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D M Kirby

Showing results (1-10 of 21) with videos related to

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Probe (Ottawa, Ont.)|May 1, 1996
Towards the professional status of dental hygiene in AlbertaC Lautar, D M Kirby
Bone|January 1, 1986
Urinary-free amino acids in osteogenesis imperfectaW G Cole, D M Kirby
Mitochondrion|August 27, 2005
Respiratory chain enzyme analysis in muscle and liverD R Thorburn, C W Chow, D M Kirby
European Journal of Pediatrics|March 1, 1992
Maternal tyrosinaemia II: management and successful outcomeD E Francis, D M Kirby, G N Thompson
Archives of Disease in Childhood|November 1, 1991
Pregnancy in phenylketonuria: dietary treatment aimed at normalising maternal plasma phenylalanine concentrationG N Thompson, D E Francis, D M Kirby, et al.
Analytical Chemistry|June 7, 2011
A Family of Single-Isomer Chiral Resolving Agents for Capillary Electrophoresis. 2. Hepta-6-sulfato-β-cyclodextrinJ B Vincent, D M Kirby, T V Nguyen, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Characterization of the mutations in three patients with pyruvate dehydrogenase E1 alpha deficiencyL L Hansen, G K Brown, D M Kirby, et al.
Neuropediatrics|September 3, 2005
The importance of liver biopsy in the investigation of possible mitochondrial respiratory chain diseaseJ Panetta, K Gibson, D M Kirby, et al.
European Journal of Pediatrics|September 1, 1986
Difficulties in assessing the effect of strychnine on the outcome of non-ketotic hyperglycinaemia. Observations on sisters with a mild T-protein defectE A Haan, D M Kirby, K Tada, et al.
Annals of Neurology|July 14, 2000
Leigh disease caused by the mitochondrial DNA G14459A mutation in unrelated familiesD M Kirby, S G Kahler, M L Freckmann, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Probe (Ottawa, Ont.)|May 1, 1996
Towards the professional status of dental hygiene in AlbertaC Lautar, D M Kirby
Bone|January 1, 1986
Urinary-free amino acids in osteogenesis imperfectaW G Cole, D M Kirby
Mitochondrion|August 27, 2005
Respiratory chain enzyme analysis in muscle and liverD R Thorburn, C W Chow, D M Kirby
European Journal of Pediatrics|March 1, 1992
Maternal tyrosinaemia II: management and successful outcomeD E Francis, D M Kirby, G N Thompson
Archives of Disease in Childhood|November 1, 1991
Pregnancy in phenylketonuria: dietary treatment aimed at normalising maternal plasma phenylalanine concentrationG N Thompson, D E Francis, D M Kirby, et al.
Analytical Chemistry|June 7, 2011
A Family of Single-Isomer Chiral Resolving Agents for Capillary Electrophoresis. 2. Hepta-6-sulfato-β-cyclodextrinJ B Vincent, D M Kirby, T V Nguyen, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Characterization of the mutations in three patients with pyruvate dehydrogenase E1 alpha deficiencyL L Hansen, G K Brown, D M Kirby, et al.
Neuropediatrics|September 3, 2005
The importance of liver biopsy in the investigation of possible mitochondrial respiratory chain diseaseJ Panetta, K Gibson, D M Kirby, et al.
European Journal of Pediatrics|September 1, 1986
Difficulties in assessing the effect of strychnine on the outcome of non-ketotic hyperglycinaemia. Observations on sisters with a mild T-protein defectE A Haan, D M Kirby, K Tada, et al.
Annals of Neurology|July 14, 2000
Leigh disease caused by the mitochondrial DNA G14459A mutation in unrelated familiesD M Kirby, S G Kahler, M L Freckmann, et al.
Pageof 3