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Current Opinion in Neurology and Neurosurgery|June 1, 1992
Neurological diseases in disorders of organic acidsD L Marsden, W L NyhanJournal of Inherited Metabolic Disease|May 20, 2005
Normal acylcarnitine levels during confirmation of abnormal newborn screening in long-chain fatty acid oxidation defectsM F Browning, C Larson, A Strauss, et al.Birth Defects Original Article Series|January 1, 1989
Metabolic correlates of learning disabilityW L Nyhan, B B Wulfeck, P Tallal, et al.Stroke Research and Treatment|February 17, 2015
Protocol variations and six-minute walk test performance in stroke survivors: a systematic review with meta-analysisA Dunn, D L Marsden, E Nugent, et al.Pediatric Pathology|March 1, 1994
Histopathological findings in a male with late-onset ornithine transcarbamylase deficiencyS Capistrano-Estrada, D L Marsden, W L Nyhan, et al.Journal of Child Neurology|January 1, 1995
Acute basal ganglia infarction in propionic acidemiaR H Haas, D L Marsden, S Capistrano-Estrada, et al.The Journal of Clinical Endocrinology and Metabolism|September 1, 1997
Diabetes and mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS): radiolabeled polymerase chain reaction is necessary for accurate detection of low percentages of mutationM L Smith, X Y Hua, D L Marsden, et al.Molecular Genetics and Metabolism|September 4, 2016
Triheptanoin treatment in patients with pediatric cardiomyopathy associated with long chain-fatty acid oxidation disordersJ Vockley, J Charrow, J Ganesh, et al.Molecular Genetics and Metabolism|February 13, 2017
UX007 for the treatment of long chain-fatty acid oxidation disorders: Safety and efficacy in children and adults following 24weeks of treatmentJ Vockley, B Burton, G T Berry, et al.Pageof 1