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The American Review of Respiratory Disease
|
August 1, 1985
Relationship between central nervous system hydrogen ion regulation and amino acid metabolism in hypercapnia, II
B Hoop, V E Shih, H Kazemi
Journal of Inherited Metabolic Disease
|
January 1, 1981
Defective ornithine metabolism in the syndrome of hyperornithinaemia, hyperammonaemia and homocitrullinuria
V E Shih, R Mandell, A Herzfeld
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
November 15, 1973
Diagnosis of isovaleric acidemia in cultured fibroblasts
V E Shih, R Mandell, K Tanaka
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 5, 1982
Defective ornithine metabolism in cultured skin fibroblasts from patients with the syndrome of hyperornithinemia, hyperammonemia and homocitrullinuria
V E Shih, R Mandell, A Herzfeld
American Journal of Human Genetics
|
December 1, 1988
Pyridoxine effects on ornithine ketoacid transaminase activity in fibroblasts from carriers of two forms of gyrate atrophy of the choroid and retina
V E Shih, R Mandell, E L Berson
Clinical Chemistry
|
January 1, 1985
Acetaminophen metabolite interferes in analysis for amino acids
V E Shih, V Nikiforov, M M Carney
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
July 1, 1981
Reduction of hyperornithinemia with a low protein, low arginine diet and pyridoxine in patients with a deficiency of ornithine-ketoacid transaminase (OKT) activity and gyrate atrophy of the choroid and retina
V E Shih, E L Berson, M Gargiulo
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
July 2, 1979
A simple screening test for sulfite oxidase deficiency: detection of urinary thiosulfate by a modification of Sörbo's method
V E Shih, M M Carney, R Mandell
Molecular Biology & Medicine
|
February 1, 1991
Molecular pathology of gyrate atrophy of the choroid and retina due to ornithine aminotransferase deficiency
V Ramesh, J F Gusella, V E Shih
Archives of Neurology
|
October 1, 1990
Episodic hyperammonemia in adult siblings with hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome
M Tuchman, D S Knopman, V E Shih
Page
of 12
Search research articles
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Showing results (21-30 of 112) with videos related to
Sort By:
Page
of 12
The American Review of Respiratory Disease
|
August 1, 1985
Relationship between central nervous system hydrogen ion regulation and amino acid metabolism in hypercapnia, II
B Hoop, V E Shih, H Kazemi
Journal of Inherited Metabolic Disease
|
January 1, 1981
Defective ornithine metabolism in the syndrome of hyperornithinaemia, hyperammonaemia and homocitrullinuria
V E Shih, R Mandell, A Herzfeld
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
November 15, 1973
Diagnosis of isovaleric acidemia in cultured fibroblasts
V E Shih, R Mandell, K Tanaka
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 5, 1982
Defective ornithine metabolism in cultured skin fibroblasts from patients with the syndrome of hyperornithinemia, hyperammonemia and homocitrullinuria
V E Shih, R Mandell, A Herzfeld
American Journal of Human Genetics
|
December 1, 1988
Pyridoxine effects on ornithine ketoacid transaminase activity in fibroblasts from carriers of two forms of gyrate atrophy of the choroid and retina
V E Shih, R Mandell, E L Berson
Clinical Chemistry
|
January 1, 1985
Acetaminophen metabolite interferes in analysis for amino acids
V E Shih, V Nikiforov, M M Carney
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
July 1, 1981
Reduction of hyperornithinemia with a low protein, low arginine diet and pyridoxine in patients with a deficiency of ornithine-ketoacid transaminase (OKT) activity and gyrate atrophy of the choroid and retina
V E Shih, E L Berson, M Gargiulo
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
July 2, 1979
A simple screening test for sulfite oxidase deficiency: detection of urinary thiosulfate by a modification of Sörbo's method
V E Shih, M M Carney, R Mandell
Molecular Biology & Medicine
|
February 1, 1991
Molecular pathology of gyrate atrophy of the choroid and retina due to ornithine aminotransferase deficiency
V Ramesh, J F Gusella, V E Shih
Archives of Neurology
|
October 1, 1990
Episodic hyperammonemia in adult siblings with hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome
M Tuchman, D S Knopman, V E Shih
Page
of 12