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 A Stanley

Showing results (71-80 of 106) with videos related to

Pageof 11
Sort By:
Pediatric Research|May 1, 1986
Impaired chemotaxis and neutrophil (polymorphonuclear leukocyte) function in glycogenosis type IBN L Koven, M M Clark, C S Cody, et al.
Pediatric Research|July 1, 1993
Renal handling of carnitine in secondary carnitine deficiency disordersC A Stanley, G T Berry, M J Bennett, et al.
The Journal of Clinical Endocrinology and Metabolism|August 15, 2001
Acute insulin responses to leucine in children with the hyperinsulinism/hyperammonemia syndromeA Kelly, D Ng, R J Ferry, et al.
Clinical Genetics|May 23, 2006
The personal experience of juvenile Huntington's disease: an interpretative phenomenological analysis of parents' accounts of the primary features of a rare genetic conditionJ A Smith, H M Brewer, V Eatough, et al.
Recent Progress in Hormone Research|October 14, 1998
Genetics of type II diabetesM A Permutt, K Chiu, J Ferrer, et al.
Pediatric Research|September 1, 1993
Interferon-gamma corrects the respiratory burst defect in vitro in monocyte-derived macrophages from glycogen storage disease type 1b patientsL J McCawley, H M Korchak, J R Cutilli, et al.
Kidney International|June 1, 1989
Hyperfiltration and renal disease in glycogen storage disease, type IL Baker, S Dahlem, S Goldfarb, et al.
Diabetes|July 30, 1999
Hyperinsulinism caused by paternal-specific inheritance of a recessive mutation in the sulfonylurea-receptor geneB Glaser, F Ryan, M Donath, et al.
The Journal of Clinical Investigation|September 1, 1988
Relationship between unusual hepatic acyl coenzyme A profiles and the pathogenesis of Reye syndromeB E Corkey, D E Hale, M C Glennon, et al.
The Journal of Pediatrics|October 1, 1981
Dietary-dependent carnitine deficiency as a cause of nonketotic hypoglycemia in an infantA E Slonim, P R Borum, K Tanaka, et al.
Pageof 11

Showing results (71-80 of 106) with videos related to

Sort By:
Pageof 11
Pediatric Research|May 1, 1986
Impaired chemotaxis and neutrophil (polymorphonuclear leukocyte) function in glycogenosis type IBN L Koven, M M Clark, C S Cody, et al.
Pediatric Research|July 1, 1993
Renal handling of carnitine in secondary carnitine deficiency disordersC A Stanley, G T Berry, M J Bennett, et al.
The Journal of Clinical Endocrinology and Metabolism|August 15, 2001
Acute insulin responses to leucine in children with the hyperinsulinism/hyperammonemia syndromeA Kelly, D Ng, R J Ferry, et al.
Clinical Genetics|May 23, 2006
The personal experience of juvenile Huntington's disease: an interpretative phenomenological analysis of parents' accounts of the primary features of a rare genetic conditionJ A Smith, H M Brewer, V Eatough, et al.
Recent Progress in Hormone Research|October 14, 1998
Genetics of type II diabetesM A Permutt, K Chiu, J Ferrer, et al.
Pediatric Research|September 1, 1993
Interferon-gamma corrects the respiratory burst defect in vitro in monocyte-derived macrophages from glycogen storage disease type 1b patientsL J McCawley, H M Korchak, J R Cutilli, et al.
Kidney International|June 1, 1989
Hyperfiltration and renal disease in glycogen storage disease, type IL Baker, S Dahlem, S Goldfarb, et al.
Diabetes|July 30, 1999
Hyperinsulinism caused by paternal-specific inheritance of a recessive mutation in the sulfonylurea-receptor geneB Glaser, F Ryan, M Donath, et al.
The Journal of Clinical Investigation|September 1, 1988
Relationship between unusual hepatic acyl coenzyme A profiles and the pathogenesis of Reye syndromeB E Corkey, D E Hale, M C Glennon, et al.
The Journal of Pediatrics|October 1, 1981
Dietary-dependent carnitine deficiency as a cause of nonketotic hypoglycemia in an infantA E Slonim, P R Borum, K Tanaka, et al.
Pageof 11