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W J Rhead

Showing results (51-60 of 65) with videos related to

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The Journal of Clinical Investigation|May 1, 1987
Short-chain acyl-coenzyme A dehydrogenase deficiency. Clinical and biochemical studies in two patientsB A Amendt, C Greene, L Sweetman, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 1, 1992
Neuropsychiatric manifestations of defect in mitochondrial beta oxidation response to riboflavinW J Triggs, C R Roe, W J Rhead, et al.
Nature Genetics|November 1, 1996
Mutations in the glutathione synthetase gene cause 5-oxoprolinuriaZ Z Shi, G M Habib, W J Rhead, et al.
Biochemical and Biophysical Research Communications|March 31, 1993
A novel disease with deficiency of mitochondrial very-long-chain acyl-CoA dehydrogenaseT Aoyama, Y Uchida, R I Kelley, et al.
The Journal of Clinical Investigation|June 1, 1995
Purification of human very-long-chain acyl-coenzyme A dehydrogenase and characterization of its deficiency in seven patientsT Aoyama, M Souri, S Ushikubo, et al.
Human Molecular Genetics|September 1, 1997
Functional correction of short-chain acyl-CoA dehydrogenase deficiency in transgenic mice: implications for gene therapy of human mitochondrial enzyme deficienciesC L Kelly, W J Rhead, W K Kutschke, et al.
The Journal of Pediatrics|July 1, 1989
Mitochondrial encephalomyopathy with associated aminoacidopathy in a male sibshipF A Booth, J C Haworth, L A Dilling, et al.
Pediatric Neurology|March 1, 1991
Defect in fatty acid oxidation: laboratory and pathologic findings in a patientJ H Tonsgard, J K Stephens, W J Rhead, et al.
Biochemical and Biophysical Research Communications|August 31, 1990
Identification of a common mutation in patients with medium-chain acyl-CoA dehydrogenase deficiencyY Matsubara, K Narisawa, S Miyabayashi, et al.
American Journal of Obstetrics and Gynecology|April 16, 1999
Undiagnosed maternal phenylketonuria: the need for prenatal selective screening or case findingW B Hanley, L D Platt, R P Bachman, et al.
Pageof 7

Showing results (51-60 of 65) with videos related to

Sort By:
Pageof 7
The Journal of Clinical Investigation|May 1, 1987
Short-chain acyl-coenzyme A dehydrogenase deficiency. Clinical and biochemical studies in two patientsB A Amendt, C Greene, L Sweetman, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 1, 1992
Neuropsychiatric manifestations of defect in mitochondrial beta oxidation response to riboflavinW J Triggs, C R Roe, W J Rhead, et al.
Nature Genetics|November 1, 1996
Mutations in the glutathione synthetase gene cause 5-oxoprolinuriaZ Z Shi, G M Habib, W J Rhead, et al.
Biochemical and Biophysical Research Communications|March 31, 1993
A novel disease with deficiency of mitochondrial very-long-chain acyl-CoA dehydrogenaseT Aoyama, Y Uchida, R I Kelley, et al.
The Journal of Clinical Investigation|June 1, 1995
Purification of human very-long-chain acyl-coenzyme A dehydrogenase and characterization of its deficiency in seven patientsT Aoyama, M Souri, S Ushikubo, et al.
Human Molecular Genetics|September 1, 1997
Functional correction of short-chain acyl-CoA dehydrogenase deficiency in transgenic mice: implications for gene therapy of human mitochondrial enzyme deficienciesC L Kelly, W J Rhead, W K Kutschke, et al.
The Journal of Pediatrics|July 1, 1989
Mitochondrial encephalomyopathy with associated aminoacidopathy in a male sibshipF A Booth, J C Haworth, L A Dilling, et al.
Pediatric Neurology|March 1, 1991
Defect in fatty acid oxidation: laboratory and pathologic findings in a patientJ H Tonsgard, J K Stephens, W J Rhead, et al.
Biochemical and Biophysical Research Communications|August 31, 1990
Identification of a common mutation in patients with medium-chain acyl-CoA dehydrogenase deficiencyY Matsubara, K Narisawa, S Miyabayashi, et al.
American Journal of Obstetrics and Gynecology|April 16, 1999
Undiagnosed maternal phenylketonuria: the need for prenatal selective screening or case findingW B Hanley, L D Platt, R P Bachman, et al.
Pageof 7