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Journal of Inherited Metabolic Disease|July 17, 1999
4-Aminobutyrate aminotransferase (GABA-transaminase) deficiencyL K Medina-Kauwe, A J Tobin, L De Meirleir, et al.Journal of Inherited Metabolic Disease|July 17, 1999
Neurochemistry and defects of biogenic amine neurotransmitter metabolismK HylandJournal of Inherited Metabolic Disease|July 17, 1999
Genomics, mutations and the Internet: the naming and use of partsC R Scriver, P M NowackiJournal of Inherited Metabolic Disease|July 17, 1999
The spectrum of mutations of the aspartoacylase gene in Canavan disease in non-Jewish patientsO N Elpeleg, A ShaagJournal of Inherited Metabolic Disease|February 22, 2000
Brain phenylalanine concentration in the management of adults with phenylketonuriaR A Moats, R Koch, K Moseley, et al.Journal of Inherited Metabolic Disease|February 22, 2000
Treatment of late-onset nonketotic hyperglycinaemia: effectiveness of imipramine and benzoateE J Wiltshire, N K Poplawski, J R Harrison, et al.Journal of Inherited Metabolic Disease|June 23, 2000
Disorders related to mitochondrial membranes: pathology of the respiratory chain and neurodegenerationS Di DonatoJournal of Inherited Metabolic Disease|July 10, 1999
Liver transplantation for citrullinaemia improves intellectual functionJ M Fletcher, R Couper, D Moore, et al.Journal of Inherited Metabolic Disease|July 10, 1999
3-Methylglutaconic aciduria and hypermethioninaemia in a child with clinical and neuroradiological findings of Leigh diseaseM Di Rocco, U Caruso, I Moroni, et al.Journal of Inherited Metabolic Disease|July 10, 1999
Long-term follow-up following bone marrow transplantation for Hunter diseaseA Vellodi, E Young, A Cooper, et al.Pageof 429