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L Sweetman

Showing results (151-160 of 175) with videos related to

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Journal of Inherited Metabolic Disease|March 1, 1997
An unusual case of multiple carboxylase deficiency presenting as generalized pustular psoriasis in a Chinese boyL K Law, C Y Lau, C P Pang, et al.
American Journal of Medical Genetics|September 1, 1992
Hawkinsinuria in two familiesM Borden, J Holm, J Leslie, et al.
Journal of Child Neurology|March 1, 1995
D-2-hydroxyglutaric aciduriaW L Nyhan, G D Shelton, C Jakobs, et al.
Molecular Genetics and Metabolism|April 18, 2000
Identification of a novel mutation in patients with medium-chain acyl-CoA dehydrogenase deficiencyB Z Yang, J H Ding, C Zhou, et al.
Progress in Clinical and Biological Research|January 1, 1990
3-Ketothiolase deficiency: molecular heterogeneity of the enzyme defect and cloning of the cDNAS Yamaguchi, T Fukao, H Nagasawa, et al.
European Journal of Pediatrics|April 1, 1986
3-Ketothiolase deficiencyB Middleton, K Bartlett, A Romanos, et al.
Lancet (London, England)|June 26, 1982
Prenatal treatment of biotin responsive multiple carboxylase deficiencyS Packman, M J Cowan, M S Golbus, et al.
Pediatric Research|July 1, 1991
Metabolism of 1-13C-propionate in vivo in patients with disorders of propionate metabolismB A Barshop, I Yoshida, A Ajami, et al.
Equine Veterinary Journal|November 22, 2012
Seasonal pasture myopathy/atypical myopathy in North America associated with ingestion of hypoglycin A within seeds of the box elder treeS J Valberg, B T Sponseller, A D Hegeman, et al.
American Journal of Medical Genetics|February 1, 1990
Transcobalamin II deficiency presenting with methylmalonic aciduria and homocystinuria and abnormal absorption of cobalaminB A Barshop, J Wolff, W L Nyhan, et al.
Pageof 18

Showing results (151-160 of 175) with videos related to

Sort By:
Pageof 18
Journal of Inherited Metabolic Disease|March 1, 1997
An unusual case of multiple carboxylase deficiency presenting as generalized pustular psoriasis in a Chinese boyL K Law, C Y Lau, C P Pang, et al.
American Journal of Medical Genetics|September 1, 1992
Hawkinsinuria in two familiesM Borden, J Holm, J Leslie, et al.
Journal of Child Neurology|March 1, 1995
D-2-hydroxyglutaric aciduriaW L Nyhan, G D Shelton, C Jakobs, et al.
Molecular Genetics and Metabolism|April 18, 2000
Identification of a novel mutation in patients with medium-chain acyl-CoA dehydrogenase deficiencyB Z Yang, J H Ding, C Zhou, et al.
Progress in Clinical and Biological Research|January 1, 1990
3-Ketothiolase deficiency: molecular heterogeneity of the enzyme defect and cloning of the cDNAS Yamaguchi, T Fukao, H Nagasawa, et al.
European Journal of Pediatrics|April 1, 1986
3-Ketothiolase deficiencyB Middleton, K Bartlett, A Romanos, et al.
Lancet (London, England)|June 26, 1982
Prenatal treatment of biotin responsive multiple carboxylase deficiencyS Packman, M J Cowan, M S Golbus, et al.
Pediatric Research|July 1, 1991
Metabolism of 1-13C-propionate in vivo in patients with disorders of propionate metabolismB A Barshop, I Yoshida, A Ajami, et al.
Equine Veterinary Journal|November 22, 2012
Seasonal pasture myopathy/atypical myopathy in North America associated with ingestion of hypoglycin A within seeds of the box elder treeS J Valberg, B T Sponseller, A D Hegeman, et al.
American Journal of Medical Genetics|February 1, 1990
Transcobalamin II deficiency presenting with methylmalonic aciduria and homocystinuria and abnormal absorption of cobalaminB A Barshop, J Wolff, W L Nyhan, et al.
Pageof 18