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V E Shih

Showing results (101-110 of 112) with videos related to

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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.
The New England Journal of Medicine|August 19, 1971
Persistent mild hyperphenylalaninemia in the untreated state. A prospective studyH L Levy, V E Shih, V Karolkewicz, 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.
The New England Journal of Medicine|January 14, 1982
Prenatal diagnosis of nonketotic hyperglycinemiaJ M García-Castro, C M Isales-Forsythe, H L Levy, 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.
Clinical Chemistry|October 24, 2001
Tandem mass spectrometric analysis for amino, organic, and fatty acid disorders in newborn dried blood spots: a two-year summary from the New England Newborn Screening ProgramT H Zytkovicz, E F Fitzgerald, D Marsden, et al.
Journal of Inherited Metabolic Disease|March 18, 2003
Newborn screening compared to clinical identification of biochemical genetic disordersS E Waisbren, C Y Read, M Ampola, et al.
Molecular Genetics and Metabolism|June 23, 1998
Molecular analysis and prenatal diagnosis of human fumarase deficiencyE M Coughlin, E Christensen, P L Kunz, et al.
Pageof 12

Showing results (101-110 of 112) with videos related to

Sort By:
Pageof 12
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.
The New England Journal of Medicine|August 19, 1971
Persistent mild hyperphenylalaninemia in the untreated state. A prospective studyH L Levy, V E Shih, V Karolkewicz, 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.
The New England Journal of Medicine|January 14, 1982
Prenatal diagnosis of nonketotic hyperglycinemiaJ M García-Castro, C M Isales-Forsythe, H L Levy, 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.
Clinical Chemistry|October 24, 2001
Tandem mass spectrometric analysis for amino, organic, and fatty acid disorders in newborn dried blood spots: a two-year summary from the New England Newborn Screening ProgramT H Zytkovicz, E F Fitzgerald, D Marsden, et al.
Journal of Inherited Metabolic Disease|March 18, 2003
Newborn screening compared to clinical identification of biochemical genetic disordersS E Waisbren, C Y Read, M Ampola, et al.
Molecular Genetics and Metabolism|June 23, 1998
Molecular analysis and prenatal diagnosis of human fumarase deficiencyE M Coughlin, E Christensen, P L Kunz, et al.
Pageof 12