Metreleptin Treatment in a Boy with Congenital Generalized Lipodystrophy due to Homozygous c.465_468delGACT (p.T156Rfs8) Mutation in the BSCL2 Gene: Results From the First-year von Ozalkak, Servan, Demiral, Meliha, Unal, Edip, Tas, Funda Feryal, Onay, Huseyin, Demirbilek, Huseyin, Ozbek, Mehmet Nuri

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Aromatase Deficiency due to a Novel Mutation in CYP19A1 Gene von Unal, Edip, Yıldırım, Ruken, Taş, Funda Feryal, Demir, Vasfiye, Onay, Hüseyin, Haspolat, Yusuf Kenan

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Revisiting the Annual Incidence of Type 1 Diabetes Mellitus in Children from the Southeastern Anatolian Region of Turkey: A Regional Report von Özalkak, Şervan, Yıldırım, Ruken, Tunç, Selma, Ünal, Edip, Taş, Funda Feryal, Demirbilek, Hüseyin, Özbek, Mehmet Nuri

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The clinical and laboratory features of patients with triple A syndrome: a single-center experience in Turkey von Yıldırım, Ruken, Unal, Edip, Tekmenuray-Unal, Aysel, Taş, Funda Feryal, Özalkak, Şervan, Çayır, Atilla, Özbek, Mehmet Nuri

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Cytochrome P450 oxidoreductase deficiency caused by a novel mutation in the POR gene in two siblings: case report and literature review von Unal, Edip, Demiral, Meliha, Yıldırım, Ruken, Taş, Funda Feryal, Ceylaner, Serdar, Özbek, Mehmet Nuri

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Unusual cause of hyperammonemia in two cases with short-term and long-term valproate therapy successfully treated by single dose carglumic acid von Kasapkara, Ciğdem Seher, Kanğın, Murat, Taş, Funda Feryal, Topçu, Yasemin, Demir, Remezan, Ozbek, Mehmet Nuri

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Evaluation and management of neonatal onset hyperinsulinemic hypoglycemia: a single neonatal center experience von Bezirganoglu, Handan, Okur, Nilufer, Celik, Kiymet, Tas, Funda Feryal, Ozbek, Mehmet Nuri

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A rare cause of neonatal hypoglycemia in two siblings: TBX19 gene mutation von Unal, Edip, Yıldırım, Ruken, Taş, Funda Feryal, Tekin, Suat, Sen, Askin, Haspolat, Yusuf Kenan

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Retrospective Analysis of Demographic, Epidemiologic, and Clinical Characteristics of Poisoning Cases Followed in Pediatric Intensive Care Unit von Ödek, Çağlar, Akça, Halise, Erol, Mehmet, Demir, Remezan, Tunç, Melek, Aydınalp, Ahmet, Feryal Taş, Funda, Samancı, Serhat

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Demograpghic and Epidemiological Characteristics of Subacute Sclerosing Panencephalitis Patients in Pediatric Intensive Care Unit and Attitudes of Their Parents About Home Care von Ödek, Çağlar, Erol, Mehmet, Demir, Remezan, Tunç, Melek, Aydınalp, Ahmet, Taş, Funda Feryal, Köşker, Muhammet, Samancı, Serhat

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Retrospective Analysis of Demographic, Epidemiologic, and Clinical Characteristics of Poisoning Cases Followed in Pediatric Intensive Care Unit von Ödek, Çağlar, Erol, Mehmet, Demir, Remezan, Tunç, Melek, Aydınalp, Ahmet, Taş, Funda Feryal, Samancı, Serhat

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Çocuk yoğun bakım ünitesinde takip edilen zehirlenme olgularının demografik, epidemiyolojik ve klinik özelliklerinin geriye dönük değerlendirilmesi von Ödek,Çağlar, Akça,Halise, Erol,Mehmet, Demir,Remezan, Tunç,Melek, Aydınalp,Ahmet, Taş,Funda Feryal, Samancı ,Serhat

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Çocuk yoğun bakım ünitesinde izlenen subakut sklerozan panensefalit olgularının demografik, epidemiyolojik özellikleri ve ailelerinin evde bakım konusundaki tutumları von Ödek,Çağlar, Erol,Mehmet, Demir,Remezan, Tunç,Melek, Aydınalp,Ahmet, Taş,Funda Feryal, Köşker,Muhammet, Samancı ,Serhat

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Transient neonatal diabetes mellitus caused by a novel mutation in the ABCC8 gene von Unal, Edip, Yıldırım, Ruken, Taş, Funda Feryal, Yıldız, Süleyman, Demir, Vasfiye, Haspolat, Yusuf kenan

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Unusual cause of hyperammonemia in two cases with short-term and long-term valproate therapy successfully treated by single dose carglumic acid von Kasapkara, Ciğdem Seher, Kanğın, Murat, Taş, Funda Feryal, Topçu, Yasemin, Demir, Remezan, Ozbek, Mehmet Nuri

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