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Acta Neuropathologica
|
January 1, 1989
Striatal degeneration in glutaric acidaemia type II
C W Chow, F E Frerman, S I Goodman, et al.
European Journal of Biochemistry
|
January 15, 1994
Molecular cloning and expression of a cDNA encoding human electron transfer flavoprotein-ubiquinone oxidoreductase
S I Goodman, K M Axtell, L A Bindoff, et al.
Human Molecular Genetics
|
September 1, 1995
Cloning of glutaryl-CoA dehydrogenase cDNA, and expression of wild type and mutant enzymes in Escherichia coli
S I Goodman, L E Kratz, K A DiGiulio, et al.
Pediatric Research
|
July 1, 1985
Long-chain acyl coenzyme A dehydrogenase deficiency: an inherited cause of nonketotic hypoglycemia
D E Hale, M L Batshaw, P M Coates, et al.
Genomics
|
August 10, 1995
Cloning, structure, and chromosome localization of the mouse glutaryl-CoA dehydrogenase gene
D M Koeller, K A DiGiulio, S V Angeloni, et al.
Progress in Clinical and Biological Research
|
January 1, 1992
Molecular heterogeneity of beta-ETF deficiency in glutaric aciduria type II
I Colombo, S DiDonato, M Volta, et al.
Pediatric Pathology
|
January 1, 1990
Glutaric aciduria type II: autopsy study of a case with electron-transferring flavoprotein dehydrogenase deficiency
M Kamiya, T Eimoto, H Kishimoto, et al.
Prenatal Diagnosis
|
December 18, 2001
Prenatal diagnosis of multiple acyl-CoA dehydrogenase deficiency: association with elevated alpha-fetoprotein and cystic renal changes
C A Chisholm, F Vavelidis, M A Lovell, et al.
Neurology
|
November 1, 1990
Electron transfer flavoprotein: ubiquinone oxidoreductase (ETF:QO) deficiency in an adult
R B Bell, A K Brownell, C R Roe, et al.
The Journal of Biological Chemistry
|
December 5, 1991
Quantitation of acyl-CoA and acylcarnitine esters accumulated during abnormal mitochondrial fatty acid oxidation
R S Kler, S Jackson, K Bartlett, et al.
Page
of 8
Search research articles
Search
Showing results (71-80 of 80) with videos related to
Sort By:
Page
of 8
You have reached the last page of results.
This site can display upto 80 results.
Acta Neuropathologica
|
January 1, 1989
Striatal degeneration in glutaric acidaemia type II
C W Chow, F E Frerman, S I Goodman, et al.
European Journal of Biochemistry
|
January 15, 1994
Molecular cloning and expression of a cDNA encoding human electron transfer flavoprotein-ubiquinone oxidoreductase
S I Goodman, K M Axtell, L A Bindoff, et al.
Human Molecular Genetics
|
September 1, 1995
Cloning of glutaryl-CoA dehydrogenase cDNA, and expression of wild type and mutant enzymes in Escherichia coli
S I Goodman, L E Kratz, K A DiGiulio, et al.
Pediatric Research
|
July 1, 1985
Long-chain acyl coenzyme A dehydrogenase deficiency: an inherited cause of nonketotic hypoglycemia
D E Hale, M L Batshaw, P M Coates, et al.
Genomics
|
August 10, 1995
Cloning, structure, and chromosome localization of the mouse glutaryl-CoA dehydrogenase gene
D M Koeller, K A DiGiulio, S V Angeloni, et al.
Progress in Clinical and Biological Research
|
January 1, 1992
Molecular heterogeneity of beta-ETF deficiency in glutaric aciduria type II
I Colombo, S DiDonato, M Volta, et al.
Pediatric Pathology
|
January 1, 1990
Glutaric aciduria type II: autopsy study of a case with electron-transferring flavoprotein dehydrogenase deficiency
M Kamiya, T Eimoto, H Kishimoto, et al.
Prenatal Diagnosis
|
December 18, 2001
Prenatal diagnosis of multiple acyl-CoA dehydrogenase deficiency: association with elevated alpha-fetoprotein and cystic renal changes
C A Chisholm, F Vavelidis, M A Lovell, et al.
Neurology
|
November 1, 1990
Electron transfer flavoprotein: ubiquinone oxidoreductase (ETF:QO) deficiency in an adult
R B Bell, A K Brownell, C R Roe, et al.
The Journal of Biological Chemistry
|
December 5, 1991
Quantitation of acyl-CoA and acylcarnitine esters accumulated during abnormal mitochondrial fatty acid oxidation
R S Kler, S Jackson, K Bartlett, et al.
Page
of 8