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Journal of Inherited Metabolic Disease|February 19, 2004
Reversion of hypertrophic cardiomyopathy in a patient with deficiency of the mitochondrial copper binding protein Sco2: is there a potential effect of copper?P Freisinger, R Horvath, C Macmillan, et al.Journal of Inherited Metabolic Disease|May 26, 2004
Executive function impairment in early-treated PKU subjects with normal mental developmentV Leuzzi, M Pansini, E Sechi, et al.Journal of Inherited Metabolic Disease|April 7, 2004
Energy expenditure in patients with propionic and methylmalonic acidaemiasC C van Hagen, E Carbasius Weber, Th A M van den Hurk, et al.Journal of Inherited Metabolic Disease|May 4, 2005
Molecular mechanism of dominant expression in 3-methylcrotonyl-CoA carboxylase deficiencyM R BaumgartnerJournal of Inherited Metabolic Disease|May 4, 2005
Oligodendrocytes and stem cell transplantation: their potential in the treatment of leukoencephalopathiesI D DuncanJournal of Inherited Metabolic Disease|May 4, 2005
Methylmalonic and propionic acidaemias: management and outcomeH Ogier de Baulny, J F Benoist, O Rigal, et al.Journal of Inherited Metabolic Disease|May 7, 2005
L-carnitine and exercise tolerance in medium-chain acyl-coenzyme A dehydrogenase (MCAD) deficiency: a pilot studyP J Lee, E L Harrison, M G Jones, et al.Journal of Inherited Metabolic Disease|May 7, 2005
Selective antibody immune deficiency in a patient with Smith-Lemli-Opitz syndromeD Babovic-Vuksanovic, R M Jacobson, N M Lindor, et al.Journal of Inherited Metabolic Disease|May 7, 2005
N-carbamylglutamate protects patients with decompensated propionic aciduria from hyperammonaemiaB Gebhardt, S Dittrich, S Parbel, et al.Pageof 429