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The New England Journal of Medicine
|
June 10, 1971
Management of hereditary metabolic disease. The role of allied health personnel
C L Clow, T M Reade, C R Scriver
Pediatrics
|
December 1, 1981
Outcome of early and long-term management of classical maple syrup urine disease
C L Clow, T M Reade, C R Scriver
The Biochemical Journal
|
August 15, 1983
Metabolism of ethylmalonate to mesaconate in the rat. Evidence for trans-dehydrogenation of methylsuccinate
J A Montgomery, O A Mamer, C R Scriver
Metabolism: Clinical and Experimental
|
August 1, 1980
Labile methyl group balances in the human: the role of sarcosine
S H Mudd, M H Ebert, C R Scriver
Annals of the New York Academy of Sciences
|
January 1, 1985
Isolation and culture of murine renal proximal tubule cells: a system to study solute transport in mutants
C L Bell, H S Tenenhouse, C R Scriver
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
October 1, 1972
Primary hyperparathyroidism and hyperaminoaciduria
D C Cusworth, C E Dent, C R Scriver
Nucleic Acids Research
|
January 1, 1996
PAH Mutation Analysis Consortium Database: a database for disease-producing and other allelic variation at the human PAH locus
L Hoang, S Byck, L Prevost, et al.
Canadian Medical Association Journal
|
November 16, 1974
Screening, counselling and treatment of hereditary metabolic disease; a survey of resources in Canada
J C Haworth, J R Miller, C R Scriver
In Vitro Cellular & Developmental Biology : Journal of the Tissue Culture Association
|
July 1, 1988
Initiation and characterization of primary mouse kidney epithelial cultures
C L Bell, H S Tenenhouse, C R Scriver
American Journal of Human Genetics
|
September 1, 1988
Primary cultures of renal epithelial cells from X-linked hypophosphatemic (Hyp) mice express defects in phosphate transport and vitamin D metabolism
C L Bell, H S Tenenhouse, C R Scriver
Page
of 32
Search research articles
Search
Showing results (171-180 of 317) with videos related to
Sort By:
Page
of 32
The New England Journal of Medicine
|
June 10, 1971
Management of hereditary metabolic disease. The role of allied health personnel
C L Clow, T M Reade, C R Scriver
Pediatrics
|
December 1, 1981
Outcome of early and long-term management of classical maple syrup urine disease
C L Clow, T M Reade, C R Scriver
The Biochemical Journal
|
August 15, 1983
Metabolism of ethylmalonate to mesaconate in the rat. Evidence for trans-dehydrogenation of methylsuccinate
J A Montgomery, O A Mamer, C R Scriver
Metabolism: Clinical and Experimental
|
August 1, 1980
Labile methyl group balances in the human: the role of sarcosine
S H Mudd, M H Ebert, C R Scriver
Annals of the New York Academy of Sciences
|
January 1, 1985
Isolation and culture of murine renal proximal tubule cells: a system to study solute transport in mutants
C L Bell, H S Tenenhouse, C R Scriver
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
October 1, 1972
Primary hyperparathyroidism and hyperaminoaciduria
D C Cusworth, C E Dent, C R Scriver
Nucleic Acids Research
|
January 1, 1996
PAH Mutation Analysis Consortium Database: a database for disease-producing and other allelic variation at the human PAH locus
L Hoang, S Byck, L Prevost, et al.
Canadian Medical Association Journal
|
November 16, 1974
Screening, counselling and treatment of hereditary metabolic disease; a survey of resources in Canada
J C Haworth, J R Miller, C R Scriver
In Vitro Cellular & Developmental Biology : Journal of the Tissue Culture Association
|
July 1, 1988
Initiation and characterization of primary mouse kidney epithelial cultures
C L Bell, H S Tenenhouse, C R Scriver
American Journal of Human Genetics
|
September 1, 1988
Primary cultures of renal epithelial cells from X-linked hypophosphatemic (Hyp) mice express defects in phosphate transport and vitamin D metabolism
C L Bell, H S Tenenhouse, C R Scriver
Page
of 32