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

P Rinaldo

Showing results (41-50 of 95) with videos related to

Pageof 10
Sort By:
The Journal of Pediatrics|August 1, 1997
Sudden neonatal death in carnitine transporter deficiencyP Rinaldo, C A Stanley, B Y Hsu, et al.
Pediatric Pathology|November 1, 1991
Medium-chain acyl-CoA dehydrogenase deficiency: postmortem diagnosis in a case of sudden infant death and neonatal diagnosis of an affected siblingM J Bennett, P Rinaldo, D S Millington, et al.
Neurology|July 1, 1986
Systemic carnitine deficiency due to lack of electron transfer flavoprotein:ubiquinone oxidoreductaseS Di Donato, F E Frerman, M Rimoldi, et al.
American Journal of Human Genetics|May 1, 1996
Molecular characterization of mitochondrial trifunctional protein deficiency: formation of the enzyme complex is important for stabilization of both alpha- and beta-subunitsS Ushikubo, T Aoyama, T Kamijo, et al.
Molecular Genetics and Metabolism|March 13, 2001
Placental floor infarction complicating the pregnancy of a fetus with long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiencyD Matern, B M Schehata, P Shekhawa, et al.
Molecular Genetics and Metabolism|January 27, 2005
The urinary excretion of glutarylcarnitine is an informative tool in the biochemical diagnosis of glutaric acidemia type IS Tortorelli, S H Hahn, T M Cowan, et al.
The New England Journal of Medicine|November 17, 1988
Medium-chain acyl-CoA dehydrogenase deficiency. Diagnosis by stable-isotope dilution measurement of urinary n-hexanoylglycine and 3-phenylpropionylglycineP Rinaldo, J J O'Shea, P M Coates, et al.
Neurology|November 1, 1993
Impaired fatty acid oxidation in children on valproic acid and the effect of L-carnitineB D Kossak, E Schmidt-Sommerfeld, D A Schoeller, et al.
The Journal of Pediatrics|June 1, 1995
Clinical and biochemical characterization of short-chain acyl-coenzyme A dehydrogenase deficiencyA Bhala, S M Willi, P Rinaldo, et al.
Annals of Emergency Medicine|August 25, 1999
Hypoketotic hypoglycemic coma in a 21-month-old childM A Hostetler, G L Arnold, R Mooney, et al.
Pageof 10

Showing results (41-50 of 95) with videos related to

Sort By:
Pageof 10
The Journal of Pediatrics|August 1, 1997
Sudden neonatal death in carnitine transporter deficiencyP Rinaldo, C A Stanley, B Y Hsu, et al.
Pediatric Pathology|November 1, 1991
Medium-chain acyl-CoA dehydrogenase deficiency: postmortem diagnosis in a case of sudden infant death and neonatal diagnosis of an affected siblingM J Bennett, P Rinaldo, D S Millington, et al.
Neurology|July 1, 1986
Systemic carnitine deficiency due to lack of electron transfer flavoprotein:ubiquinone oxidoreductaseS Di Donato, F E Frerman, M Rimoldi, et al.
American Journal of Human Genetics|May 1, 1996
Molecular characterization of mitochondrial trifunctional protein deficiency: formation of the enzyme complex is important for stabilization of both alpha- and beta-subunitsS Ushikubo, T Aoyama, T Kamijo, et al.
Molecular Genetics and Metabolism|March 13, 2001
Placental floor infarction complicating the pregnancy of a fetus with long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiencyD Matern, B M Schehata, P Shekhawa, et al.
Molecular Genetics and Metabolism|January 27, 2005
The urinary excretion of glutarylcarnitine is an informative tool in the biochemical diagnosis of glutaric acidemia type IS Tortorelli, S H Hahn, T M Cowan, et al.
The New England Journal of Medicine|November 17, 1988
Medium-chain acyl-CoA dehydrogenase deficiency. Diagnosis by stable-isotope dilution measurement of urinary n-hexanoylglycine and 3-phenylpropionylglycineP Rinaldo, J J O'Shea, P M Coates, et al.
Neurology|November 1, 1993
Impaired fatty acid oxidation in children on valproic acid and the effect of L-carnitineB D Kossak, E Schmidt-Sommerfeld, D A Schoeller, et al.
The Journal of Pediatrics|June 1, 1995
Clinical and biochemical characterization of short-chain acyl-coenzyme A dehydrogenase deficiencyA Bhala, S M Willi, P Rinaldo, et al.
Annals of Emergency Medicine|August 25, 1999
Hypoketotic hypoglycemic coma in a 21-month-old childM A Hostetler, G L Arnold, R Mooney, et al.
Pageof 10