PROPIONIC ACIDURIA IN A 5-MONTH-OLD CHILD by L. D. Fominykh, G. V. Solovyeva, M. L. Vyaznikova, N. G. Muratova, T. E. Serebrenikova, E. A. Kostyuchek

Subjects: “…hereditary metabolic diseases…”
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Clinical Course of Methylmalonic Aciduria in Siblings: Two Clinical Cases by Olga V. Bugun, Galina P. Bogonosova, Tatyana A. Astakhova, Tatyana A. Bairova, Natalya N. Martynovich, Darya M. Barycova, Tatyana Y. Belkova, Yuliya S. Livadarova, Nanalya I. Sysoeva

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Features of clinical manifestations and treatment of individual nosological forms of hereditary metabolic diseases by L. V. Goroshko, E. G. Bakulina

Subjects: “…hereditary metabolic diseases…”
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Report on advances for pediatricians in 2018: allergy, cardiology, critical care, endocrinology, hereditary metabolic diseases, gastroenterology, infectious diseases, neonatology,... by Carlo Caffarelli, Francesca Santamaria, Carla Mastrorilli, Angelica Santoro, Brunella Iovane, Maddalena Petraroli, Valeria Gaeta, Rosita Di Pinto, Melissa Borrelli, Sergio Bernasconi, Giovanni Corsello

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ORNITHINE TRANSCARBAMYLASE DEFICIENCY – THE REAL CAUSE OF “FAMILY CURSE”. A CASE REPORT by Zh. Sh. Bagomedova, A. S. Kotov, M. N. Borisova, M. V. Panteleeva, N. V. Zhurkova, A. A. Byome, Yu. Yu. Kotalevskaya, O. S. Mironova, I. V. Razheva

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Research activity and capability in the European reference network MetabERN by Jean-Michel Heard, Cinzia Bellettato, Corine van Lingen, Maurizio Scarpa, the MetabERN collaboration group

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Clinical and Laboratory Markers of Hereditary Metabolic Diseases in Children of the First Half of Life by N. N. Martynovich, N. E. Globenko, S. N. Kuznetsova

Subjects: “…hereditary metabolic diseases…”
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Availability, accessibility and delivery to patients of the 28 orphan medicines approved by the European Medicine Agency for hereditary metabolic diseases in the MetabERN network by Jean-Michel Heard, Charlotte Vrinten, Michael Schlander, Cinzia Maria Bellettato, Corine van Lingen, Maurizio Scarpa, the MetabERN collaboration group

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Specific characteristics of dynamic monitoring of patients diagnosed with classical phenylketonuria during pregnancy by E. A. Shestopalova

Subjects: “…hereditary metabolic diseases…”
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DYSTONIA IN CHILDREN (A LECTURE) by M. Yu. Bobylova, V. S. Kakaulina, E. S. Ilyina, I. V. Nekrasova, N. L. Pechatnikova, S. V. Mikhailova, M. B. Mironov, K. Yu. Mukhin

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ORGANIZATION OF PSYCHOLOGY AND PEDAGOGICAL CARE IN CHILDREN WITH SEVERE CHRONIC HEREDITARY METABOLIC DISEASES REHABILITATION (AT THE MODEL OF MUCOPOLYSACCHARIDOSIS) by S. B. Lazurenko, L. S. Namazova-Baranova

Subjects: “…children with hereditary metabolic diseases health…”
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Case report: Rhabdomyolysis in children in acute and chronic disease—a challenging condition in pediatric emergency medicine by N. Mand, C. Donath, A. Leonhardt, S. Weber, M. Kömhoff

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Current Status and Prospects of Screening for Newborn Hereditary Metaboolic Disease by GU Xuefan, HAN Lianshu, YU Yongguo

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