Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

F E Frerman

Showing results (71-80 of 80) with videos related to

Pageof 8
Sort By:
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 IIC 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 oxidoreductaseS 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 coliS 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 hypoglycemiaD 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 geneD 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 III 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 deficiencyM 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 changesC A Chisholm, F Vavelidis, M A Lovell, et al.
Neurology|November 1, 1990
Electron transfer flavoprotein: ubiquinone oxidoreductase (ETF:QO) deficiency in an adultR 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 oxidationR S Kler, S Jackson, K Bartlett, et al.
Pageof 8

Showing results (71-80 of 80) with videos related to

Sort By:
Pageof 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 IIC 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 oxidoreductaseS 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 coliS 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 hypoglycemiaD 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 geneD 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 III 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 deficiencyM 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 changesC A Chisholm, F Vavelidis, M A Lovell, et al.
Neurology|November 1, 1990
Electron transfer flavoprotein: ubiquinone oxidoreductase (ETF:QO) deficiency in an adultR 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 oxidationR S Kler, S Jackson, K Bartlett, et al.
Pageof 8