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Journal of Inherited Metabolic Disease|January 1, 1984
Paired comparisons between early treated PKU children and their matched sibling controls on intelligence and school achievement test results at eight years of ageR Koch, C Azen, E G Friedman, et al.Journal of Inherited Metabolic Disease|January 1, 1984
The management and long term outcome of organic acidaemiasJ V Leonard, P Daish, E R Naughten, et al.Journal of Inherited Metabolic Disease|January 1, 1984
Prenatal diagnosis of the organic aciduriasL SweetmanJournal of Inherited Metabolic Disease|January 1, 1984
Symptoms and signs in organic aciduriasN J BrandtJournal of Inherited Metabolic Disease|January 1, 1984
Animal models for dicarboxylic aciduriaH S Sherratt, R K VeitchJournal of Inherited Metabolic Disease|October 27, 2009
RFT1-CDG: deafness as a novel feature of congenital disorders of glycosylationJ Jaeken, W Vleugels, L Régal, et al.Journal of Inherited Metabolic Disease|January 1, 1983
Glycogen storage diseases in animals and their potential value as models of human diseaseH C WalvoortJournal of Inherited Metabolic Disease|January 1, 1983
Kinetic analysis of argininosuccinate synthetase in a variant form of citrullinaemiaI Akaboshi, F Endo, I Matsuda, et al.Journal of Inherited Metabolic Disease|January 1, 1983
The iduronate sulphatase activities of cells and tissue fluids from patients with Hunter syndrome and normal controlsM F DeanJournal of Inherited Metabolic Disease|January 1, 1983
Chemical studies on postmortem tissues from an infant with a sphingomyelin storage disorderS F Donaghey, D N Raine, J E CrossleyPageof 429