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JIMD Reports|December 16, 2014
Neurodevelopmental profiles of children with glutaric aciduria type I diagnosed by newborn screening: a follow-up case seriesAmy Brown, Louise Crowe, Miriam H Beauchamp, et al.JIMD Reports|October 3, 2015
Intracranial Pressure Monitoring Demonstrates that Cerebral Edema Is Not Correlated to Hyperammonemia in a Child with Ornithine Transcarbamylase DeficiencyJulie Chantreuil, Géraldine Favrais, Nadine Fakhri, et al.JIMD Reports|October 11, 2015
Electroclinical Features of Early-Onset Epileptic Encephalopathies in Congenital Disorders of Glycosylation (CDGs)Agata Fiumara, Rita Barone, Giuliana Del Campo, et al.JIMD Reports|October 18, 2015
Lethal Neonatal Progression of Fetal Cardiomegaly Associated to ACAD9 DeficiencyJennifer Lagoutte-Renosi, Isabelle Ségalas-Milazzo, Marie Crahes, et al.JIMD Reports|September 28, 2015
Hyperprolinemia in Type 2 Glutaric Aciduria and MADD-Like ProfilesClément Pontoizeau, Florence Habarou, Anaïs Brassier, et al.JIMD Reports|September 27, 2014
Early Umbilical Cord Blood-Derived Stem Cell Transplantation Does Not Prevent Neurological Deterioration in Mucopolysaccharidosis Type IIILindsey Welling, Jan Pieter Marchal, Peter van Hasselt, et al.JIMD Reports|September 13, 2014
Hypertrophic cardiomyopathy in pompe disease is not limited to the classic infantile-onset phenotypeDong-Hwan Lee, Wen-Juan Qiu, Jeongho Lee, et al.JIMD Reports|July 21, 2014
Perioperative medullary complications in spinal and extra-spinal surgery in mucopolysaccharidosis: a case series of three patientsN Pauchard, C Garin, J L Jouve, et al.JIMD Reports|July 12, 2014
Birth Prevalence of Fatty Acid β-Oxidation Disorders in IberiaHugo Rocha, Daisy Castiñeiras, Carmen Delgado, et al.JIMD Reports|July 12, 2014
NMR-Based Screening for Inborn Errors of Metabolism: Initial Results from a Study on Turkish NeonatesSitke Aygen, Ulrich Dürr, Peter Hegele, et al.Pageof 127