Siblings with Ethylmalonic Encephalopathy: Case Report by Çiğdem Seher Kasapkara, Ayşe Aksoy, Emine Polat, Mustafa Kılıç, Serdar Ceylaner

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Hypercalcemia in glycogen storage disease type I patients of Turkish origin by Ciğdem Seher Kasapkara, Leyla Tümer, Ilyas Okur, Tuba Eminoğlu, Fatih Süheyl Ezgü, Alev Hasanoğlu

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An infant with an extremely rare cobalamin disorder: Methionine synthase deficiency and importance of early diagnosis and treatment by Çiğdem Seher Kasapkara, Ebru Yılmaz-Keskin, Ferda Özbay-Hoşnut, Meltem Akçaboy, Emine Polat, Asburçe Olgaç, Pelin Zorlu

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The First Case of 4H Syndrome with Type 1 Diabetes Mellitus by Gönül Büyükyılmaz, Büşra Erozan Çavdarlı, Keziban Toksoy Adıgüzel, Mehmet Adıgüzel, Çiğdem Seher Kasapkara, Fatih Gürbüz, Mehmet Boyraz, Esra Gürkaş

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Novel sphingosine-1-phosphate lyase mutation causes multisystemic diseases: case report by Gönül Büyükyılmaz, Keziban Toksoy Adıgüzel, Özlem Yüksel Aksoy, Çiğdem Seher Kasapkara, Gizem Ürel Demir, Engin Demir, Şule Berk Ergun, Fatih Gürbüz, Mehmet Boyraz

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