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

C R Roe

Showing results (111-120 of 122) with videos related to

Pageof 13
Sort By:
Molecular Genetics and Metabolism|May 15, 2001
Carnitine/acylcarnitine translocase deficiency (neonatal phenotype): successful prenatal and postmortem diagnosis associated with a novel mutation in a single familyB Z Yang, J M Mallory, D S Roe, et al.
The Journal of Pediatrics|August 1, 1989
Parenteral nutrition in propionic and methylmalonic acidemiaS G Kahler, D S Millington, S D Cederbaum, et al.
The Journal of Thoracic and Cardiovascular Surgery|September 1, 1977
The safety of induced ventricular fibrillation during cardiopulmonary bypass in nonhypertrophied heartsJ L Cox, R W Anderson, H I Pass, 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.
Circulation|June 1, 1974
Coronary perfusion versus cold ischemic arrest during aortic valve surgery. A randomized studyR N Sapsford, E H Blackstone, J W Kirklin, et al.
Biochemical and Biophysical Research Communications|August 31, 1990
Identification of a common mutation in patients with medium-chain acyl-CoA dehydrogenase deficiencyY Matsubara, K Narisawa, S Miyabayashi, et al.
Pediatric Research|January 7, 2000
Hepatic carnitine palmitoyltransferase I deficiency presenting as maternal illness in pregnancyA M Innes, L E Seargeant, K Balachandra, et al.
Cancer Research|October 15, 1992
The effect of an amino acid-lowering diet on the rate of melphalan entry into brain and xenotransplanted gliomaD R Groothuis, B E Lippitz, I Fekete, et al.
Prenatal Diagnosis|February 1, 1996
Prenatal diagnosis of mitochondrial fatty acid oxidation defectsM A Nada, C Vianey-Saban, C R Roe, et al.
American Journal of Human Genetics|May 1, 1993
Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: diagnosis by acylcarnitine analysis in bloodJ L Van Hove, W Zhang, S G Kahler, et al.
Pageof 13

Showing results (111-120 of 122) with videos related to

Sort By:
Pageof 13
Molecular Genetics and Metabolism|May 15, 2001
Carnitine/acylcarnitine translocase deficiency (neonatal phenotype): successful prenatal and postmortem diagnosis associated with a novel mutation in a single familyB Z Yang, J M Mallory, D S Roe, et al.
The Journal of Pediatrics|August 1, 1989
Parenteral nutrition in propionic and methylmalonic acidemiaS G Kahler, D S Millington, S D Cederbaum, et al.
The Journal of Thoracic and Cardiovascular Surgery|September 1, 1977
The safety of induced ventricular fibrillation during cardiopulmonary bypass in nonhypertrophied heartsJ L Cox, R W Anderson, H I Pass, 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.
Circulation|June 1, 1974
Coronary perfusion versus cold ischemic arrest during aortic valve surgery. A randomized studyR N Sapsford, E H Blackstone, J W Kirklin, et al.
Biochemical and Biophysical Research Communications|August 31, 1990
Identification of a common mutation in patients with medium-chain acyl-CoA dehydrogenase deficiencyY Matsubara, K Narisawa, S Miyabayashi, et al.
Pediatric Research|January 7, 2000
Hepatic carnitine palmitoyltransferase I deficiency presenting as maternal illness in pregnancyA M Innes, L E Seargeant, K Balachandra, et al.
Cancer Research|October 15, 1992
The effect of an amino acid-lowering diet on the rate of melphalan entry into brain and xenotransplanted gliomaD R Groothuis, B E Lippitz, I Fekete, et al.
Prenatal Diagnosis|February 1, 1996
Prenatal diagnosis of mitochondrial fatty acid oxidation defectsM A Nada, C Vianey-Saban, C R Roe, et al.
American Journal of Human Genetics|May 1, 1993
Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: diagnosis by acylcarnitine analysis in bloodJ L Van Hove, W Zhang, S G Kahler, et al.
Pageof 13