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P T Clayton

Showing results (71-80 of 101) with videos related to

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Archives of Disease in Childhood|October 1, 1993
Cystic fibrosis presenting as kwashiorkor with florid skin rashR J Phillips, C M Crock, M J Dillon, et al.
Lancet (London, England)|February 14, 1987
Ultrastructure of liver in inherited disorders of fat oxidationB D Lake, P T Clayton, J V Leonard, et al.
The British Journal of Ophthalmology|April 1, 1989
Leber's congenital amaurosis--a new syndrome with a cardiomyopathyI M Russell-Eggitt, D S Taylor, P T Clayton, et al.
European Journal of Pediatrics|May 1, 1991
Pellagra with colitis due to a defect in tryptophan metabolismP T Clayton, N A Bridges, D J Atherton, et al.
Gut|September 13, 2003
Mutations in SRD5B1 (AKR1D1), the gene encoding delta(4)-3-oxosteroid 5beta-reductase, in hepatitis and liver failure in infancyH A Lemonde, E J Custard, J Bouquet, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Isolated dihydroxyacetonephosphate acyltransferase deficiency presenting with developmental delayP T Clayton, S Eckhardt, J Wilson, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Ataxia associated with increased plasma concentrations of pristanic acid, phytanic acid and C27 bile acids but normal fibroblast branched-chain fatty acid oxidationP T Clayton, A W Johnson, K A Mills, et al.
The Journal of Clinical Investigation|April 1, 1987
Familial giant cell hepatitis associated with synthesis of 3 beta, 7 alpha-dihydroxy-and 3 beta,7 alpha, 12 alpha-trihydroxy-5-cholenoic acidsP T Clayton, J V Leonard, A M Lawson, et al.
European Journal of Pediatrics|March 1, 1987
Plasma bile acids in patients with peroxisomal dysfunction syndromes: analysis by capillary gas chromatography-mass spectrometryP T Clayton, B D Lake, N A Hall, et al.
Neuroscience Letters|February 21, 2015
The Fabry disease-associated lipid Lyso-Gb3 enhances voltage-gated calcium currents in sensory neurons and causes painL Choi, J Vernon, O Kopach, et al.
Pageof 11

Showing results (71-80 of 101) with videos related to

Sort By:
Pageof 11
Archives of Disease in Childhood|October 1, 1993
Cystic fibrosis presenting as kwashiorkor with florid skin rashR J Phillips, C M Crock, M J Dillon, et al.
Lancet (London, England)|February 14, 1987
Ultrastructure of liver in inherited disorders of fat oxidationB D Lake, P T Clayton, J V Leonard, et al.
The British Journal of Ophthalmology|April 1, 1989
Leber's congenital amaurosis--a new syndrome with a cardiomyopathyI M Russell-Eggitt, D S Taylor, P T Clayton, et al.
European Journal of Pediatrics|May 1, 1991
Pellagra with colitis due to a defect in tryptophan metabolismP T Clayton, N A Bridges, D J Atherton, et al.
Gut|September 13, 2003
Mutations in SRD5B1 (AKR1D1), the gene encoding delta(4)-3-oxosteroid 5beta-reductase, in hepatitis and liver failure in infancyH A Lemonde, E J Custard, J Bouquet, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Isolated dihydroxyacetonephosphate acyltransferase deficiency presenting with developmental delayP T Clayton, S Eckhardt, J Wilson, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Ataxia associated with increased plasma concentrations of pristanic acid, phytanic acid and C27 bile acids but normal fibroblast branched-chain fatty acid oxidationP T Clayton, A W Johnson, K A Mills, et al.
The Journal of Clinical Investigation|April 1, 1987
Familial giant cell hepatitis associated with synthesis of 3 beta, 7 alpha-dihydroxy-and 3 beta,7 alpha, 12 alpha-trihydroxy-5-cholenoic acidsP T Clayton, J V Leonard, A M Lawson, et al.
European Journal of Pediatrics|March 1, 1987
Plasma bile acids in patients with peroxisomal dysfunction syndromes: analysis by capillary gas chromatography-mass spectrometryP T Clayton, B D Lake, N A Hall, et al.
Neuroscience Letters|February 21, 2015
The Fabry disease-associated lipid Lyso-Gb3 enhances voltage-gated calcium currents in sensory neurons and causes painL Choi, J Vernon, O Kopach, et al.
Pageof 11