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American Journal of Human Genetics|May 1, 1983
The prognosis of hyperlysinemia: an interim reportJ Dancis, J Hutzler, M G Ampola, et al.American Journal of Human Genetics|November 1, 1990
Splicing defect at the ornithine aminotransferase (OAT) locus in gyrate atrophyA I McClatchey, D L Kaufman, E L Berson, et al.Prenatal Diagnosis|July 1, 1986
Prenatal diagnosis of non-ketotic hyperglycinemiaD A Applegarth, H L Levy, V E Shih, et al.Archives of Neurology|September 1, 1992
An antispasticity effect of threonine in multiple sclerosisS L Hauser, T H Doolittle, M Lopez-Bresnahan, et al.Transplantation|October 31, 2001
Vascular endothelial function in cyclosporine and tacrolimus treated renal transplant recipientsC A Ovuworie, E R Fox, C M Chow, et al.The New England Journal of Medicine|November 10, 1977
Sulfite oxidase deficiency. Biochemical and clinical investigations of a hereditary metabolic disorder in sulfur metabolismV E Shih, I F Abroms, J L Johnson, et al.Neurology|November 1, 1980
Glutaric acidemia: a metabolic disorder causing progressive choreoathetosisR L Leibel, V E Shih, S I Goodman, et al.Stroke|December 6, 2003
Inflammation, homocysteine, and vitamin B6 status after ischemic strokeP J Kelly, J P Kistler, V E Shih, et al.American Journal of Human Genetics|July 1, 1995
A missense mutation (I278T) in the cystathionine beta-synthase gene prevalent in pyridoxine-responsive homocystinuria and associated with mild clinical phenotypeV E Shih, J M Fringer, R Mandell, et al.Journal of Inherited Metabolic Disease|September 10, 2005
Ornithine aminotransferase deficiency: diagnostic difficulties in neonatal presentationM A Cleary, L Dorland, T J de Koning, et al.Pageof 10