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I Goodman

Showing results (191-200 of 347) with videos related to

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CNS Neuroscience & Therapeutics|January 15, 2010
Switching from oral cholinesterase inhibitors to the rivastigmine transdermal patchC Sadowsky, J A Davila Perez, R W Bouchard, et al.
Life Sciences|July 14, 1986
Effect of chronic uremia on the cardiovascular alpha 1 receptorL G Meggs, J Ben-Ari, D Gammon, et al.
Genomics|May 1, 1994
Assignment of human glutaryl-CoA dehydrogenase gene (GCDH) to the short arm of chromosome 19 (19p13.2) by in situ hybridization and somatic cell hybrid analysisC R Greenberg, A M Duncan, C A Gregory, et al.
Clinical Chemistry|December 26, 2001
Addition of quantitative 3-hydroxy-octadecanoic acid to the stable isotope gas chromatography-mass spectrometry method for measuring 3-hydroxy fatty acidsPatricia M Jones, Susan Tjoa, Paul V Fennessey, et al.
The New England Journal of Medicine|January 20, 1983
Deficient biotinidase activity in late-onset multiple carboxylase deficiencyB Wolf, R E Grier, W D Parker, et al.
Lancet (London, England)|November 25, 1972
X-linked transmission of ornithine-transcarbamylase deficiencyC R Scott, C C Teng, S I Goodman, et al.
Clinical Endocrinology|February 1, 1985
Pituitary Cushing's disease arising from a previously non-functional corticotrophic chromophobe adenomaN J Vaughan, C M Laroche, I Goodman, et al.
Journal of Cellular Biochemistry|December 1, 1996
Quantitative measurement of heme oxygenase-1 in the human renal adenocarcinomaA I Goodman, M Choudhury, J L da Silva, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Atypical riboflavin-responsive glutaric aciduria, and deficient peroxisomal glutaryl-CoA oxidase activity: a new peroxisomal disorderM J Bennett, R J Pollitt, S I Goodman, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 15, 1983
Biotinidase deficiency: the enzymatic defect in late-onset multiple carboxylase deficiencyB Wolf, R E Grier, R J Allen, et al.
Pageof 35

Showing results (191-200 of 347) with videos related to

Sort By:
Pageof 35
CNS Neuroscience & Therapeutics|January 15, 2010
Switching from oral cholinesterase inhibitors to the rivastigmine transdermal patchC Sadowsky, J A Davila Perez, R W Bouchard, et al.
Life Sciences|July 14, 1986
Effect of chronic uremia on the cardiovascular alpha 1 receptorL G Meggs, J Ben-Ari, D Gammon, et al.
Genomics|May 1, 1994
Assignment of human glutaryl-CoA dehydrogenase gene (GCDH) to the short arm of chromosome 19 (19p13.2) by in situ hybridization and somatic cell hybrid analysisC R Greenberg, A M Duncan, C A Gregory, et al.
Clinical Chemistry|December 26, 2001
Addition of quantitative 3-hydroxy-octadecanoic acid to the stable isotope gas chromatography-mass spectrometry method for measuring 3-hydroxy fatty acidsPatricia M Jones, Susan Tjoa, Paul V Fennessey, et al.
The New England Journal of Medicine|January 20, 1983
Deficient biotinidase activity in late-onset multiple carboxylase deficiencyB Wolf, R E Grier, W D Parker, et al.
Lancet (London, England)|November 25, 1972
X-linked transmission of ornithine-transcarbamylase deficiencyC R Scott, C C Teng, S I Goodman, et al.
Clinical Endocrinology|February 1, 1985
Pituitary Cushing's disease arising from a previously non-functional corticotrophic chromophobe adenomaN J Vaughan, C M Laroche, I Goodman, et al.
Journal of Cellular Biochemistry|December 1, 1996
Quantitative measurement of heme oxygenase-1 in the human renal adenocarcinomaA I Goodman, M Choudhury, J L da Silva, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Atypical riboflavin-responsive glutaric aciduria, and deficient peroxisomal glutaryl-CoA oxidase activity: a new peroxisomal disorderM J Bennett, R J Pollitt, S I Goodman, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 15, 1983
Biotinidase deficiency: the enzymatic defect in late-onset multiple carboxylase deficiencyB Wolf, R E Grier, R J Allen, et al.
Pageof 35