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C R Scriver

Showing results (291-300 of 317) with videos related to

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Human Mutation|January 1, 1993
Molecular studies of mitochondrial acetoacetyl-coenzyme A thiolase deficiency in the two original familiesT Fukao, S Yamaguchi, C R Scriver, et al.
American Journal of Human Genetics|March 1, 1990
X-linked hypophosphatemia: the mutant gene is expressed in teeth as well as in kidneyE D Shields, C R Scriver, T Reade, et al.
L'Union Medicale Du Canada|August 1, 1988
[The beta-thalassemia gene in French Canada: reappearance in Portneuf County]C Prévost, R Laframboise, M Bardanis, et al.
Pediatric Research|April 1, 1973
The effect of intravenous glucagon on plasma amino acids in the newbornS H Reisner, J V Aranda, E Colle, et al.
The Journal of Pediatrics|March 1, 1985
Ontogeny modifies manifestations of cystinuria genes: implications for counselingC R Scriver, C L Clow, T M Reade, et al.
Human Mutation|January 1, 1992
Novel Tay-Sachs disease mutations from ChinaN Akalin, H P Shi, G Vavougios, et al.
The Journal of Pediatrics|July 1, 1992
Brain dysgenesis and congenital intracerebral calcification associated with 3-hydroxyisobutyric aciduriaD Chitayat, K Meagher-Villemure, O A Mamer, et al.
Pediatric Research|October 6, 1997
Analysis of phenylalanine hydroxylase genotypes and hyperphenylalaninemia phenotypes using L-[1-13C]phenylalanine oxidation rates in vivo: a pilot studyE P Treacy, J J Delente, G Elkas, et al.
Pediatrics|January 1, 1981
Metabolic abnormalities in the idiopathic Fanconi syndrome: studies of carbohydrate metabolism in two patientsR W Chesney, B S Kaplan, D Teitel, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 3, 1999
A different approach to treatment of phenylketonuria: phenylalanine degradation with recombinant phenylalanine ammonia lyaseC N Sarkissian, Z Shao, F Blain, et al.
Pageof 32

Showing results (291-300 of 317) with videos related to

Sort By:
Pageof 32
Human Mutation|January 1, 1993
Molecular studies of mitochondrial acetoacetyl-coenzyme A thiolase deficiency in the two original familiesT Fukao, S Yamaguchi, C R Scriver, et al.
American Journal of Human Genetics|March 1, 1990
X-linked hypophosphatemia: the mutant gene is expressed in teeth as well as in kidneyE D Shields, C R Scriver, T Reade, et al.
L'Union Medicale Du Canada|August 1, 1988
[The beta-thalassemia gene in French Canada: reappearance in Portneuf County]C Prévost, R Laframboise, M Bardanis, et al.
Pediatric Research|April 1, 1973
The effect of intravenous glucagon on plasma amino acids in the newbornS H Reisner, J V Aranda, E Colle, et al.
The Journal of Pediatrics|March 1, 1985
Ontogeny modifies manifestations of cystinuria genes: implications for counselingC R Scriver, C L Clow, T M Reade, et al.
Human Mutation|January 1, 1992
Novel Tay-Sachs disease mutations from ChinaN Akalin, H P Shi, G Vavougios, et al.
The Journal of Pediatrics|July 1, 1992
Brain dysgenesis and congenital intracerebral calcification associated with 3-hydroxyisobutyric aciduriaD Chitayat, K Meagher-Villemure, O A Mamer, et al.
Pediatric Research|October 6, 1997
Analysis of phenylalanine hydroxylase genotypes and hyperphenylalaninemia phenotypes using L-[1-13C]phenylalanine oxidation rates in vivo: a pilot studyE P Treacy, J J Delente, G Elkas, et al.
Pediatrics|January 1, 1981
Metabolic abnormalities in the idiopathic Fanconi syndrome: studies of carbohydrate metabolism in two patientsR W Chesney, B S Kaplan, D Teitel, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 3, 1999
A different approach to treatment of phenylketonuria: phenylalanine degradation with recombinant phenylalanine ammonia lyaseC N Sarkissian, Z Shao, F Blain, et al.
Pageof 32