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Journal of Inherited Metabolic Disease|January 7, 2004
Efficacy of multidisciplinary approach in the treatment of two cases of nonclassical infantile glycogenosis type IIB Bembi, G Ciana, C Martini, et al.Journal of Inherited Metabolic Disease|January 7, 2004
Rhabdomyolysis in glutaric aciduria type IS L Chow, C Rohan, A A M MorrisJournal of Inherited Metabolic Disease|January 24, 2004
Homocystinuria due to cystathionine beta-synthase deficiency: novel biochemical findings and treatment efficacyM Orendác, J Zeman, S P Stabler, et al.Journal of Inherited Metabolic Disease|November 8, 2003
A description of an HPLC assay of coproporphyrinogen III oxidase activity in mononuclear cellsU Gross, R Gerlach, A Kühnel, et al.Journal of Inherited Metabolic Disease|November 8, 2003
Stereoselective analysis of 2-hydroxysebacic acid in urine of patients with Zellweger syndrome and of premature infants fed with medium-chain triglyceridesA Muth, A Mosandl, R J A Wanders, et al.Journal of Inherited Metabolic Disease|November 8, 2003
Exercise intolerance, muscle pain and lactic acidaemia associated with a 7497G>A mutation in the tRNASer(UCN) geneO Grafakou, F A Hol, K Otfried Schwab, et al.Journal of Inherited Metabolic Disease|June 11, 2004
Mitochondrial disorders: prevalence, myths and advancesD R ThorburnJournal of Inherited Metabolic Disease|June 11, 2004
Hepatocyte transplantation for inborn errors of metabolismA B BurlinaJournal of Inherited Metabolic Disease|August 11, 2004
The role of oxidative damage in the neuropathology of organic acidurias: insights from animal studiesM Wajner, A Latini, A T S Wyse, et al.Journal of Inherited Metabolic Disease|August 11, 2004
OCTN2 mutation (R254X) found in Saudi Arabian kindred: recurrent mutation or ancient founder mutation?A-M Lamhonwah, R Onizuka, S E Olpin, et al.Pageof 429