilt.13, ss.75-105
 
Turkish DIRA patient with novel IL1RN gene mutation
MİR M. S. , BERDELİ A.
8th International Congress of Familial Mediterranean Fever and Systemic Autoinflammatory Diseases, Almanya, 30 Eylül – 03 Ekim 2015, cilt.13, ss.94-105
 
P109Developing of a new scale for assessing the adherence to colchicinetreatment in pediatric patients with FMF
BERDELİ A.
8th International Congress of Familial Mediterranean Fever and Systemic Autoinflammatory Diseases, Almanya, 30 Eylül – 03 Ekim 2015, cilt.13
 
ROLE OF CTLA4 POLYMORPHISM IN IDIOPATHIC NEPHROTIC SYNDROME AND TREG LEVELS
MİR M. S. , BERDELİ A.
48Th Annual Scientific Meeting Of The European society for paediatric nephrolgy(ESPN 2015), New-York, Amerika Birleşik Devletleri, 3 – 05 Eylül 2015, cilt.30, ss.1686-1687 identifier
 
MUTATION IN COMPLEMENT SYSTEM GENES OF HEMOLYTIC UREMIC SYNDROME GENOTYPE PHENOTYPE CORRELATION AND TREATMENT
MİR M. S. , SÖZERİ B., BERDELİ A.
48Th Annual Scientific Meeting Of The European society for paediatric nephrolgy(ESPN 2015), Amerika Birleşik Devletleri, 3 – 05 Eylül 2015, cilt.30, ss.1644-1645 identifier
 
SCL5A2 GENE MUTATIONS IN TURKISH CHILDREN WITH RENAL GLYCOSURIA
BERDELİ A. , SARITAŞ S.
48Th Annual Scientific Meeting Of The European society for paediatric nephrolgy(ESPN 2015), New-York, Amerika Birleşik Devletleri, 3 – 05 Eylül 2015, cilt.30, ss.1676 identifier
 
A PATIENT SEEMING AS ARPKD CLINICALLY AND AS ADPKD GENETICALLY
GEMİCİ A., KAYA AKSOY G., KOYUN M., BERDELİ A. , AKMAN S.
48Th Annual Scientific Meeting Of The European society for paediatric nephrolgy(ESPN 2015), Amerika Birleşik Devletleri, 3 – 05 Eylül 2015, cilt.30, ss.1595-1596 identifier
 
GENOTYPE PHENOTYPE CORRELATION OF TURKISH CHILDREN WITH AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY DISEASE
MİR M. S. , BERDELİ A.
48Th Annual Scientific Meeting Of The European society for paediatric nephrolgy(ESPN 2015), Amerika Birleşik Devletleri, 3 – 05 Eylül 2015, cilt.30, ss.1675 identifier
 
MOLECULAR GENETIC ANALYSES IN TURKISH CHILDREN WITH ALPORT SYNDROME
BERDELİ A. , EĞLENOĞLU ALAYGUT D.
48Th Annual Scientific Meeting Of The European society for paediatric nephrolgy(ESPN 2015), Amerika Birleşik Devletleri, 3 – 05 Eylül 2015, cilt.30, ss.1676 identifier
 
MEFV gene mutation in Turkish Sarcoiidosis patients .
BERDELİ A.
EULAR 2015, Rome, İtalya, 10 Haziran 2015
 
CARD15/NOD2 MUTATIONS IN TURKISH PATIENTS WITH ANKYLOSING SPONDYLITIS ANNALS OF THE RHEUMATIC DISEASES
BERDELİ A. , KOBAK S., ORMAN M. N.
EULAR 2015, Roma, İtalya, 10 Haziran 2015, ss.821-822
 
PREVALENCE AND SIGNIFICANCE OF MEFV GENE MUTATIONS IN PATIENTS WITH SARCOIDOSIS
BERDELİ A. , KOBAK Ş.
annual european congress of rheumatology, roma, İtalya, 10 – 13 Haziran 2015, ss.90-91
 
Matrix metalloproteinase MMP 8 and tissue inhibitor of MMP 1 TIMP 1 gene polymorphisms in generalized aggressive periodontitis gingival crevicular fluid MMP 8 and TIMP 1 levels and outcome of periodontal therapy
EMİNGİL G. , Han B., GÜRKAN A. , BERDELİ A. , Taina T., Tuula S., et al.

Europerio 8, 3 – 06 Haziran 2015 identifier identifier identifier 

 
MUTATIONS IN INFANTIL NEPHROTIC SYNDROME AND WORSE PROGNOSTIC RESULTS OF E117K POLYMORPHISM IN NPHS1
Yilmaz E., Dincel N., Bulut İ. , Hacikara S., BERDELİ A. , Mir S.

52nd Congress of the European-Renal-Association-European-Dialysis-and-Transplant-Assocation, London, Kanada, 28 – 31 Mayıs 2015, cilt.30  Creative Commons License identifier 

 
Turk populasyonundaki sarkopenik yaslilarda MSTN gen poliformizi
TOSUN TAŞAR P., ŞAHİN S. , KARAMAN E. , ATİLLA O., GULSAH MERVE U., DUMAN S. , et al.
8. Akademik Geriatri Kongresi, Türkiye, 16 – 19 Nisan 2015
 
Herediter fruktoz intoleransı iki kardeş olgu
MELİS K., EBRU C., HAVVA Y., KALKAN UÇAR S. , BERDELİ A. , ÇOKER M.
XIII. Metabolik Hastalıklar ve Beslenme Kongresi-14-18 Nisan 2015, Adana, Türkiye, 14 – 18 Nisan 2015
 
MEN-4 Sendromu
Yıldırım Şimşir I. , Ertan Y. , Sözbilen M., Makay Ö. , ERDOĞAN M. , Çetinkalp Ş. , et al.
I. Ege Endokrin Hastalıkları ve Genetik Sempozyumu, İzmir, Türkiye, 25 Şubat 2015, ss.1
 
MEN4 Sendromu
ILGIN y. ş. , ERTAN Y. , SÖZBİLEN E. M. , MAKAY Ö. , ERDOĞAN M. , ÇETİNKALP Ş. , et al.
1.Ege Endokrin Hastalıklar ve Genetik Sempozyumu, Türkiye, 25 – 27 Şubat 2015
 
FCG Receptor Polymorphisms in Patients with Transient Hypogammaglobulinemia of Infancy Presenting Mild and Severe Infections
AZARSIZ E., KÜTÜKÇÜLER N. , KARACA N., AKSU G. , BERDELİ A.
16th Biennial Meeting of the European-Society-for-Immunodeficiencies, Prague, Çek Cumhuriyeti, 29 Ekim – 01 Kasım 2014, cilt.34 identifier
 
The clinical and genetic features of patients with hyperimmunoglobulin D syndrome (HIDS)
BERDELİ A. , SÖZERİ B., ÇAM Ö., MİR M. S. , DELEBE M.
21st European Pediatric Rheumatology (PReS) Congress., Belgrade, Sırbistan Ve Karadağ, 17 Eylül 2014, ss.257
 
Diagnosis of early-onset sarcoidosis with non–classical symptoms
BERDELİ A. , SÖZERİ B., POYRAZOGLU H., DUSUNSEL R., GÜNDÜZ Z., PAÇ KISAARSLAN A.
21st European Pediatric Rheumatology (PReS) Congress, Belgrade, Sırbistan Ve Karadağ, 17 Eylül 2014, ss.269
 
