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V E Shih

Showing results (61-70 of 112) with videos related to

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Biochemical and Biophysical Research Communications|February 19, 2000
Cloning and characterization of a putative human d-2-hydroxyacid dehydrogenase in chromosome 9qT Huang, W Yang, A C Pereira, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 8, 1981
Variation in argininosuccinate synthetase activity in amniotic fluid cell cultures: implications for prenatal diagnosis of citrullinemiaL B Jacoby, V E Shih, C Struckmeyer, et al.
DNA (Mary Ann Liebert, Inc.)|December 1, 1986
Investigation of gyrate atrophy using a cDNA clone for human ornithine aminotransferaseV Ramesh, M M Shaffer, J M Allaire, et al.
American Journal of Human Genetics|May 1, 1972
A microassay for argininosuccinase in cultured cellsL B Jacoby, J W Littlefield, A Milunsky, et al.
The New England Journal of Medicine|October 18, 1984
Benign methylmalonic aciduriaF D Ledley, H L Levy, V E Shih, et al.
Genomics|October 1, 1992
Three novel mutations of the ornithine aminotransferase (OAT) gene in gyrate atrophyJ K Park, B J Herron, J J O'Donnell, et al.
Human Mutation|January 1, 1992
A 15-bp deletion in exon 5 of the ornithine aminotransferase (OAT) locus associated with gyrate atrophyJ K Park, J J O'Donnell, V E Shih, et al.
Clinical Genetics|September 1, 1984
Occurrences of methylmalonic aciduria and Hartnup disorder in the same familyV E Shih, J T Coulombe, S K Wadman, et al.
Pediatric Neurology|April 13, 2001
Carbamyl phosphate synthetase 1 deficiency: a destructive encephalopathyM Takeoka, T B Soman, V E Shih, et al.
Journal of Inherited Metabolic Disease|January 27, 2005
Successful long-term treatment of hepatic carnitine palmitoyltransferase I deficiency and a novel mutationJ M Stoler, M A Sabry, C Hanley, et al.
Pageof 12

Showing results (61-70 of 112) with videos related to

Sort By:
Pageof 12
Biochemical and Biophysical Research Communications|February 19, 2000
Cloning and characterization of a putative human d-2-hydroxyacid dehydrogenase in chromosome 9qT Huang, W Yang, A C Pereira, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 8, 1981
Variation in argininosuccinate synthetase activity in amniotic fluid cell cultures: implications for prenatal diagnosis of citrullinemiaL B Jacoby, V E Shih, C Struckmeyer, et al.
DNA (Mary Ann Liebert, Inc.)|December 1, 1986
Investigation of gyrate atrophy using a cDNA clone for human ornithine aminotransferaseV Ramesh, M M Shaffer, J M Allaire, et al.
American Journal of Human Genetics|May 1, 1972
A microassay for argininosuccinase in cultured cellsL B Jacoby, J W Littlefield, A Milunsky, et al.
The New England Journal of Medicine|October 18, 1984
Benign methylmalonic aciduriaF D Ledley, H L Levy, V E Shih, et al.
Genomics|October 1, 1992
Three novel mutations of the ornithine aminotransferase (OAT) gene in gyrate atrophyJ K Park, B J Herron, J J O'Donnell, et al.
Human Mutation|January 1, 1992
A 15-bp deletion in exon 5 of the ornithine aminotransferase (OAT) locus associated with gyrate atrophyJ K Park, J J O'Donnell, V E Shih, et al.
Clinical Genetics|September 1, 1984
Occurrences of methylmalonic aciduria and Hartnup disorder in the same familyV E Shih, J T Coulombe, S K Wadman, et al.
Pediatric Neurology|April 13, 2001
Carbamyl phosphate synthetase 1 deficiency: a destructive encephalopathyM Takeoka, T B Soman, V E Shih, et al.
Journal of Inherited Metabolic Disease|January 27, 2005
Successful long-term treatment of hepatic carnitine palmitoyltransferase I deficiency and a novel mutationJ M Stoler, M A Sabry, C Hanley, et al.
Pageof 12