Alpha-mannosidosis and mutational analysis in a Turkish patient by Akgün Olmez, Oivind Nilssen, Turgay Coşkun, Helle Klenow

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Assessment of tetrahydrobiopterin responsiveness in Turkish hyperphenylalaninemic patients by Sükran Yildirim, Ayşegül Tokatli, Engin Yilmaz, Turgay Coşkun

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Fanconi-Bickel syndrome in three Turkish patients with different homozygous mutations by Inci Nur Saltik-Temizel, Turgay Coşkun, Aysel Yüce, Nurten Koçak

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Neurophysiologic features in glutaric aciduria type I by Dilek Yalnizoğlu, Neriman Sari, Güzide Turanli, Turgay Coşkun, Meral Topçu

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Nutritional status of children with cancer and its effects on survival by Nilgün Yariş, Canan Akyüz, Turgay Coşkun, Tezer Kutluk, Münevver Büyükpamukçu

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Acetaminophen-induced hepatotoxicity in a glutathione synthetase-deficient patient by Ayşegül Tokatli, H Serap Kalkanoğlu-Sivri, Aysel Yüce, Turgay Coşkun

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Gyrate atrophy of the choroid and retina: a case report by Nesrin Büyüktortop, Mehmet Numan Alp, Serap Sivri, Turgay Coşkun, Gülcan Kural

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Late-diagnosed phenylketonuria in an eight-year-old boy with dyslexia and attention-deficit hyperactivity disorder by Yılmaz Yıldız, Ali Dursun, Ayşegül Tokatlı, Turgay Coşkun, Hatice Serap Sivri

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Maternal and environmental determinants of breast-milk mercury concentrations by S Songül Yalçin, Kadriye Yurdakök, Suzan Yalçin, Defne Engür-Karasimav, Turgay Coşkun

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Vitamin D receptor gene polymorphisms in Turkish children with vitamin D deficient rickets by Gamze Bora, Behzat Ozkan, Didem Dayangaç-Erden, Hayat Erdem-Yurter, Turgay Coşkun

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Two cases of Vici syndrome presenting with corpus callosum agenesis, albinism, and severe developmental delay by Mina Hızal, Batuhan Yeke, Yılmaz Yıldız, Ali Öztürk, Berrak Bilginer Gürbüz, Turgay Coşkun

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Erratum to `Recommendations on phenylketonuria in Turkey` [Turk J Pediatr 2022; 64: 413-434] by Turgay Coşkun, Mahmut Çoker, Neslihan Önenli Mungan, Hülya Gökmen Özel, H Serap Sivri

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A case of fucosidosis type II: diagnosed with dysmorphological and radiological findings by Esra Kılıç, Mustafa Kılıç, G Eda Ütine, Serap Sivri, Turgay Coskun, Yasemin Alanay

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Home visits in phenylketonuria: a 12-month longitudinal study by Hülya Gökmen-Ozel, Zehra Büyüktuncer, Gülden Köksal, H Serap Kalkanoğlu-Sivri, Turgay Coşkun

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Recommendations on phenylketonuria in Turkey by Turgay Coşkun, Mahmut Çoker, Neslihan Önenli Mungan, Hülya Gökmen Özel, H Serap Sivri

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When do we need to perform a diagnostic lumbar puncture for neurometabolic diseases? Positive yield and retrospective analysis from a tertiary center by Göknur Haliloğlu, Emine Vezir, Leyla Baydar, Saniye Onol, Serap Sivri, Turgay Coşkun, Meral Topçu

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Autism spectrum disorder in patients with inherited metabolic disorders-a large sample from a tertiary center by Tuba Çelen Yoldaş, Berrak Bilginer Gürbüz, Halil Tuna Akar, Elif Nursel Özmert, Turgay Coşkun

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Conventional and advanced MR imaging in infantile Refsum disease by Mustafa Kılıç, Kader Karlı-Oğuz, Göknur Haliloğlu, Meral Topçu, Ronald James Wanders, Turgay Coşkun

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Two new cases with Pearson syndrome and review of Hacettepe experience by Rezan Topaloğlu, Anne S Lebre, Erkan Demirkaya, Bariş Kuşkonmaz, Turgay Coşkun, Diclehan Orhan, Aytemiz Gürgey, Fatma Gümrük

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Serum alpha-fetoprotein levels in neonatal cholestasis by Hülya Demir, Gülin Hızal, Nuray Uslu Kızılkan, Figen Gürakan, Beril Talim, Turgay Coşkun, Gülsev Kale, Aysel Yüce

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