The role of toll like receptors on tuberculosis infection.
BERDELİ A. , BIYIKLI O. O.
European Respiratory Society Annual Congress 2013, Barcelona, İspanya, 07 Eylül 2013, ss.4626 
 
RENAL AGENESIS AND HYOPLASIA IN HUMANS ARE NOT ASSOCIATED GLIAL CELL LINE-DERIVED NEUROTROPHIC FACTOR
BERDELİ A. , EVRENGÜL H.
PRESS, 2013, ., İngiltere, 04 Haziran 2013
 
ANGIOTENSIN 2 TYPE1/TYPE2 GENE POLYMORPHISMS IN TURKISH CHILDREN WITH VESICOURETERAL REFLUX AND RECURRENT URINARY TRACT INFECTIONS
BERDELİ A. , ERTAN P., SAHİN S., EVRENGÜL H.
50th European-Renal-Association-European Dialysis and Transplant Association Congress, İstanbul, Türkiye, 18 Mayıs 2013, ss.293
 
ANGIOTENSIN 2 TYPE 1/TYPE 2 GENE POLYMORPHISMS IN TURKISH CHILDREN WITH VESICOURETERAL REFLUX AND RECURRENT URINARY TRACT
BERDELİ A. , EVRENGÜL H., ERTAN P., SAHİN S.
: 50th European-Renal-Association -European-Dialysis-and-Transplant-Association Congress, İstanbul, Türkiye, 18 Mayıs 2013, ss.293
 
RENAL AGENESIS AND HYOPLASIA IN HUMANS ARE NOT ASSOCIATED GLIAL
BERDELİ A. , SERDAROĞLU E., EVRENGÜL H., ERTAN P.
50th European-Renal-Association -European-Dialysis-and-Transplant-Association Congres, İstanbul, Türkiye, 18 Mayıs 2013, ss.317
 
Ciddi enfeksiyon gözlenen sütçocuğunun geçici hipogamaglobülinemisi tanılı hastalarda Fc gamma reseptör polimorfizmi
Azarsız E. , Karaca N. , Tosyalı M., Aksu G. , Berdeli A. , Kütükçüler N.
8. Ulusal Çocuk Allerji, Astım ve Solunum yolu hastalıkları Kongresi, İzmir, Türkiye, 24 Nisan 2013, ss.167-168
 
The place of androgen receptor gene mutation analysis in the molecular diagnosis of prostate cancer and genotype–phenotype relationship
KIZILAY F. , KALEMCİ M. S. , ŞİMŞİR A. , TURNA B. , BERDELİ A. , NAZLI O.
5th Uro-oncology winter congress Skopje, 31 Ocak – 03 Şubat 2013 
 
İlaca bağlı dişeti büyümesi olan böbrek nakli hastalarında FAS, FAS ligand ve IL-6 gen polimorfizmleri
BECERİK S. , GÜRKAN A. , ATİLLA F. G. , BERDELİ A. , EMİNGİL G.
Türk Periodontoloji Dernegi 42. Bilimsel Kongresi, Ankara, Türkiye, 08 Kasım 2012, ss.1
 
TNFRSF13B (TACI), TNFRSF13C (BAFF-R), TNFSF13 (APRIL) GENE MUTATIONS, CTLA-4 AND ICOS GENE POLYMORPHISMS IN TURKISH PATIENTS WITH COMMON VARIABLE IMMUNODEFICIENCY.
BERDELİ A. , GÜLEZ N., KÜTÜKÇÜLER N. , KARACA N. E.
15th Biennial Meeting European-Society-for-Immunodeficiency (ESID), Florence, İtalya, 03 Ekim 2012, ss.269
 
TNFRSF13B (TACI), TNFRSF13C (BAFF-R), TNFSF13 (APRIL) GENE MUTATIONS, CTLA-4 AND ICOS GENE POLYMORPHISMS IN TURKISH PATIENTS WITH COMMON VARIABLE IMMUNODEFICIENCY
KÜTÜKÇÜLER N. , Gulez N. , KARACA N. , AKSU G. , BERDELİ A.
15th Biennial Meeting European-Society-for-Immunodeficiency (ESID), Florence, İtalya, 3 – 06 Ekim 2012, cilt.32, ss.269 identifier
 
IN THE FAMILIAL MEDITERRENEAN FEVER PATIENTS,CARDIOVASKULAR RISK ASSESSMENT GENETIC MARKERS AND BIOMARKERS:LIPOPROTEIN A AND SERUM AMYLOID A
BERDELİ A. , SÖZERİ B., MİR S.
49th Congress of the European Renal Association/European Dialysis and Transplant Association (ERA-EDTA), Paris, Fransa, 24 Mayıs 2012, ss.543
 
THE RELATIONSHIP BETWEEN GLOMERULOSCLEROSIS AND MRNA EXPRESSION OF GENES ENCODING PODOCTYE PROTEINS IN CHILDREN WITH STEROID RESISTAN NEPHROTIC SYNDROME.
BERDELİ A. , SÖZERİ B., MİR M. S.
49th Congress of the European-Renal-Association/European-Dialysis-and-Transplant-Association (ERA-EDTA), Paris, Fransa, 24 Mayıs 2012, ss.543
 
IN THE FAMILIAL MEDITERRENEAN FEVER PATIENTS, CARDIOVASCULAR RISK ASSESSMENT GENETIC MARKERS AND BIOMARKERS: LIPOPROTEIN A AND SERUM AMYLOID A
Sozeri B. , BERDELİ A. , Mir S.
49th Congress of the European-Renal-Association/European-Dialysis-and-Transplant-Association (ERA-EDTA), Paris, Fransa, 24 – 27 Mayıs 2012, cilt.27, ss.543 identifier
 
THE RELATIONSHIP BETWEEN GLOMERULOSCLEROSIS AND MRNA EXPRESSION OF GENES ENCODING PODOCTYE PROTEINS IN CHILDREN WITH STEROID RESISTANT NEPHROTIC SYNDROME.
Dincel N. , BERDELİ A. , Mir S., Akyigit F.
49th Congress of the European-Renal-Association/European-Dialysis-and-Transplant-Association (ERA-EDTA), Paris, Fransa, 24 – 27 Mayıs 2012, cilt.27, ss.538-539 identifier
 
FCGR2C Ailesi Moleküllerinin Hashimoto Tiroiditinde Otoimmunite Oluşumu ile İlişkisi
Mammadova N., Saygılı F., ERDOĞAN M. , Berdeli A.
34 . Ulusal Endokrinoloji ve Metabolizma Kongresi, Antalya, Türkiye, 11 Nisan 2012, ss.1
 
Fas-Fas-L gen polimorfizmi ve Hashimoto tiroiditi gelişimi
ERDOĞAN M. , Ganidağli S., Canataroğlu A., Kösenli A., Kulaksizoğlu M., Çetinkalp Ş. , et al.
33. Türkiye Endokrinoloji ve Metabolizma Hastalıkları Kongresi, Antalya, Türkiye, 12 Ekim 2011, ss.144
 
İnterlökin-6 174 G/C polimorfizmi ve Hashimoto tiroiditi gelişimi
ERDOĞAN M. , Ganidağli S., Canataroğlu A., Kösenli A., Kulaksizoğlu M., Çetinkalp Ş. , et al.
33. Türkiye Endokrinoloji ve Metabolizma Hastalıkları Kongresi, Antalya, Türkiye, 12 Ekim 2011, ss.143
 
