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S I Goodman

Showing results (111-120 of 130) with videos related to

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Neurology|November 1, 1980
Glutaric acidemia: a metabolic disorder causing progressive choreoathetosisR L Leibel, V E Shih, S I Goodman, et al.
European Journal of Pediatrics|June 1, 1988
4-Hydroxybutyric aciduria in a patient without ataxia or convulsionsK M Gibson, G Hoffmann, W L Nyhan, et al.
Pediatrics|February 1, 1989
Acute profound dystonia in infants with glutaric acidemiaI Bergman, D Finegold, J C Gartner, et al.
Progress in Clinical and Biological Research|January 1, 1992
Molecular heterogeneity of beta-ETF deficiency in glutaric aciduria type III Colombo, S DiDonato, M Volta, et al.
Pediatric Pathology|January 1, 1990
Glutaric aciduria type II: autopsy study of a case with electron-transferring flavoprotein dehydrogenase deficiencyM Kamiya, T Eimoto, H Kishimoto, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Animal models for glutaryl-CoA dehydrogenase deficiencyD M Koeller, S Sauer, M Wajner, et al.
Journal of Inherited Metabolic Disease|May 10, 2002
D-2-Hydroxyglutaric aciduria in a patient with a severe clinical phenotype and unusual MRI findingsM Wajne, C R Vargas, C Funayama, et al.
The Journal of Pediatrics|August 1, 1983
Phenotypic variation in biotinidase deficiencyB Wolf, R E Grier, R J Allen, et al.
American Journal of Human Genetics|September 1, 1980
Antenatal diagnosis of glutaric acidemiaS I Goodman, D A Gallegos, C J Pullin, et al.
Neurology|November 1, 1990
Electron transfer flavoprotein: ubiquinone oxidoreductase (ETF:QO) deficiency in an adultR B Bell, A K Brownell, C R Roe, et al.
Pageof 13

Showing results (111-120 of 130) with videos related to

Sort By:
Pageof 13
Neurology|November 1, 1980
Glutaric acidemia: a metabolic disorder causing progressive choreoathetosisR L Leibel, V E Shih, S I Goodman, et al.
European Journal of Pediatrics|June 1, 1988
4-Hydroxybutyric aciduria in a patient without ataxia or convulsionsK M Gibson, G Hoffmann, W L Nyhan, et al.
Pediatrics|February 1, 1989
Acute profound dystonia in infants with glutaric acidemiaI Bergman, D Finegold, J C Gartner, et al.
Progress in Clinical and Biological Research|January 1, 1992
Molecular heterogeneity of beta-ETF deficiency in glutaric aciduria type III Colombo, S DiDonato, M Volta, et al.
Pediatric Pathology|January 1, 1990
Glutaric aciduria type II: autopsy study of a case with electron-transferring flavoprotein dehydrogenase deficiencyM Kamiya, T Eimoto, H Kishimoto, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Animal models for glutaryl-CoA dehydrogenase deficiencyD M Koeller, S Sauer, M Wajner, et al.
Journal of Inherited Metabolic Disease|May 10, 2002
D-2-Hydroxyglutaric aciduria in a patient with a severe clinical phenotype and unusual MRI findingsM Wajne, C R Vargas, C Funayama, et al.
The Journal of Pediatrics|August 1, 1983
Phenotypic variation in biotinidase deficiencyB Wolf, R E Grier, R J Allen, et al.
American Journal of Human Genetics|September 1, 1980
Antenatal diagnosis of glutaric acidemiaS I Goodman, D A Gallegos, C J Pullin, et al.
Neurology|November 1, 1990
Electron transfer flavoprotein: ubiquinone oxidoreductase (ETF:QO) deficiency in an adultR B Bell, A K Brownell, C R Roe, et al.
Pageof 13