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V E Shih

Showing results (51-60 of 112) with videos related to

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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.
Pediatric Research|June 1, 1972
Arginase deficiency in Macaca fascicularis. I. Arginase activity and arginine concentration in erythrocytes and liverV E Shih, T C Jones, H L Levy, et al.
The Journal of Pediatrics|April 1, 1979
Thiamine-responsive intermittent branched-chain ketoaciduriaS M Pueschel, M J Bresnan, V E Shih, 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.
Journal of Inherited Metabolic Disease|January 1, 1987
Lethal ornithine transcarbamylase deficiency in a female neonateN Girgis, V McGravey, B L Shah, et al.
JAMA|February 26, 1982
Encephalopathy following jejunoileostomyD B Carr, V E Shih, J M Richter, et al.
The Journal of Pediatrics|July 1, 1984
Maternal isovaleric acidemiaV E Shih, R H Aubry, G DeGrande, et al.
Pageof 12

Showing results (51-60 of 112) with videos related to

Sort By:
Pageof 12
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.
Pediatric Research|June 1, 1972
Arginase deficiency in Macaca fascicularis. I. Arginase activity and arginine concentration in erythrocytes and liverV E Shih, T C Jones, H L Levy, et al.
The Journal of Pediatrics|April 1, 1979
Thiamine-responsive intermittent branched-chain ketoaciduriaS M Pueschel, M J Bresnan, V E Shih, 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.
Journal of Inherited Metabolic Disease|January 1, 1987
Lethal ornithine transcarbamylase deficiency in a female neonateN Girgis, V McGravey, B L Shah, et al.
JAMA|February 26, 1982
Encephalopathy following jejunoileostomyD B Carr, V E Shih, J M Richter, et al.
The Journal of Pediatrics|July 1, 1984
Maternal isovaleric acidemiaV E Shih, R H Aubry, G DeGrande, et al.
Pageof 12