A Rare Leukoencephalopathy: Succinate Dehydrogenase Deficiency

by Özdem Ertürk Çetin, Tanyel Zubarioglu, Cengiz Yalçınkaya
Published 2017-06-01

Early Diagnosis of Fanconi-Bickel Syndrome and a Novel Mutation inSLC2A2 Gene

by Ezgi Çelikboya, Mehmet Şerif Cansever, Tanyel Zübarioğlu, Gözde Yeşil, Nurver Akıncı
Published 2019-09-01

The impact of continuous renal replacement therapy for metabolic disorders in infants

by Fatih Aygun, Deniz Aygun, Firuze Erbek Alp, Tanyel Zubarıoglu, Cigdem Zeybek, Halit Cam
Published 2018-02-01

İdrarda Orotik Asit’in Temassız İletkenlik Dedektörü Kullanılarak Kapiler Elektroforez Yöntemi İle Hızlı Tayini

by Mehmet Şerif Cansever, Veselina Adımcılar, Ayşe Aktuğlu, Ertuğrul Kıykım, Tanyel Zübarioğlu, Nevin Öztekin
Published 2020-11-01

Long-term N-carbamylglutamate treatment of hyperammonemia in patients with classic organic acidemias

by Ertugrul Kiykim, Ozge Oguz, Cisem Duman, Tanyel Zubarioglu, Mehmet Serif Cansever, Ayse Cigdem Aktuglu Zeybek
Published 2021-03-01

Clinical and neuroradiological approach to fucosidosis in a child with atypical presentation

by Tanyel Zubarioglu, Ertugrul Kiykim, Cigdem Aktuglu Zeybek, Mehmet Serif Cansever, Gulcin Benbir, Ahmet Aydin, Cengiz Yalcinkaya
Published 2015-01-01

Expert opinion on diagnosing, treating and managing patients with cerebrotendinous xanthomatosis (CTX): a modified Delphi study

by Bianca M. L. Stelten, Maria Teresa Dotti, Aad Verrips, Bülent Elibol, Tzipora C. Falik-Zaccai, Kate Hanman, Andrea Mignarri, Belina Sithole, Robert D. Steiner, Surabhi Verma, Gilad Yahalom, Tanyel Zubarioglu, Fanny Mochel, Antonio Federico
Published 2021-08-01