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D M Danks

Showing results (241-250 of 255) with videos related to

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The Journal of Pediatrics|October 1, 1977
Iminopeptiduria, skin ulcerations, and edema in a boy with prolidase deficiencyL J Sheffield, P Schlesinger, K Faull, et al.
Annals of Neurology|March 1, 1996
Leigh syndrome: clinical features and biochemical and DNA abnormalitiesS Rahman, R B Blok, H H Dahl, et al.
The New England Journal of Medicine|April 29, 1976
Letter: Patient with defect in leucine metabolismK Faull, P Bolton, B Halpern, et al.
Molecular Genetics and Metabolism|November 14, 2000
Mutations in the 4-hydroxyphenylpyruvic acid dioxygenase gene are responsible for tyrosinemia type III and hawkinsinuriaK Tomoeda, H Awata, T Matsuura, et al.
Journal of Inherited Metabolic Disease|January 1, 1978
Malignant hyperphenylalaninaemia--current status (June 1977)D M Danks, K Bartholomé, B E Clayton, et al.
The Journal of Pediatrics|June 1, 1987
Nonketotic hyperglycinemia: analyses of glycine cleavage system in typical and atypical casesK Hayasaka, K Tada, N Fueki, et al.
The New England Journal of Medicine|February 26, 1976
Dihydrofolate reductase deficiency causing megaloblastic anemia in two familiesG P Tauro, D M Danks, P B Rowe, et al.
Biomedical Mass Spectrometry|March 1, 1981
Two new sulphur-containing amino acids in manR J Truscott, D Malegan, E McCairns, et al.
Lancet (London, England)|November 28, 1992
Phenotype and genotype heterogeneity in autosomal dominant polycystic kidney diseaseD Ravine, R G Walker, R N Gibson, et al.
Pediatrics|October 1, 1982
beta-hydroxyisobutyryl coenzyme A deacylase deficiency: a defect in valine metabolism associated with physical malformationsG K Brown, S M Hunt, R Scholem, et al.
Pageof 26

Showing results (241-250 of 255) with videos related to

Sort By:
Pageof 26
The Journal of Pediatrics|October 1, 1977
Iminopeptiduria, skin ulcerations, and edema in a boy with prolidase deficiencyL J Sheffield, P Schlesinger, K Faull, et al.
Annals of Neurology|March 1, 1996
Leigh syndrome: clinical features and biochemical and DNA abnormalitiesS Rahman, R B Blok, H H Dahl, et al.
The New England Journal of Medicine|April 29, 1976
Letter: Patient with defect in leucine metabolismK Faull, P Bolton, B Halpern, et al.
Molecular Genetics and Metabolism|November 14, 2000
Mutations in the 4-hydroxyphenylpyruvic acid dioxygenase gene are responsible for tyrosinemia type III and hawkinsinuriaK Tomoeda, H Awata, T Matsuura, et al.
Journal of Inherited Metabolic Disease|January 1, 1978
Malignant hyperphenylalaninaemia--current status (June 1977)D M Danks, K Bartholomé, B E Clayton, et al.
The Journal of Pediatrics|June 1, 1987
Nonketotic hyperglycinemia: analyses of glycine cleavage system in typical and atypical casesK Hayasaka, K Tada, N Fueki, et al.
The New England Journal of Medicine|February 26, 1976
Dihydrofolate reductase deficiency causing megaloblastic anemia in two familiesG P Tauro, D M Danks, P B Rowe, et al.
Biomedical Mass Spectrometry|March 1, 1981
Two new sulphur-containing amino acids in manR J Truscott, D Malegan, E McCairns, et al.
Lancet (London, England)|November 28, 1992
Phenotype and genotype heterogeneity in autosomal dominant polycystic kidney diseaseD Ravine, R G Walker, R N Gibson, et al.
Pediatrics|October 1, 1982
beta-hydroxyisobutyryl coenzyme A deacylase deficiency: a defect in valine metabolism associated with physical malformationsG K Brown, S M Hunt, R Scholem, et al.
Pageof 26