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Neurology
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February 5, 1999
Short-chain acyl-CoA dehydrogenase deficiency: a cause of ophthalmoplegia and multicore myopathy
I Tein, R H Haslam, W J Rhead, et al.
Progress in Clinical and Biological Research
|
January 1, 1990
A murine model for short-chain acyl-CoA dehydrogenase deficiency
P A Wood, B A Amendt, W J Rhead, et al.
Pediatric Research
|
January 1, 1989
Short-chain acyl-coenzyme A dehydrogenase deficiency in mice
P A Wood, B A Amendt, W J Rhead, et al.
Advances in Experimental Medicine and Biology
|
March 10, 2000
Lessons learned from the mouse model of short-chain acyl-CoA dehydrogenase deficiency
P A Wood, C L Kelly-Kurtz, M E Hinsdale, et al.
Neurology
|
December 1, 1991
An atypical case of cytochrome c oxidase deficiency with biochemical heterogeneity in fibroblasts
R Lutz, A Garnica, A Shires, et al.
American Journal of Human Genetics
|
August 1, 1995
Cloning of human very-long-chain acyl-coenzyme A dehydrogenase and molecular characterization of its deficiency in two patients
T Aoyama, M Souri, I Ueno, 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 disorders
E 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 patients
S 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 disorders
W 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 oxidation
B R Powell, N G Kennaway, W J Rhead, et al.
Page
of 7
Search research articles
Search
Showing results (41-50 of 65) with videos related to
Sort By:
Page
of 7
Neurology
|
February 5, 1999
Short-chain acyl-CoA dehydrogenase deficiency: a cause of ophthalmoplegia and multicore myopathy
I Tein, R H Haslam, W J Rhead, et al.
Progress in Clinical and Biological Research
|
January 1, 1990
A murine model for short-chain acyl-CoA dehydrogenase deficiency
P A Wood, B A Amendt, W J Rhead, et al.
Pediatric Research
|
January 1, 1989
Short-chain acyl-coenzyme A dehydrogenase deficiency in mice
P A Wood, B A Amendt, W J Rhead, et al.
Advances in Experimental Medicine and Biology
|
March 10, 2000
Lessons learned from the mouse model of short-chain acyl-CoA dehydrogenase deficiency
P A Wood, C L Kelly-Kurtz, M E Hinsdale, et al.
Neurology
|
December 1, 1991
An atypical case of cytochrome c oxidase deficiency with biochemical heterogeneity in fibroblasts
R Lutz, A Garnica, A Shires, et al.
American Journal of Human Genetics
|
August 1, 1995
Cloning of human very-long-chain acyl-coenzyme A dehydrogenase and molecular characterization of its deficiency in two patients
T Aoyama, M Souri, I Ueno, 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 disorders
E 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 patients
S 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 disorders
W 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 oxidation
B R Powell, N G Kennaway, W J Rhead, et al.
Page
of 7