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IDENTIFICATION OF THE MUTATION IN DCLRE1C GENE BY PCR-RFLP

MEHMET ALİ KARASELEK, SERKAN KÜÇÜKTÜRK, HASAN KAPAKLI, ESRA HAZAR, ŞÜKRÜ NAIL GÜNER, SEVGI KELEŞ, ERCAN KURAR, İSMAIL REISLI

IDENTIFICATION OF THE MUTATION IN DCLRE1C GENE BY PCR-RFLP

MEHMET ALİ KARASELEK, SERKAN KÜÇÜKTÜRK, HASAN KAPAKLI, ESRA HAZAR, ŞÜKRÜ NAIL GÜNER, SEVGI KELEŞ, ERCAN KURAR, İSMAIL REISLI

TWO CHILDREN ADMITTED WITH HYPOKALEMIA: FAMILIAL GITELMAN SYNDROME

ALİ KARAGÖZ, HARUN PERU, ŞEVKET ARSLAN, İBRAHİM GÜNEY, LÜTFULLAH ALTINTEPE

A RARE MUTATION IN ANDROGEN RECEPTOR GENE WITH A CASE OF PRIMARY AMENORRHOEA

MAKBULE NİHAN SOMUNCU, AYŞE GÜL ZAMANİ, EMİNE GÖKTAŞ, SELMAN YILDIRIM, KAZIM GEZGİNÇ

A RARE MUTATION IN ANDROGEN RECEPTOR GENE WITH A CASE OF PRIMARY AMENORRHOEA

MAKBULE NİHAN SOMUNCU, AYŞE GÜL ZAMANİ, EMİNE GÖKTAŞ, SELMAN YILDIRIM, KAZIM GEZGİNÇ

CORRELATION BETWEEN BRAFV600E POSITIVE AND RECURRENCE AND POOR PROGNOSIS IN PREOPERATIVE FINE NEEDLE ASPIRATION BIOPSY OF PAPILLARY THYROID CARCINOMA

SELMAN ALKAN, FARUK AKSOY, ARSLAN HASAN KOCAMAZ, MUSTAFA ŞENTÜRK, ALPER VARMAN, SIDIKA FINDIK, MAHMUT SELMAN YILDIRIM, ÖMER KİŞİ, CELALETTİN VATANSEV

COMPARISON OF THE TWO LIPOPROTEIN APHERESIS METHODS IN THE TREATMENT OF FAMILIAL HYPERCHOLESTEROLEMIA

ÖZCAN ÇENELİ, MEHMET ALİ KARASELEK, ATAKAN TEKİNALP, SİNAN DEMİRCİOĞLU, MUSTAFA KULAKSIZOĞLU

THE EVELUATION OF CYSTIC FIBROSIS FREQUENCY IN CHILDREN WITH MALNUTRITION AND/ OR RECURRENT PULMONARY INFECTION

YAŞAR CESUR, MURAT DOĞAN, SEVİL ARI YUCA, ERDAL PEKER, MESUT OKUR, SİNAN AKBAYRAM, ŞEKİBE ZEHRA DOĞAN

THE NUTRITION AND CANCER

ÖMER KARAHAN, YÜKSEL TATKAN, SERDAR YOL

ACHONDROPLASIA: A CASE REPORT

MEHMET EMRE ATABEK, KÜRŞAD AYDIN, BÜLENT ORAN, İBRAHIM ERKUL

A CASE REPORT OF NEUROFIBROMATOSIS TYPE 1 DIAGNOSED WITH A NOVAL MUTATION DETECTION IN NF1 GENE

NAFİZ YAŞA, BÜŞRA ESER ÇAVDARTEPE, FAHRETTİN DUYMUŞ, NADİR KOÇAK, TÜLİN ÇORA