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Molecular Genetics and Metabolism|July 22, 2019
Long-term safety and efficacy of glycerol phenylbutyrate for the management of urea cycle disorder patientsGeorge A Diaz, Andreas Schulze, Nicola Longo, et al.Journal of Neurogenetics|April 1, 1984
3-Hydroxy-3-methylglutaric aciduriaC L Greene, H M Cann, B H Robinson, et al.European Journal of Pediatrics|August 1, 1993
Multiple respiratory chain abnormalities associated with hypertrophic cardiomyopathy and 3-methylglutaconic aciduriaH Ibel, W Endres, H B Hadorn, et al.Pediatric Research|August 1, 1993
Decreased plasma ubiquinone-10 concentration in patients with mevalonate kinase deficiencyC Hübner, G F Hoffmann, C Charpentier, et al.JIMD Reports|February 23, 2013
Efficacy of vigabatrin intervention in a mild phenotypic expression of succinic semialdehyde dehydrogenase deficiencyM Casarano, M G Alessandrì, G S Salomons, et al.Journal of Neurogenetics|April 1, 1985
Properties of succinic semialdehyde dehydrogenase in cultured human lymphoblastsK M Gibson, L Sweetman, I Jansen, 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.Cancer Research|October 23, 1997
R-flurbiprofen chemoprevention and treatment of intestinal adenomas in the APC(Min)/+ mouse model: implications for prophylaxis and treatment of colon cancerW J Wechter, D Kantoci, E D Murray, et al.Journal of Inherited Metabolic Disease|June 2, 2009
Visual evoked potentials in succinate semialdehyde dehydrogenase (SSADH) deficiencyG Di Rosa, P Malaspina, P Blasi, et al.Journal of Inherited Metabolic Disease|January 31, 2003
Prenatal diagnosis of succinate semialdehyde dehydrogenase deficiency in non-identical twinsI A Aligianis, P A Farndon, R G F Gray, et al.Pageof 25