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J Rhead

Showing results (41-50 of 66) with videos related to

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The New England Journal of Medicine|June 1, 2007
Survival after treatment with phenylacetate and benzoate for urea-cycle disordersGregory M Enns, Susan A Berry, Gerard T Berry, et al.
Pediatric Research|August 14, 1998
Analysis of carnitine esters by radio-high performance liquid chromatography in cultured skin fibroblasts from patients with mitochondrial fatty acid oxidation disordersE Schmidt-Sommerfeld, P J Bobrowski, D Penn, et al.
Pediatric Research|May 1, 1989
Peroxisomal L-pipecolic acid oxidation is deficient in liver from Zellweger syndrome patientsS J Mihalik, H W Moser, P A Watkins, et al.
Pediatric Research|April 1, 1987
Clinical and biochemical variation and family studies in the multiple acyl-CoA dehydrogenation disordersW J Rhead, J A Wolff, M Lipson, et al.
Neurology|March 1, 1990
Juvenile multiple sclerosis-like episodes associated with a defect of mitochondrial beta oxidationB R Powell, N G Kennaway, W J Rhead, et al.
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.
Lancet (London, England)|October 21, 1978
Cannabis, hypochlorhydria, and choleraD R Nalin, M M Levine, 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.
Pageof 7

Showing results (41-50 of 66) with videos related to

Sort By:
Pageof 7
The New England Journal of Medicine|June 1, 2007
Survival after treatment with phenylacetate and benzoate for urea-cycle disordersGregory M Enns, Susan A Berry, Gerard T Berry, et al.
Pediatric Research|August 14, 1998
Analysis of carnitine esters by radio-high performance liquid chromatography in cultured skin fibroblasts from patients with mitochondrial fatty acid oxidation disordersE Schmidt-Sommerfeld, P J Bobrowski, D Penn, et al.
Pediatric Research|May 1, 1989
Peroxisomal L-pipecolic acid oxidation is deficient in liver from Zellweger syndrome patientsS J Mihalik, H W Moser, P A Watkins, et al.
Pediatric Research|April 1, 1987
Clinical and biochemical variation and family studies in the multiple acyl-CoA dehydrogenation disordersW J Rhead, J A Wolff, M Lipson, et al.
Neurology|March 1, 1990
Juvenile multiple sclerosis-like episodes associated with a defect of mitochondrial beta oxidationB R Powell, N G Kennaway, W J Rhead, et al.
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.
Lancet (London, England)|October 21, 1978
Cannabis, hypochlorhydria, and choleraD R Nalin, M M Levine, 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.
Pageof 7