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Ivo Barić

University of Zagreb

190

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3151

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Early initiation of ambroxol treatment diminishes neurological manifestations of type 3 Gaucher disease: A long-term outcome of two siblings.

2021 European Journal of Paediatric Neurology
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253 Refractory cyclic vomiting syndrome in a child with Chiari malformation type II

2021 Archives of Disease in Childhood
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Advanced skeletal muscle imaging in S-Adenosylhomocysteine Hydrolase Deficiency: A case series

2021
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106 Diversity of clinical phenotype of patients with pyruvate dehydrogenase deficiency due to PDHA1 gene mutations

2021 Archives of Disease in Childhood
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Hereditary fructose intolerance – two case reports and literature review

2021 Paediatria Croatica
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Current Status of Newborn Screening in Southeastern Europe

2021 Frontiers in Pediatrics
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Inborn Errors of Metabolism Associated With Autism Spectrum Disorders: Approaches to Intervention

2021 Frontiers in Neuroscience
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NBAS Variants Are Associated with Quantitative and Qualitative NK and B Cell Deficiency.

2021 Journal of Clinical Immunology
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107 Early onset liver failure due to mitochondrial DNA depletion: clinical course of four patients

2021 Archives of Disease in Childhood
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104 Hypoketotic hypoglycemia and hyperammonemia as presenting features of early onset multiple acyl-CoA dehydrogenase deficiency

2021 Archives of Disease in Childhood
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