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American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 26, 2004
Infantile steroid-resistant nephrotic syndrome associated with double homozygous mutations of podocinGianluca Caridi, Afig Berdeli, Monica Dagnino, et al.
Pediatric Nephrology (Berlin, Germany)|March 29, 2006
Alterations of blood pressure in type 1 diabetic children and adolescentsSukran Darcan, Damla Goksen, Sevgi Mir, et al.
Anadolu Kardiyoloji Dergisi : AKD = the Anatolian Journal of Cardiology|October 14, 2008
G protein beta3 subunit gene polymorphism in Turkish hypertensivesEmin Alioğlu, Ertuğrul Ercan, Istemihan Tengiz, et al.
Renal Failure|February 26, 2014
Val2Ala mutation in the Atp6v0a4 gene causes early-onset sensorineural hearing loss in children with recessive distal renal tubular acidosis: a case reportEngin Kose, Seda Sirin Kose, Caner Alparslan, et al.
Annals of Hepatology|June 9, 2009
Common SPINK-1 mutations do not predispose to the development of non-alcoholic fatty liver diseaseNevin Oruc, Omer Ozutemiz, Afig Berdeli, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 7, 2022
Long-term follow-up of alkaptonuria patients: single center experienceAyse Ergul Bozaci, Havva Yazici, Ebru Canda, et al.
Turkish Journal of Medical Sciences|December 14, 2020
Demographic and clinical characteristics of children with autosomal dominant polycystic kidney disease: a single center experienceBelde Kasap Demir, Fatma Mutlubaş, Eren Soyaltın, et al.
Journal of Periodontology|September 27, 2019
Differential expression of inflammasome regulatory transcripts in periodontal diseaseKübra Aral, Eynar Berdeli, Paul Roy Cooper, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|August 6, 2013
Escherichia coli brain abscess in a twin pair associated with TLR4 gene mutationAydin Erdemir, Zelal Kahramaner, Hese Cosar, et al.
Clinical Case Reports|May 3, 2021
Four diseases, PLAID, APLAID, FCAS3 and CVID and one gene (PHOSPHOLIPASE C, GAMMA-2; <i>PLCG2</i>): Striking clinical phenotypic overlap and differenceNecil Kutukculer, Ezgi Topyildiz, Afig Berdeli, et al.
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