“Double Hit” Homozygous Mutations for Two Different Rare Inborn Errors of Metabolism: A Burden for Countries with High Prevalences of Consangineous Marriages by Asburçe Olgaç, Leyla Tümer, Serdar Ceylaner, Gürsel Biberoğlu, Alev Hasanoğlu

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Lysinuric protein intolerance: an overlooked diagnosis by Asburce Olgac, Idil Yenicesu, Rıza Köksal Ozgul, Gürsel Biberoğlu, Leyla Tümer

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Clinical and event-based outcomes of patients with mucopolysaccharidosis VI receiving enzyme replacement therapy in Turkey: a case series by Aslı İnci, İlyas Okur, Leyla Tümer, Gürsel Biberoğlu, Murat Öktem, Fatih Ezgü

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The levels of asymmetric dimethylarginine, homocysteine and carotid intima-media thickness in hypercholesterolemic children by Alev Hasanoğlu, Ilyas Okur, Ayşe Ceyda Oren, Gürsel Biberoğlu, Suna Oktar, Fatma Tuba Eminoğlu, Leyla Tümer

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Neonatal multiple sulfatase deficiency with a novel mutation and review of the literature by Banu Güzel Nur, Ercan Mıhçı, Stefano Pepe, Gürsel Biberoğlu, Fatih Süheyl Ezgü, Andrea Ballabio, Osman Öztekin, Oğuz Dursun

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