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The Journal of Clinical Investigation|March 1, 1989
Molybdenum cofactor biosynthesis in humans. Identification of two complementation groups of cofactor-deficient patients and preliminary characterization of a diffusible molybdopterin precursorJ L Johnson, M M Wuebbens, R Mandell, et al.
Birth Defects Original Article Series|January 1, 1982
A two year trial of low protein, low arginine diets or vitamin B6 for patients with gyrate atrophyE L Berson, A H Hanson, B Rosner, et al.
American Journal of Human Genetics|March 1, 1978
Ornithine ketoacid transaminase deficiency in gyrate atrophy of the choroid and retinaV E Shih, E L Berson, R Mandell, et al.
Annals of Neurology|February 1, 1982
D-lactic acidosis simulating a hypothalamic syndrome after bowel bypassD B Carr, V E Shih, J M Richter, et al.
Archives of Internal Medicine|June 1, 1975
Hereditary pancreatitis. Nonspecificity of aminoaciduria and diagnosis of occult diseaseV M Riccardi, V E Shih, L B Holmes, et al.
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.
The New England Journal of Medicine|October 18, 1984
Benign methylmalonic aciduriaF D Ledley, H L Levy, V E Shih, 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.
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