Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

V E Shih

Showing results (71-80 of 112) with videos related to

Pageof 12
Sort By:
The Journal of Clinical Investigation|September 1, 1976
Type II hyperprolinemia. Delta1-pyrroline-5-carboxylic acid dehydrogenase deficiency in cultured skin fibroblasts and circulating lymphocytesD Valle, S I Goodman, D A Applegarth, et al.
Human Molecular Genetics|November 1, 1993
Molecular basis of cystathionine beta-synthase deficiency in pyridoxine responsive and nonresponsive homocystinuriaF L Hu, Z Gu, V Kozich, et al.
American Journal of Medical Genetics|August 1, 1991
Dietary management reverses grooving and abnormal polarization of hair shafts in argininosuccinase deficiencyJ C Kvedar, H P Baden, L A Baden, et al.
The New England Journal of Medicine|October 13, 1977
Sepsis due to Escherichia coli in neonates with galactosemiaH L Levy, S J Sepe, V E Shih, et al.
Gastroenterology|October 1, 1971
Studies of intestinal transport defect in Hartnup diseaseV E Shih, E M Bixby, D H Alpers, et al.
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.)|April 1, 1971
Phenylalanine tolerance tests in simian primatesT C Jones, H L Levy, R A MacCeady, et al.
American Journal of Medical Genetics|February 1, 1989
Potential for the prenatal diagnosis of hyperornithinemia, hyperammonemia, and homocitrullinuria syndromeB Chadefaux, J P Bonnefont, D Rabier, et al.
The New England Journal of Medicine|January 31, 1985
Lysinuric protein intolerance presenting as childhood osteoporosis. Clinical and skeletal response to citrulline therapyT O Carpenter, H L Levy, M E Holtrop, et al.
Annals of Surgery|September 1, 1974
Amino acid metabolism in acute renal failure: influence of intravenous essential L-amino acid hyperalimentation therapyR M Abel, V E Shih, W M Abbott, et al.
Biochemical and Biophysical Research Communications|January 31, 1972
Homocystinuria associated with decreased methylenetetrahydrofolate reductase activityS H Mudd, B W Uhlendorf, J M Freeman, et al.
Pageof 12

Showing results (71-80 of 112) with videos related to

Sort By:
Pageof 12
The Journal of Clinical Investigation|September 1, 1976
Type II hyperprolinemia. Delta1-pyrroline-5-carboxylic acid dehydrogenase deficiency in cultured skin fibroblasts and circulating lymphocytesD Valle, S I Goodman, D A Applegarth, et al.
Human Molecular Genetics|November 1, 1993
Molecular basis of cystathionine beta-synthase deficiency in pyridoxine responsive and nonresponsive homocystinuriaF L Hu, Z Gu, V Kozich, et al.
American Journal of Medical Genetics|August 1, 1991
Dietary management reverses grooving and abnormal polarization of hair shafts in argininosuccinase deficiencyJ C Kvedar, H P Baden, L A Baden, et al.
The New England Journal of Medicine|October 13, 1977
Sepsis due to Escherichia coli in neonates with galactosemiaH L Levy, S J Sepe, V E Shih, et al.
Gastroenterology|October 1, 1971
Studies of intestinal transport defect in Hartnup diseaseV E Shih, E M Bixby, D H Alpers, et al.
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.)|April 1, 1971
Phenylalanine tolerance tests in simian primatesT C Jones, H L Levy, R A MacCeady, et al.
American Journal of Medical Genetics|February 1, 1989
Potential for the prenatal diagnosis of hyperornithinemia, hyperammonemia, and homocitrullinuria syndromeB Chadefaux, J P Bonnefont, D Rabier, et al.
The New England Journal of Medicine|January 31, 1985
Lysinuric protein intolerance presenting as childhood osteoporosis. Clinical and skeletal response to citrulline therapyT O Carpenter, H L Levy, M E Holtrop, et al.
Annals of Surgery|September 1, 1974
Amino acid metabolism in acute renal failure: influence of intravenous essential L-amino acid hyperalimentation therapyR M Abel, V E Shih, W M Abbott, et al.
Biochemical and Biophysical Research Communications|January 31, 1972
Homocystinuria associated with decreased methylenetetrahydrofolate reductase activityS H Mudd, B W Uhlendorf, J M Freeman, et al.
Pageof 12