V E Shih|J W Littlefield - JoVE Visualize

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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.

Proceedings of the National Academy of Sciences of the United States of America|January 3, 2001

Human embryonic germ cell derivatives express a broad range of developmentally distinct markers and proliferate extensively in vitroM J Shamblott, J Axelman, J W Littlefield, 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.

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Showing results (51-60 of 94) with videos related to

Sort By:

Pageof 10

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.

Proceedings of the National Academy of Sciences of the United States of America|January 3, 2001

Human embryonic germ cell derivatives express a broad range of developmentally distinct markers and proliferate extensively in vitroM J Shamblott, J Axelman, J W Littlefield, 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.

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