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Journal of Inherited Metabolic Disease|August 7, 2010
Pulmonary hemorrhage in type 3 Gaucher disease: a case reportAshok Vellodi, Michael Ashworth, Niamh Finnegan, et al.Journal of Inherited Metabolic Disease|June 26, 2010
Present and future of antisense therapy for splicing modulation in inherited metabolic diseaseBelen Pérez, Laura Rodríguez-Pascau, Luisa Vilageliu, et al.Journal of Inherited Metabolic Disease|September 11, 2010
Long-term follow-up results in enzyme replacement therapy for Pompe disease: a case reportMonica Del Rizzo, Marina Fanin, Alessia Cerutti, et al.Journal of Inherited Metabolic Disease|September 11, 2010
Current issues regarding treatment of mitochondrial fatty acid oxidation disordersUte Spiekerkoetter, Jean Bastin, Melanie Gillingham, et al.Journal of Inherited Metabolic Disease|January 1, 1990
The inborn errors of peroxisomal beta-oxidation: a reviewR J Wanders, C W van Roermund, R B Schutgens, et al.Journal of Inherited Metabolic Disease|November 25, 2010
Enzymology of the branched-chain amino acid oxidation disorders: the valine pathwayRonald J A Wanders, Marinus Duran, Ference J LoupattyJournal of Inherited Metabolic Disease|November 20, 2010
Novel ETF dehydrogenase mutations in a patient with mild glutaric aciduria type II and complex II-III deficiency in liver and muscleLynne A Wolfe, Miao He, Jerry Vockley, et al.Journal of Inherited Metabolic Disease|February 3, 2011
Sub-pleural bullous changes in two adults with Mucopolysaccharidosis type I (Hurler-Scheie)Michel C Tchan, Nicole Graf, David O SillenceJournal of Inherited Metabolic Disease|February 4, 2011
Features and outcome of galactokinase deficiency in children diagnosed by newborn screeningJulia B Hennermann, Peter Schadewaldt, Barbara Vetter, et al.Journal of Inherited Metabolic Disease|February 4, 2011
Advances and challenges in the treatment of branched-chain amino/keto acid metabolic defectsIna Knerr, Natalie Weinhold, Jerry Vockley, et al.Pageof 429