DNA Sequence Variants of NPHS2 Gene in 674 Children with SRNS
BERDELİ A. , TİGLİ D., MİR M. S. , ATAN M., DİNCEL N., Nalbantoğlu S.
44th Annual Scientific Meeting of the European Society for Pediatric Nephrology, Dubrovnik, Hırvatistan, 14 Eylül 2011
 
Results of MEFV Gene Full DNA Sequencing Analysis and Genetic Heterogeneity in 3430 Turkish FMF Patients
BERDELİ A. , TİGLİ D., MİR M. S. , ATAN M., Nalbantoğlu S., TOPARLAK P., et al.
44th Annual Scientific Meeting of the European Society for Pediatric Nephrology, Dubrovnik, Hırvatistan, 14 Eylül 2011
 
DNA SEQUENCE ANALYSIS OF MEFV GENE IN 3101 TURKISH PATIENTS CLINICALLY DIAGNOSED WITH FAMILIAL MEDITERRANEAN FEVER.
BERDELİ A. , ATAN M., TOPARLAK P., Nalbantoğlu S., PASOLAR A., TİGLİ D., et al.
THE 4TH INTERNATIONAL CONGRESS OF MOLECULAR MEDICINE, From Cell To Bedside, İstanbul, Türkiye, 27 Haziran 2011, ss.127
 
AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE GENE ‘PKD1’ SEQUENCE VARIATIONS IN TURKISH PATIENTS AND HEALTHY INDIVIDUALS.
BERDELİ A. , SÖZERİ B., DEMİREL İ., MİR M. S. , TOPARLAK P., Nalbantoğlu S.
THE 4TH INTERNATIONAL CONGRESS OF MOLECULAR MEDICINE, From Cell To Bedside, İstanbul, Türkiye, 27 Haziran 2011
 
APOPTOTIC SPECK LIKE PROTEIN mRNA QUANTITATION IN DIFFERENT MEFV MUTATION PROFILES OF FAMILIAL MEDITERRANEAN FEVER PATIENTS
BERDELİ A. , TANYOLAÇ M. B. , Nalbantoğlu S.
THE 4TH INTERNATIONAL CONGRESS OF MOLECULAR MEDICINE, İstanbul, Türkiye, 27 Haziran 2011, ss.208
 
MOLECULAR ANALYSIS IN THE IDENTIFICATION OF THE NOTCH3 GENE SEQUENCE VARIANTS AND GENETIC DIAGNOSTICS.
BERDELİ A. , TİGLİ D., ATAN M., Nalbantoğlu S.
THE 4TH INTERNATIONAL CONGRESS OF MOLECULAR MEDICINE, From Cell To Bedside., İstanbul, Türkiye, 27 Haziran 2011, ss.209
 
Autoinflammation and Components of Intracellular Inflammasome Complex. Book of Abstracts
BERDELİ A. , TANYOLAÇ M. B. , Nalbantoğlu S.
The International Congress on Bioinformatics and Biomics, Aydın, Türkiye, 18 Mayıs 2011, ss.46
 
İnterlökin-6 174 G/C gen polimorfizmi ve diyabetik ayak gelişimi
ERDOĞAN M. , Canataroğlu A., Solmaz S., Kulaksizoğlu M., Çetinkalp Ş. , Özgen A. G. , et al.
47. Ulusal Diyabet Kongresi, Antalya, Türkiye, 11 Mayıs 2011, ss.103 
 
Rekombinaz-Aktivasyon Geni 1’e Bağlı İmmün Yetmezlikler: Genotip-Fenotip Korelasyonu ve BCG Enfeksiyonu
GÜLEZ N., KARACA N. , AZARSIZ E. , AKSU G. , BERDELİ A. , KÜTÜKÇÜLER N.
21. Ulusal İmmünoloji Kongresi, Muğla, Türkiye, 06 Nisan 2011
 
NPHS2 Gene Mutatıon Analysıs Results Of 631 Turkish Patıents Wıth Steroıd Resıstant Nephrotıc Syndrome.
BERDELİ A. , PASOLAR A., TİGLİ D., AKYİĞİT F., DEMİREL İ., ATAN M., et al.
Cell Signal Omics 2011. Integrated Cellular Pathology System Biology of Human Disease, ., Lüksemburg, 26 Ocak 2011, ss.85
 
Mediterranean Fever Gene Mutation Profiling of 3051 Turkish Patients with Periodic Fever
BERDELİ A. , PASOLAR A., TİGLİ D., DEMİREL İ., ATAN M., TOPARLAK P., et al.
Cell Signal Omics 2011, ., Lüksemburg, 26 Ocak 2011, ss.161
 
Urinary UP1b mRNA levels in vesicoureteral reflux and urinary tract infection
KAPLAN BULUT İ. , MİR S., BERDELİ A. , SÖZERİ B.
15th Congress of the International Pediatric Nephrology Association, New-York, Amerika Birleşik Devletleri, 29 Ağustos – 02 Eylül 2010, cilt.25, ss.1913
 
Antimicrobial Peptide LL-37 Protein and mRNA Expressions in Periodontal Diseases
Türkoğlu O., KANDILOGLU G., BERDELİ A. , EMİNGİL G. , ATİLLA F. G.
IADR General Session, Barselona, İspanya, 14 Temmuz 2010, ss.20-0
 
Tip 1 diyabetli hastalarda Fas ve Fas-L gen polimorfizmlerinin değerlendirilmesi
Baydur Şahin S., Çetinkalp Ş. , ERDOĞAN M. , Berdeli A. , Özgen A. G. , Saygılı F., et al.
46. Ulusal Diyabet Kongresi, Antalya, Türkiye, 12 Mayıs 2010, ss.117 
 
Deneysel periodontitiste vazoaktif intestinal peptidin proenflamatuvar ve antienflamatuvar sitokin mRNA ekspresyonlarına etkisi
GÜRKAN A. , EMİNGİL G. , NİZAM N. , BERDELİ A. , ATİLLA F. G.
Periodontoloji Derneği 40. Bilimsel Kongresi, İzmir, Türkiye, 14 – 16 Mayıs 2010
 
Yeni bir mutasyon: Türk toplumunda periodontitis hastalarında CAMP geninin p.S34N mutasyonu
Türkoğlu O., BERDELİ A. , EMİNGİL G. , ATİLLA F. G.
Türk Periodontoloji Dernegi 39.. Bilimsel Kongresi, Ankara, Türkiye, 28 Ekim 2009, ss.3
 
Farklı periodontal hastalıklarda antimikrobiyal peptid katelisidin LL-37 protein ve mRNA ekspresyonunun değerlendirilmesi.
Türkoğlu O., KANDILOGLU G., BERDELİ A. , EMİNGİL G. , ATİLLA F. G.
Türk Periodontoloji Dernegi 39.. Bilimsel Kongresi, Ankara, Türkiye, 28 Ekim 2009, ss.4
 
Associations between PTGS1 gene mutations and aspirin resistance in patients with congenital heart diseases
COSKUN I., Atay Y. , Berdeli A. , MECIDOV M., ATAY A., Ayik M. F. , et al.
34th Congress of the Federation-of-European-Biochemical-Societies, Prague, Çek Cumhuriyeti, 4 – 09 Temmuz 2009, cilt.276, ss.96 identifier
 
The a2 integrin +807 C/T polymorphism in cyclosporine-induced gingival overgrowth
GÜRKAN A. , EMİNGİL G. , AFACAN B., ATİLLA F. G. , TÖZ H. , BERDELİ A.
EUROPERIO 6, Stokholm, Amerika Birleşik Devletleri, 04 Haziran 2009, ss.20
 
