Empagliflozin for treating neutropenia and neutrophil dysfunction in 21 infants with glycogen storage disease 1b von Grünert, Sarah C., Gautschi, Matthias, Baker, Joshua, Boyer, Monica, Burlina, Alberto, Casswall, Thomas, Corpeleijn, Willemijn, Çıki, Kismet, Cotter, Melanie, Crushell, Ellen, Derks, Terry G.J., Haas, Dorothea, Kilavuz, Sebile, Kingma, Sandra D.K., Korman, Stanley H., Kozek, Anne, de Laet, Corinne, Mundy, Helen, Nassogne, Marie Cecile, Quintero, Victor, Rossi, Alessandro, Spenger, Johannes, Spiegel, Ronen, Stephenne, Xavier, Stojkov, Darko, Tal, Galit, Veiga-da Cunha, Maria, Wortmann, Saskia B.

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Single Institutional Experience with GM1 Gangliosidosis: Clinical and Laboratory Results of 14 Patients von Akar, Halil Tuna, Yıldız, Yılmaz, Güvenkaya, Gökhan, Çıkı, Kısmet, Kahraman, Ayça Burcu, Erdal, İzzet, Coşkun, Turgay, Dursun, Ali, Sivri, Hatice Serap, Tokatlı, Ayşegül

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COVID-19-related anxiety in phenylketonuria patients von Akar, Halil Tuna, Karaboncuk, Yamac, ciki, Kismet, Kahraman, Ayca Burcu, Erdal, Izzet, Coskun, Turgay, Tokatli, Aysegul, Dursun, Ali, Yildiz, Yilmaz, Sivri, H. Serap

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Novel Mutation in the HSD17B10 Gene Accompanied by Dysmorphic Findings in Female Patients von Ciki, Kismet, Alavanda, Ceren, Kara, Murat

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DNAJC12 deficiency in patients with unexplained hyperphenylalaninemia: two new patients and a novel variant (May, 10.1007/s11011-021-00753-0, 2021) von ciki, Kismet, Yildiz, Yilmaz, Yucel Yilmaz, Didem, Pektas, Emine, Tokatli, Aysegul, ozgul, R. Koksal, Sivri, H. Serap, Dursun, Ali

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Phenylketonuria: A Scoring System for Brain Magnetic Resonance Imaging von Bako, Derya, Çıkı, Kısmet

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An Infant With Congenital Leukemia Cutis and AML-M5 With MLL Gene Rearrangement von Bayhan, Turan, Çiki, Kismet, Tavil, Betül, Gümrük, Fatma, Çetin, Mualla, Ünal, Şule

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COVID-19 in inherited metabolic disorders: Clinical features and risk factors for disease severity von Kahraman, Ayca Burcu, Yıldız, Yılmaz, Çıkı, Kısmet, Erdal, Izzet, Akar, Halil Tuna, Dursun, Ali, Tokatlı, Ayşegül, Sivri, Serap

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Evaluation of sleep‐disordered breathing and its relationship with respiratory parameters in children with mucopolysaccharidosis Type IVA and VI von Ademhan Tural, Dilber, Emiralioglu, Nagehan, Dogru, Deniz, Ozsezen, Beste, Ipek, Omer Faruk, Sunman, Birce, Nayir Buyuksahin, Halime, Guzelkas, Ismail, Ciki, Kismet, Kilic, Kubra, Vardar Yagli, Naciye, Yalcin, Ebru, Kiper, Nural, Sivri, Serap, Ozcelik, Ugur

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Predictors of eventual requirement of phenylalanine-restricted diet in young infants with phenylalanine hydroxylase deficiency initially managed with sapropterin monotherapy von Çıkı, Kısmet, Yıldız, Yılmaz, Kahraman, Ayça Burcu, Özgül, R. Köksal, Coşkun, Turgay, Dursun, Ali, Tokatlı, Ayşegül, Sivri, Serap

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DNACJ12 deficiency in patients with unexplained hyperphenylalaninemia: two new patients and a novel variant von Çıkı, Kısmet, Yıldız, Yılmaz, Yücel Yılmaz, Didem, Pektaş, Emine, Tokatlı, Ayşegül, Özgül, R. Köksal, Sivri, H. Serap, Dursun, Ali

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Cardiomyopathy in patients with type 1 tyrosinemia, and the effect of nitisinone treatment on cardiomyopathy von Bilginer Gürbüz,Berrak, Aykan,Hayrettin Hakan, Çıkı,Kısmet, Karagöz,Tevfik, Sivri,Hatice Serap, Dursun,Ali, Tokatlı,Ayşegül, Coşkun,Turgay

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A fatal Clostridium perfringens infection with hemolysis after chemotherapy in an adolescent von Kukul, Musa G, Ciki, Kısmet, Karadag-Oncel, Eda, Cengiz, Ali B, Kuskonmaz, Baris, Tavil, Betul, Kesici, Selman

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Pulmonary complications following hematopoietic stem cell transplantation in children von Çıkı, Kısmet, Doğru, Deniz, Kuşkonmaz, Barış, Emiralioğlu, Nagehan, Yalçın, Ebru, Özçelik, Uğur, Uçkan-Çetinkaya, Duygu, Kiper, Nural

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A rare cause of acute abdominal pain in a patient with Primary ciliary dyskinesia with situs inversus totalis von Ciki, Kismet, Turer, Ozlem Boybeyi, Hizal, Mina, Tugcu, Gokcen Dilsa, Emiralioglu, Nagehan, Yalcin, Ebru, Ersoz, Deniz Dogru, Kiper, Nural, Ozcelik, Ugur

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Correction to: DNAJC12 deficiency in patients with unexplained hyperphenylalaninemia: two new patients and a novel variant von Çıkı, Kısmet, Yıldız, Yılmaz, Yücel Yılmaz, Didem, Pektaş, Emine, Tokatlı, Ayşegül, Özgül, R. Köksal, Sivri, H. Serap, Dursun, Ali

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Efficacy of Tele-CO-OP in Children With Organic Acidemia: A Pilot Randomized Controlled Trial von Dursun, Esra Leman, Bumin, Gonca, Çıkı, Kısmet, Sivri, Serap

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Infección mortal por Clostridium perfringens con hemólisis tras quimioterapia en un adolescente von Kukul, Musa G, Ciki, Kismet, Karadag-Oncel, Eda, Cengiz, Ali B, Kuskonmaz, Baris, Tavil, Betul, Kesici, Selman

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An Infant With Congenital Leukemia Cutis and AML-M5 With MLL Gene Rearrangement von Bayhan, Turan, Çiki, Kismet, Tavil, Betül, Gümrük, Fatma, Çetin, Mualla, Ünal, Şule

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Comprehensive analysis of genotypic and phenotypic characteristics of biotinidase deficiency patients in the eastern region of Türkiye von Çıkı, Kısmet, Alavanda, Ceren, Ceylan, Emine İpek, Tanyalçın, Tijen, Kılavuz, Sebile

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