Doğa Türkkahraman

Sağlık Bilimleri University - İstanbul / Türkiye

Medical and Health Sciences / Pediatric Endocrinology and Metabolism

AD Scientific Index ID: 182439

University of Health Sciences, Turkey Sağlık Bilimleri Üniversitesi SBU

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Doğa Türkkahraman's MOST POPULAR ARTICLES

1-) Wolcott-Rallison syndrome is the most common genetic cause of permanent neonatal diabetes in consanguineous familiesO Rubio-Cabezas, AM Patch, JAL Minton, SE Flanagan, EL Edghill, ...The Journal of Clinical Endocrinology & Metabolism 94 (11), 4162-4170, 20091522009

2-) Prevalence and risk factors of obesity in school children in Antalya, Turkey.D Turkkahraman, I Bircan, O Tosun, O Sakaadolescence 1, 2, 2006652006

3-) Permanent neonatal diabetes mellitus caused by a novel homozygous (T168A) glucokinase (GCK) mutation: initial response to oral sulphonylurea therapyD Turkkahraman, I Bircan, ND Tribble, S Akçurin, S Ellard, AL GloynThe Journal of pediatrics 153 (1), 122-126, 2008642008

4-) Successful granulocyte colony-stimulating factor treatment of relapsing Candida albicans meningoencephalitis caused by CARD9 deficiencyF Celmeli, N Oztoprak, D Turkkahraman, D Seyman, E Mutlu, N Frede, ...The Pediatric infectious disease journal 35 (4), 428-431, 2016592016

5-) Phenotypic severity of homozygous GCK mutations causing neonatal or childhood-onset diabetes is primarily mediated through effects on protein stabilityA Raimondo, AJ Chakera, SK Thomsen, K Colclough, A Barrett, ...Human molecular genetics 23 (24), 6432-6440, 2014592014

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