The alpha 2 integrin 807 C T polymorphism in cyclosporine induced gingival overgrowth
GÜRKAN A. , EMİNGİL G. , AFACAN B., ATİLLA F. G. , TÖZ H. , BERDELİ A.
Europerio 6, 2009, Stockholm, Sweeden., 4 – 06 Haziran 2009
 
Migraine with Aura; Mutation Analysis of the SLC1A3 Gene
BERDELİ A. , cakir f., idiman f.
61th Annual Meeting of American-Academy-of-Neurology, Seattle, Amerika Birleşik Devletleri, 28 Nisan 2009, ss.176
 
Migraine With Aura Mutation Analysis Of The SLC1A3 Gene Conference Information
BERDELİ A. , idiman f., cakir f.
61st Annual Meeting on American Academy of Neurology, Washington, Amerika Birleşik Devletleri, 17 Mart 2009, ss.176
 
A novel TNFRSF1A Gene Y331X nonsense mutation in two unrelated Turkish families with periodic fever syndrome
BERDELİ A. , KUTUKCULER N. , KARACA N. , GULEZ N.
13th European-Soc for Immunodeficencies/ 10th ınt-patient Org for Primary Immunodeficencies/ 8th ınt-Nursing Group for Immunodeficencies, Hertogenbosch, Hollanda, 16 Ekim 2008, ss.47
 
A mild clinical spectrum of the X-linked lymphoproliferative syndrome in 6-year-old boy:involvement of XIAP/BIRC-4 gene
BERDELİ A. , AKSU G. , GULEZ N., KARACA N.
13th European-Soc-for-Immunodeficiencies/10th Int-Patient-Org-for-Primary-Immunodeficiencies/8th Int-Nursing-Group-for-Immunodeficiencies, Hertogenbosch, Hollanda, 16 Ekim 2008, ss.65
 
TRPC6 mutation in a patient with nephrocalcinosis
BERDELİ A. , KAPLAN BULUT İ. , MİR S., ONDER Y.
42nd Annual ESPN Meeting, Lyon, Fransa, 11 – 14 Eylül 2008, cilt.23, ss.1669 identifier
 
Mutation in the UMOD Gene Responsible for Familial Juvenile Hyperuricemic Nephropaty and Chronic Renal Failure
BERDELİ A. , MUTLUBAS F., MİR M. S. , YAVASCAN O.
42nd Annual ESPN meeting, Lyon, Fransa, 11 Eylül 2008
 
PAX2 ve EYA1 mutations in childhood with familial vesicoureteral reflux
MUTLUBAS F., MİR S., BERDELİ A. , KAPLAN BULUT İ.
42nd Annual ESPN Meeting, Lyon, Fransa, 11 – 14 Eylül 2008, cilt.23, ss.1669
 
New Genetic Non-HLA Markers in Chronic Alloraft Nephropaty
BERDELİ A. , YILMAZ E., MİR M. S.
42nd Annual ESPN meeting, Lyon, Fransa, 11 Eylül 2008
 
Familial vesicoureteral reflux with PAX2/ EYA1 mutation in a Turkish Family
BERDELİ A. , MİR M. S. , ÖZDEMİR R., YILMAZ E.
3rd Europediatrics, İstanbul, Türkiye, 14 Haziran 2008
 
Klinik olarak malignite şüphesi olan tiroid nodüllerinde RET PTC erken dönem sonuçları
UĞUZ A. , GÜRCÜ B., MAKAY Ö. , ERTAN Y. , ÖZGEN A. G. , BERDELİ A. , et al.
Ulusal Cerrahi Kongresi 2008, Türkiye, 28 – 31 Mayıs 2008
 
Can Toll-like resceptor 2 polymorphism affect the phenotype of heterozygous
BERDELİ A. , BAKKALOGLU A., BESBAS N., TOPALOGLU R., ÖZEN S. , AKTAY A., et al.
The 5th International Congress on Familial Mediterranean Fever and Systemic Autoinflamatory Diseases, Rome, İtalya, 04 Nisan 2008
 
Three novel missense amino acid mutations in MEFV gene of Turkish FMF patients
BERDELİ A. , TİGLİ D., ÖZDEMİR N., MİR M. S.
The 5th International Congress on Familial Mediterranean Fever and Systemic Autoinflamatory Diseases, Roma, İtalya, 04 Nisan 2008
 
Polikistik Over Sendromlu Hastalarda Kardiyovasküler Risk Faktörleri ile Fas 670 A/G Gen Polimorfizmi İlişkisi
ERDOĞAN M. , Karadeniz M., Berdeli A. , Tamsel S. , Yılmaz C.
30. Türkiye Endokrinoloji ve Metabolizma Hastalıkları Kongresi, Antalya, Türkiye, 24 Ekim 2007, ss.130
 
Polikistik Over Sendromlu Hastalarda Kardiyovasküler Risk Faktörleri ile İnterlökin-6-174 G/C Gen Polimorfizmi İlişkisi
ERDOĞAN M. , Karadeniz M., Berdeli A. , Tamsel S. , Yılmaz C.
30. Türkiye Endokrinoloji ve Metabolizma Hastalıkları Kongresi, Antalya, Türkiye, 24 Ekim 2007, ss.169
 
Papiller Tiroid Kanserli Hastalarda İnterlökin-10 -1082 G/A ve -819 C/T Gen Polimorfizmi
ERDOĞAN M. , Karadeniz M., Özbek M., Özgen A. G. , Berdeli A.
30. Türkiye Endokrinoloji ve Metabolizma Hastalıkları Kongresi, Antalya, Türkiye, 24 Ekim 2007, ss.116 
 
Polikistik Over Sendromlu Hastalarda Oksidatif Stres Markırları ile İnterlökin-6-174 G/C Gen Polimorfizmi İlişkisi
ERDOĞAN M. , Karadeniz M., Berdeli A. , Alper G., Çağlayan O., Yılmaz C.
30. Türkiye Endokrinoloji ve Metabolizma Hastalıkları Kongresi, Antalya, Türkiye, 24 Ekim 2007, ss.169
 
Renin-angiotensin gene polymorphisms in generalized aggressive periodontitis. I
BERDELİ A. , GÜRKAN A. , EMİNGİL G. , HAN B., ATİLLA F. G. , KÖSE T. , et al.
JOint Meeting Of The Continental European And Israeli Divisions In Thessaloniki, Selanik, Yunanistan, 26 Eylül 2007, ss.20
 
Effect of the MMP-13 genotypes on outcomes of periodontal therapy
PIRHAN D., ATİLLA F. G. , EMİNGİL G. , KÖSE T. , BERDELİ A.
JOint Meeting Of The Continental European And Israeli Divisions In Thessaloniki, Selanik, Yunanistan, 26 Eylül 2007, ss.30
 
Matrix metalloproteinase-2, -9 and -12 polymorphisms in chronic periodontitis
GÜRKAN A. , EMİNGİL G. , HAN B., ATİLLA F. G. , ÇINARCIK S. , KÖSE T. , et al.
JOint Meeting Of The Continental European And Israeli Divisions In Thessaloniki, Selanik, Yunanistan, 26 Eylül 2007, ss.40
 
Renin angiotensin gene polymorphisms in generalized aggressive periodontitis
GÜRKAN A. , EMİNGİL G. , Buket h. S. , Haluk B., ATİLLA F. G. , KÖSE T. , et al.

Annual Meeting IADR-Continental European and Israeli Divisions 2007, Thessaloniki, Greece., 26 – 29 Eylül 2007 identifier identifier identifier 

 
Renin angiotensin gene polymorphisms in chronic periodontitis
GÜRKAN A. , EMİNGİL G. , SAYGAN B. H. , HALUK b., ATİLLA F. G. , KÖSE T. , et al.

