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G A Mitchell

Showing results (81-90 of 110) with videos related to

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Biochemical Society Transactions|July 3, 1998
Inborn errors of ketogenesisG A Mitchell, S P Wang, L Ashmarina, et al.
The Journal of Pediatrics|March 1, 1986
Clinical heterogeneity in cobalamin C variant of combined homocystinuria and methylmalonic aciduriaG A Mitchell, D Watkins, S B Melançon, et al.
Human Mutation|January 1, 1995
Molecular, biochemical, and clinical characterization of mitochondrial acetoacetyl-coenzyme A thiolase deficiency in two further patientsA Wakazono, T Fukao, S Yamaguchi, et al.
The Journal of Biological Chemistry|October 5, 1988
Human ornithine-delta-aminotransferase. cDNA cloning and analysis of the structural geneG A Mitchell, J E Looney, L C Brody, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Fatal cardiomyopathy associated with 3-hydroxy-3-methylglutaryl-CoA lyase deficiencyK M Gibson, S B Cassidy, L H Seaver, et al.
The Journal of Clinical Investigation|February 1, 1988
An initiator codon mutation in ornithine-delta-aminotransferase causing gyrate atrophy of the choroid and retinaG A Mitchell, L C Brody, J Looney, et al.
Clinical and Investigative Medicine. Medecine Clinique Et Experimentale|June 1, 1995
Medical aspects of ketone body metabolismG A Mitchell, S Kassovska-Bratinova, Y Boukaftane, et al.
Human Molecular Genetics|July 13, 2001
Sim1 haploinsufficiency causes hyperphagia, obesity and reduction of the paraventricular nucleus of the hypothalamusJ L Michaud, F Boucher, A Melnyk, et al.
Obesity Research|April 24, 2001
The adipose tissue phenotype of hormone-sensitive lipase deficiency in miceS P Wang, N Laurin, J Himms-Hagen, et al.
Journal of Medical Genetics|November 4, 2008
Phenotypic variability among patients with hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome homozygous for the delF188 mutation in SLC25A15F-G Debray, M Lambert, B Lemieux, et al.
Pageof 11

Showing results (81-90 of 110) with videos related to

Sort By:
Pageof 11
Biochemical Society Transactions|July 3, 1998
Inborn errors of ketogenesisG A Mitchell, S P Wang, L Ashmarina, et al.
The Journal of Pediatrics|March 1, 1986
Clinical heterogeneity in cobalamin C variant of combined homocystinuria and methylmalonic aciduriaG A Mitchell, D Watkins, S B Melançon, et al.
Human Mutation|January 1, 1995
Molecular, biochemical, and clinical characterization of mitochondrial acetoacetyl-coenzyme A thiolase deficiency in two further patientsA Wakazono, T Fukao, S Yamaguchi, et al.
The Journal of Biological Chemistry|October 5, 1988
Human ornithine-delta-aminotransferase. cDNA cloning and analysis of the structural geneG A Mitchell, J E Looney, L C Brody, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Fatal cardiomyopathy associated with 3-hydroxy-3-methylglutaryl-CoA lyase deficiencyK M Gibson, S B Cassidy, L H Seaver, et al.
The Journal of Clinical Investigation|February 1, 1988
An initiator codon mutation in ornithine-delta-aminotransferase causing gyrate atrophy of the choroid and retinaG A Mitchell, L C Brody, J Looney, et al.
Clinical and Investigative Medicine. Medecine Clinique Et Experimentale|June 1, 1995
Medical aspects of ketone body metabolismG A Mitchell, S Kassovska-Bratinova, Y Boukaftane, et al.
Human Molecular Genetics|July 13, 2001
Sim1 haploinsufficiency causes hyperphagia, obesity and reduction of the paraventricular nucleus of the hypothalamusJ L Michaud, F Boucher, A Melnyk, et al.
Obesity Research|April 24, 2001
The adipose tissue phenotype of hormone-sensitive lipase deficiency in miceS P Wang, N Laurin, J Himms-Hagen, et al.
Journal of Medical Genetics|November 4, 2008
Phenotypic variability among patients with hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome homozygous for the delF188 mutation in SLC25A15F-G Debray, M Lambert, B Lemieux, et al.
Pageof 11