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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 patients
B 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 riboflavin
W J Triggs, C R Roe, W J Rhead, et al.
Nature Genetics
|
November 1, 1996
Mutations in the glutathione synthetase gene cause 5-oxoprolinuria
Z 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 dehydrogenase
T 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 patients
T 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 deficiencies
C 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 sibship
F 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 patient
J 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 deficiency
Y 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 finding
W B Hanley, L D Platt, R P Bachman, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 65) with videos related to
Sort By:
Page
of 7
The Journal of Clinical Investigation
|
May 1, 1987
Short-chain acyl-coenzyme A dehydrogenase deficiency. Clinical and biochemical studies in two patients
B 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 riboflavin
W J Triggs, C R Roe, W J Rhead, et al.
Nature Genetics
|
November 1, 1996
Mutations in the glutathione synthetase gene cause 5-oxoprolinuria
Z 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 dehydrogenase
T 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 patients
T 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 deficiencies
C 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 sibship
F 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 patient
J 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 deficiency
Y 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 finding
W B Hanley, L D Platt, R P Bachman, et al.
Page
of 7