Annual Meeting IADR-Continental European and Israeli Divisions 2007, Thessaloniki, Greece., 26 – 29 Eylül 2007 identifier identifier identifier 

 
Matrix metalloproteinase 2 9 and 12 gene polymorphisms in generalized aggressive periodontitis
GÜRKAN A. , EMİNGİL G. , Han B., ATİLLA F. G. , ÇINARCIK S. , KÖSE T. , et al.

Annual Meeting IADR-Continental European and Israeli Divisions, 26 Eylül 2012 – 29 Eylül 2007 identifier identifier identifier 

 
MCP-1, IL 6 and FAS gene polymorphisms and acute renal allograft rejection in children
BERDELİ A. , YILMAZ E., MİR M. S.
44thERA-EDTA Congress, Barcelona, İspanya, 22 Haziran 2007, ss.210
 
Toll like receptor 2 and toll like receptor 4 polymorphisms in children with asthma and allergic rhinitis
Zeyrek D., Tanac R., Demir E., Berdeli A. , Koksoy H., Gulen F., et al.
26th Congress of the European-Academy-of-Allergology-and-Clinical-Immunology, Goteborg, İsveç, 9 – 13 Haziran 2007, cilt.62, ss.380 identifier
 
Tip 2 Diyabetik Nefropatili Hastalarda İnterlökin-10 (1082 G/A) Gen PolimorfizmiGen Polimorfizmi
ERDOĞAN M. , Karadeniz M., Özbek M., Eroğlu Z., Özgen A. G. , Berdeli A.
43. Ulusal Diyabet Kongresi, Antalya, Türkiye, 09 Mayıs 2007, ss.66 
 
Tip 2 Diyabetik Nefropatili Hastalarda Monocyte Chemoattractant Protein 1 (MCP-1) (-2518) A/G Gen Polimorfizmi
ERDOĞAN M. , Özgen A. G. , Karadeniz M., Özbek M., Eroğlu Z., Berdeli A.
43. Ulusal Diyabet Kongresi, Antalya, Türkiye, 09 Mayıs 2007, ss.67 
 
Evaluation of the association of NOD2/CARD15 genotype with clinical course of Turkish Crohn’s disease patients.
TEKİN F. , BERDELİ A. , AYDIN A. , MUSOĞLU A., OSMANOĞLU N., ILTER T.
Falk symphosium, 4 – 05 Mayıs 2007
 
A risk factor secondary amyloidosis in familial mediterranean fever: Arg53Gln TLR-2 polymorphism
BERDELİ A. , TUREL B., OZEN S.
70th Annual Scientific Meeting of the American-College-of-Rheumatology/41th AnnualScientific Meeting of the Association-of-Rheumatology-Healty-Professionals, Washington, Amerika Birleşik Devletleri, 10 Kasım 2006, ss.830
 
Metabolik sendromlu çocuklarda PPAR 2 geninde PRO12 ALA mutasyonu
BERDELİ A. , MİR S., SÖZERİ YENİAY B., YAVASCAN Ö., MUTLUBAS F., KAPLAN BULUT İ.
23. Ulusal Nefroloji, Hipertansiyon, Diyaliz ve Transplantasyon Kongresi, Antalya, Türkiye, 28 Ekim – 01 Kasım 2006, cilt.15, ss.81
 
Primer FSGS tanılı çocuk hastalarda 14 yıllık deneyim
YAVASCAN Ö., YENİAY B. S. , MUTLUBAS F., KAPLAN BULUT İ. , BERDELİ A. , MİR S.
23. Ulusal Nefroloji, Hipertansiyon, Diyaliz ve Transplantasyon Kongresi, Antalya, Türkiye, 28 Ekim – 01 Kasım 2006, cilt.15, ss.81
 
Kronik periodontitiste Matriksmetalloproteinaz -2, -9, -12 Gen Polimorfizmleri.
GÜRKAN A. , EMİNGİL G. , SAYGAN B., ATİLLA F. G. , ÇINARCIK S. , BERDELİ A. , et al.
Türk Periodontoloji Dernegi 36. Bilimsel Kongresi, İzmir, Türkiye, 21 Eylül 2006, ss.4
 
MMP-1 gen polimorfizmi ile şiddetli kronik periodontitis ilişkisi
PIRHAN D., ATİLLA F. G. , EMİNGİL G. , KÖSE T. , BERDELİ A.
Türk Periodontoloji Dernegi 36. Bilimsel Kongresi, İzmir, Türkiye, 21 Eylül 2006, ss.1
 
Toll-like Reseptör 2 ve 4 Gen Polimorfizmleri ile Kronik Periodontitis İlişkisinin Araştırılması
BERDELİ A. , EMİNGİL G. , HAN B., GÜRKAN A. , ATİLLA F. G. , KÖSE T. , et al.
Türk Periodontoloji Dernegi 36. Bilimsel Kongresi, İzmir, Türkiye, 21 Eylül 2006, ss.3
 
Kronik periodontitiste matrismetalloproteinaz 2 9 ve 12 gen polimorfizmleri
GÜRKAN A. , EMİNGİL G. , Buket H. S. , ATİLLA F. G. , ÇINARCIK S. , BERDELİ A. , et al.
Türk Periodontoloji Derneği 36. Bilimsel Kongresi, 2006, Çeşme., Türkiye, 21 – 23 Eylül 2006
 
Kronik periodontitiste TLR 2 ve TLR 4 gen polimorfizmleri
BERDELİ A. , EMİNGİL G. , BUKET H. S. , GÜRKAN A. , ATİLLA F. G. , KÖSE T. , et al.
Türk Periodontoloji Derneği 36. Bilimsel Kongresi, 2006, Çeşme., Türkiye, 21 – 23 Eylül 2006
 
Ege Bölgesinde Papiller Tiroid Karsinomda RET/PTC prevelansı
ERDOĞAN M. , Karadeniz M., Berdeli A. , Tamsel S. , Ertan Y. , Saygılı F., et al.
29. Türkiye Endokrinoloji ve Metabolizma hastalıkları Kongresi, Antalya, Türkiye, 06 Eylül 2006, ss.109
 
Ege Bölgesinde Yaşayan Papiller Tiroid Kanserli Hastalarda Fas-FasL Gen Polimorfizmi
ERDOĞAN M. , Karadeniz M., Berdeli A. , Tamsel S. , Ertan Y. , Uluer H. , et al.
29. Türkiye Endokrinoloji ve Metabolizma hastalıkları Kongresi, Antalya, Türkiye, 06 Eylül 2006, ss.109 
 
A risk factor for secondary amyloidosis in familial mediterranean fever: Arg53Gln TLR-2 polymorphism.
Ozen S., Berdeli A. , Turel B., Kutlay S., Yalcinkaya F., Arici M., et al.
70th Annual Scientific Meeting of the American-College-of-Rheumatology/41st Annual Scientific Meeting of the Association-of-Rheumatology-Health-Professionals, Washington, Kiribati, 10 – 15 Kasım 2006, cilt.54 identifier
 
PPAR-gamma 2 gene Pro12Ala mutation in Turkish children with metabolic syndrome
BERDELİ A. , YENİAY B. S. , MUTLUBAS F.
43rd ERA-EDTA Congress, Glasgow, İskoçya, 15 Temmuz 2006, ss.378
 
TLR4 gene polymorphism in paediatric renal transplantation patients in turkish population
BERDELİ A. , MUTLUBAS F., MİR M. S.
43rd ERA-EDTA Congress, Glasgow, İskoçya, 15 Temmuz 2006, ss.542-543
 
Post-treatment effects of 3-month adjunctive sub-antimicrobial dose doxycycline therapy on clinical parameters and gingival crevicular fluid transforming growth factor-beta1 levels in severe, generalized chronic periodontitis
GÜRKAN A. , EMİNGİL G. , ÇINARCIK S. , BERDELİ A.
euroPerio 5, Madrid, İspanya, 29 Haziran 2006, ss.5
 
RANKL and OPG m RNA expression in CsA treated patients with chronic peiodontitis
İlgenli T., BOSTANCI N., AFACAN B., BELIBASAKIS G. N. , MCKAY I., EMİNGİL G. , et al.
euroPerio 5, Madrid, İspanya, 29 Haziran 2006, ss.20
 
Receptor activator of NF-kappa B ligand and osteoproegerin mRNA expression in periodontal diseases
Bostancı N., İlgenli T., BELIBASAKIS G. N. , HAN B., MCKAY I., EMİNGİL G. , et al.
euroPerio 5, Madrid, İspanya, 29 Haziran 2006, ss.30
 
The association of Tissue Plasminogen Activator and Plasminogen Activator Inhibitor-1 Gene Polymorphisms in Patients with Chronic Periodontitis.
EMİNGİL G. , GÜRKAN A. , ATİLLA F. G. , ÇINARCIK S. , KÖSE T. , BERDELİ A.
euroPerio 5, Madrid, İspanya, 29 Haziran 2006, ss.200
 
The lack of association of toll like receptor 2 and 4 gene polymorphisms with generalized aggressive periodontitis
EMİNGİL G. , BERDELİ A. , HALUK B., HAN B., GÜRKAN A. , KÖSE T. , et al.
Europerio 5, 2006, Madrid, Spain., 29 Haziran – 01 Temmuz 2006
 
Effect of adjunctive low dose doxycycline therapy on clinical parameters and gingival crevicular fluid t PA levels in chronic periodontitis
EMİNGİL G. , GÜRKAN A. , ATİLLA F. G. , BERDELİ A. , ÇINARCIK S.
Europerio 5, 2006, Madrid, Spain., 29 Haziran – 01 Temmuz 2006
 
Gene polymorphisms of tissue plasminogen activator and plasminogen activator inhibitor 1 in patients with generalized aggressive periodontitis
EMİNGİL G. , GÜRKAN A. , BERDELİ A. , han B., KÖSE T. , ATİLLA F. G.

Europerio 5, 2006, Madrid, Spain., 29 Haziran – 01 Temmuz 2006 identifier identifier identifier 

 
TLR2 gene Arg753Glu polymorphism in FMF patients with secondary Amyloidosis
BERDELİ A. , BAKKALOGLU A., ÖZEN S.
EULAR 2006, Amsterdam, Hollanda, 21 Haziran 2006
 
Arg753Gln polymorphism of toll-like receptor 2 gene is increased among fmf patients and in those who develop secondary amyloidosis
BERDELİ A. , YILMAZ E., BESBAS N.
Annual European Congress of Rheumatology (EULAR2006), Amsterdam, Hollanda, 21 Haziran 2006, ss.84
 
Adjunctive low dose doxycycline in severe chronic periodontitis Effect on clinical parameters and crevicular fluid transforming growth factor beta1
GÜRKAN A. , EMİNGİL G. , ÇINARCIK S. , BERDELİ A.
Europerio 5, 2006, Madrid, Spain., 29 Haziran – 01 Temmuz 2006
 
TLR-2 gene ARG753GLN polymorphism is strongly associated with acute rheumatic fever in children
BERDELI A. , Ulger Z. , CELIK H., OZYUREK R., AYDIN H. H.

Annual European Congress of Rheumatology, Vienna, Avusturya, 8 – 11 Haziran 2005, cilt.64, ss.72 identifier identifier identifier 

 

Leukotrienes and atopic bronchial asthma
HUSEYİNOV A. , KURUGÖL Z., DEMİR E.
XVI European Congress of Allergology and Clinical Immunology, Madrid, İspanya, 25 Haziran 2005
 
The vascular endothelial growth factor gene (VEGF) 460 C/T polymorphism in turkish type2 diabetic female patients
BERDELİ A. , DUMAN E., GÜLER K.
65th Annual Meeting of the American-diabetes association, San Diego, Amerika Birleşik Devletleri, 10 Haziran 2005, ss.540-541 
 
Assocation of Glu298Asp Mutation of Endothelial Nitric Oxide Synthase (eNOS) Gene with Turkish Type 2 Diabetic Patients, Nephropathy
BERDELİ A. , YILMAZ C. , DUMAN E., SAYGILI F., GÜLER K.
65th Scientific Sessions American Diabetes Assocation, California, Amerika Birleşik Devletleri, 10 Haziran 2005, ss.209 
 
Intercellular adhesion moleculer-1 (ICAM-1) G241R polymorphism in turkish type2 diabetic female patients
DUMAN E., BERDELİ A. , GÜLER K.
65th Annual Meeting of the American-diabetes association, San Diego, Amerika Birleşik Devletleri, 10 Haziran 2005, ss.540-541 
 
Association of Glu298Asp mutation of endothelial nitric oxide synthase (Enos) gene with Turkish type 2 diabetic patients
DUMAN E., BERDELİ A. , SAYGİLİ F.
65th Annual Meeting of the American-diabetes association, San Diego, Amerika Birleşik Devletleri, 10 Haziran 2005, ss.209 
 
Significance of molecular diagnosis in the cases with suspected
BERDELİ A. , CURA A., OZALKAYA E.
Annual European Congress of Rheumatology, Viyana, Avusturya, 08 Haziran 2005, ss.270
 
RAS gene polymorphisms in primary FSGS and steroid responsive nephrotic syndrome
BERDELİ A. , MİR M. S. , TABEL Y.
42nd Annual Meeting of the European-Renal-Association/European-Dialysis-and-Transplant-Association (ERA-EDTA), İstanbul, Türkiye, 04 Haziran 2005, ss.32
 
ICAM-1 gene 142R allele is not asociated with rejection in pediatric kidney transplantation
BERDELİ A. , KABASAKAL S. C. , ERGOR S.
42nd Annual Meeting of the European-Renal-Association/European-Dialysis-and-Transplant-Association (ERA-EDTA), İstanbul, Türkiye, 04 Haziran 2005, ss.180
 
The evaluation of molecular diagnosis in cases with FMF
BERDELİ A. , CURA A., OZALKAYA E.
42nd Annual Meeting of the European-Renal-Association/European-Dialysis-and-Transplant-Association (ERA-EDTA), İstanbul, Türkiye, 04 Haziran 2005, ss.192
 
Triple homozygous podocin mutations in a patient with familial congenital focal segmental glomerulosclerosis associated with cardiac malformation
BERDELİ A. , SONMEZ F., MİR M. S.
42nd Annual Meeting of the European-Renal-Association/European-Dialysis-and-Transplant-Association (ERA-EDTA), İstanbul, Türkiye, 04 Haziran 2005, ss.226
 
TNF-? -308 G/A Promoter Polymorhism in Turkish Morbidly Obese Patients
BERDELİ A. , OZGEN A. G. , YILMAZ C. , DUMAN E., SAYGILI F., GÜLER K., et al.
ENDO 2005: 87th Annual Meeting, California, Amerika Birleşik Devletleri, 04 Haziran 2005, ss.233
 
Fc gamma receptor polymorphisms: Can be a risk factor for urinary tract infections
BERDELİ A. , TABEL Y., OZDEMİR R.
42nd Annual Meeting of the European-Renal-Association/European-Dialysis-and-Transplant-Association (ERA-EDTA), İstanbul, Türkiye, 04 Haziran 2005, ss.32
 
TLR gene mutations in children with urinary tract infection
BERDELİ A. , MİR M. S. , TABEL Y.
42nd Annual Meeting of the European-Renal-Association/European-Dialysis-and-Transplant-Association (ERA-EDTA), İstanbul, Türkiye, 04 Haziran 2005, ss.33
 
Periodontal hastalıklarda endotelyalnitrik oksit sentaz (eNOS) Glu298Aspl gen polimorfizmi
BERDELİ A. , GÜRKAN A. , EMİNGİL G. , ATİLLA F. G. , KÖSE T.
Türk Periodontoloji Dernegi 35. Bilimsel Kongresi, İstanbul, Türkiye, 12 Mayıs 2005, ss.3
 
Periodontal hastalıklarda transforme edici büyüme aktörü-beta1 gen polimorfizmleri
ATİLLA F. G. , EMİNGİL G. , BERDELİ A. , KÖSE T.
Türk Periodontoloji Dernegi 35. Bilimsel Kongresi, İstanbul, Türkiye, 12 Mayıs 2005, ss.1
 
İnterlökin 1 reseptör antagonist geninin periodontal hastalık ile pozitif ilişkisi
BERDELİ A. , EMİNGİL G. , GÜRKAN A. , ATİLLA F. G. , KÖSE T.
Periodontoloji Derneği 35. Bilimsel Kongresi, 2005, İstanbul., Türkiye, 12 – 14 Mayıs 2005
 
Periodontal hastalıklarda endotelyal nitrik oksit sentaz eNOS Glu298Asp gen polimorfizmi
BERDELİ A. , GÜRKAN A. , EMİNGİL G. , ATİLLA F. G. , KÖSE T.
Periodontoloji Derneği 35. Bilimsel Kongresi, 2005, İstanbul., Türkiye, 12 – 14 Mayıs 2005
 
The paraoxonase gene M/L55 and Q/R192 polymorphisms are not associated with coronary artery disease and response to atorvastatin
BERDELİ A. , SİRRİ C. F. , ŞEKURİ C.
75th Congress of the European-Atherosclerosis-Society, Prague, Çek Cumhuriyeti, 23 Nisan 2005, ss.20
 
TLR2 gene Arg753Gln mutation associated with urinary tract infection in children
BERDELİ A. , TABEL Y., MİR M. S.
19th European Immunogenetics and Histocompatibility Conference, İstanbul, Türkiye, 23 Nisan 2005, ss.12
 
Positive association of FcgRIIa-131R and FcgRIIIb-NA2 allele with urinary tract infection in children
ÖZDEMİR R., BERDELİ A. , TABEL Y.
19th European Immunogenetics and Histocompatibility Conference, İstanbul, Türkiye, 23 Nisan 2005, ss.18
 
No association of IL-6 gene polymorphism (474/G/C) with premature coronary artery disease
ŞEKURİ C., SİRRİ C. F. , TENGİZ İ., BERDELİ A.
75th Congress of the European-Atherosclerosis-Society, Prague, Çek Cumhuriyeti, 23 Nisan 2005, ss.89
 
Influence Of Patient and Donor Gene Polymorphism On Renal Allograft Rejection: Evidence From Single Center Study
BERDELİ A. , CURA A., MUTLUBAS F., MİR M. S. , OZKAYIN N., ERTAN P., et al.
19th European Immunogenetics & Histocompatibility Conference, İstanbul, Türkiye, 23 Nisan 2005, ss.205
 
Influence of patient and donor gene polymorphism on renal allograft rejection: Evidence from a single center study
Berdeli M. , Ertan P., Ozkayin N., Kabasakal C., Mutlubas F.
19th European Immunogenetics and Histocompatibility Conference, İstanbul, Türkiye, 23 – 26 Nisan 2005, cilt.6 identifier
 
Transforming growth factor beta1 gene polymorphisms in periodontal diseases.
ATİLLA F. G. , EMİNGİL G. , KÖSE T. , BERDELİ A.
IADR General Session, Baltimore, Amerika Birleşik Devletleri, 09 Mart 2005, ss.10
 
Crevicular Fluid EMAP-II, MIP-1alpha and MIP-1beta Levels in Periodontal Disease
EMİNGİL G. , ATİLLA F. G. , BASKESEN A., BERDELİ A.
IADR General Session, Baltimore, Amerika Birleşik Devletleri, 09 Mart 2005, ss.25
 
The positive association of IL-1RN2 allele with periodontal disease
BERDELİ A. , EMİNGİL G. , GÜRKAN A. , ATİLLA F. G. , KÖSE T.
IADR General Session, Baltimore, Amerika Birleşik Devletleri, 09 Mart 2005, ss.20
 
Endothelial nitric oxide synthase Glu298Asp gene polymorphism in periodontal disease
BERDELİ A. , GÜRKAN A. , EMİNGİL G. , ATİLLA F. G. , KÖSE T.
IADR/AADR/CADR 83rd General Session, March 9-12, 2005, Baltimore, USA., 9 – 12 Mart 2005
 
Intercellular adhesion molecule-1 (ICAM-1) G241R polymorphism in Turkish type 2 diabetic female patients
Duman E., Berdeli A. , Guler K., Saygili F., Yilmaz C.
65th Annual Meeting of the American-Diabetes-Association, California, Amerika Birleşik Devletleri, 10 – 14 Haziran 2005, cilt.54  identifier
 
Ace DD Genotipi Dayanıklılık Performansı İle İlişkili Mi ?
ÇAM F. S. , ÇOLAKOĞLU B. M. , AKŞİT T., ÖZKOL M. Z. , BERDELİ A.
10.ICHPER-SD Avrupa Kongresi ve Uluslararası Spor Bilimleri Kongresi, Antalya, Türkiye, 17 – 20 Kasım 2004, ss.44
 
Is the Ace DD Genotype Associated Wıth A eter Endurance Performance?
BERDELİ A. , ÇAM F. S. , COLAKOGLU M., COLAKOGLU S., AKŞİT T. , ÖZKOL M. Z.
X.ICHPER-SD Avrupa ve 8. Uluslararası Spor Bilimleri Kongresi, Antalya, Türkiye, 18 Kasım 2004
 
Association of polymorphism in the IL-6 gene with morbid obesity
BERDELİ A. , ÖZGEN A. G. , YILMAZ C. , DUMAN E., SAYGILI F., GÜLER K., et al.
12th International Congress of Endocrinology, Lizbon, Portekiz, 31 Ağustos 2004 
 
Effect of the Asp298 variant of endothelial nitric oxide synthase on patients with early coronary artery disease in a Turkish population, European Heart Journal
BERDELİ A. , SEKURI C., ERCAN E., ÇAM F. S. , ABDİ S.
ESC Congress 2004, Münih, Almanya, 28 Ağustos 2004
 
Effect of the asp298 variant of endothelial nitric oxide synthase on patients with early coronary artery disease in a turkish population
BERDELİ A. , SİRRİ C. F. , ŞEKURİ C., ERCAN E.
ESC Congress 2004, Munich, Almanya, 28 Ağustos 2004, ss.106
 
Gingival crevicular fluid TGF ß1 levels in spesific periodontal diseases
GÜRKAN A. , EMİNGİL G. , ÇINARCIK S. , BERDELİ A.
Joint Meeting of the Continental European Division (CED), Scandinavian Division (NOF) and Israeli Division (ID) of IADR, 2004, İstanbul., 19 – 29 Ağustos 2004
 
Positive Correlation Between A-173-MIF*C Allele Polymorphism of Macrophage Migration Inhibitory Factor and Steroid Resistance In Children With Nephrotic Syndrome
BERDELİ A. , CURA A., SERDAROGLU E., MİR M. S. , OZKAYIN N.
XLI. Congress of the European Renal Association, European Dialysis and Transplant Association, Lizbon, Portekiz, 15 Mayıs 2004
 
Kronik periodontitisin cerrahisiz tedavisine ek olarak kullanılan düşük doz doksisiklinin klinik parametrelere ve dişeti oluğu sıvısı TGF ß1 seviyesine etkisi
GÜRKAN A. , ÇINARCIK S. , BERDELİ A.
Türk Periodontoloji Derneği 34.Kongresi, 2004, Ankara., Türkiye, 29 Nisan – 02 Mayıs 2004
 
Association between Renin-Angiotensin System Gene Polymorphisms and Premature Coronary Heart Disease in a Turkish Population, Atherosclerosis Suppl
BERDELİ A. , SEKURİ C., ERCAN E., ÇAM F. S. , ABDİ S.
74th EAS Congress, Sevilla, İspanya, 17 Nisan 2004
 
Association between renin-angiotensin system gene polymorphisms and premature coronary heart disease in a turkish population.
BERDELİ A. , SİRRİ C. F. , ŞEKURİ C., ERCAN E.
74th Congress of the european atherosclerosis society, Seville, İspanya, 17 Nisan 2004, ss.90
 
Positive association of A-173-MIF*C allele polymorphism of macrophage migration inhibitory factor and steroid resistant in children with nephrotic syndrome
BERDELİ A. , CURA A., SERDAROGLU E., MİR M. S. , OZKAYIN N., TABEL Y.
International Pediatric Nephrology Association, 7th Symposium on Growth and Development in Children with Chronic Kidney Disease: The Molecular Basis of Skeletal Growth, Heidelberg, Almanya, 01 Nisan 2004
 
Podocin (NPHS2) gene mutation in Turkish children with steroid resistant nephrotic syndrome
BERDELİ A. , CURA A., SERDAROGLU E., MİR M. S. , OZKAYIN N., TABEL Y.
International Pediatric Nephrology Association, 7th Symposium on Growth and Development in Children with Chronic Kidney Disease: The Molecular Basis of Skeletal Growth, Heidelberg, Almanya, 01 Nisan 2004
 
Enhanced production of platelet activating factor by leucocytes from asthmatic children.
HUSEYİNOV A. , DEMİR E., KURUGÖL Z.
XVI EUROPEAN CONGRESS OF ALLERGOLOGY AND CLINICAL IMMUNOLOGY, Madrid, İspanya, 25 Haziran 1995, ss.443-448
 
leukotrienes and PAF release in children with atopic bronchial asthma
BERDELİ A. , Svyatkina O., Pogomi N., Veltişev Y.
Interasthma. 93. XIV World Congress of Asthmology, Tel-Aviv, İsrail, 24 Ekim 1993
 
the detection of lipoxygenase metabolites of arachidonic acid in urine in children with ABA
BERDELİ A. , Svyatkina O., Veltişev Y., Pogomi N., Tanaç R.
nterasthma. 93. XIV World Congress of Asthmology, Tel-Aviv, İsrail, 24 Ekim 1993
 
HPLC Technique for determination of PAF İn Biological Media
BERDELİ A. , TANELİ B., ARCASOY M., MİR M. S.
Application of HPLCand CE in Biosciences, Verona, İtalya, 07 Eylül 1993
 
The Detection Of Released And Cell Associated Lts From Leukocytes İn Vitro After Different Stimulation
BERDELİ A. , TANELİ B., MİR M. S.
22nd Meeting Of The Federation Of Biochemical Societies, Stocholm, İsveç, 04 Temmuz 1993
 
Methods Pointing To The Role Of Xenobiotics İn Producing The Allergic Disease
BERDELİ A. , TANELİ B.
Nato Advanced Study İnstitute Of Molecular Aspect Of Oxydative Drug; Metabolizing Enzymes Their Significance İn Environmental Toxicology, Aydın, Türkiye, 20 Haziran 1993
 
The Release Of Leukotrienes From Blood Leukocytes Under Effect Of The Platelet Activating Factor İn Vitro İn Children With Glomerulonephritis
BERDELİ A. , Ignatova M., Svyatkina O., Kharina L., Veltişev Y.
The Ninth Congress Of The İnternational Pediatric Nephrology Association, Jerusalem, İsrail, 30 Ağustos 1992
 
Hidroxyeicozatetraenoic Acids (HETE’s) in Urine of Children With Glomerulonephritis
BERDELİ A. , Svyatkina O., Kharina L., İgnatova M., Veltişev Y.
The Ninth Congress of The İnternational Pediatric Nephology Association, Jerusalem, İsrail, 30 Ağustos 1992
 
The Role Of Lts İn Children With İmmunocomplex Glomerulonephritis
BERDELİ A. , Svyatkina O., MİR M. S.
Annual Meeting Of The European Academy Of Allergy And Clinical İmmunology, Hollanda
 
The New Lipid Mediators of Inflammation in Children with Glomerulonephritis
BERDELİ A. , MİR M. S. , İgnatova M., Svyatkina O., Kharina L., Veltişev Y.
XXI Congress of Union of Middle Eastern and Mediterranean Pediatric Societies, İzmir, Türkiye
 
Molecular Analysis of CFTR Gene Sequence Variation Profiles in Turkish Cystic Fibrosis Patients
BERDELİ A. , TİGLİ D., DEMİREL İ., ATAN M., TOPARLAK P., Nalbantoğlu S.
The International Congress on Bioinformatics and Biomics,, Aydın, Türkiye, ss.47
 
FC?R II a , IIIa and IIIb polymorphism in Turkish children susceptible to infectious diseases
BERDELİ A. , OZTURK C., AKSU G. , KÜTÜKÇÜLER N.
XI. Meeting for the European Society for Immunodeficies, Fransa, ss.66 
 
The Role of Lipid Mediators In The Development Of Different Inflammatory Reaction In Children
BERDELİ A. , Svyatkina O., Pogoni N., Veltişev Y.
Annual Meeting Of The European Academy And Clinical Immunology, Hollanda
 
the new lipid mediators of allergy and atopic bronchial asthma in children
BERDELİ A. , Svyatkina O., Pogomi N., Arcasoy M., Veltişev Y.
XXI Congress of Union of Middle Eastern and Mediterranean Pediatric Societies,, İzmir, Türkiye
 
Role of Leukotrienes and Platelet Activating Factor in Development of Various Types of Inflammatory Reaction in Children
BERDELİ A. , Svyatkina O., Pogomi N., TANELİ B., Arcasoy M., MİR M. S.
Congress of Union of Middle Eastern and Mediterranean Pediatric Societies, İzmir, Türkiye
 
Podocyte Biology and Nephrotic Syndrome.
BERDELİ A. , PASOLAR A., TİGLİ D., DEMİREL İ., ATAN M., MİR M. S. , et al.
The International Congress on Bioinformatics and Biomics, Aydın, Türkiye, ss.48