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C A Stanley

Showing results (81-90 of 106) with videos related to

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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.
The Journal of Clinical Investigation|July 1, 1990
Impaired metabolic function and signaling defects in phagocytic cells in glycogen storage disease type 1bL Kilpatrick, B Z Garty, K F Lundquist, et al.
Hepatology (Baltimore, Md.)|November 1, 1986
Medium-chain and long-chain acyl CoA dehydrogenase deficiency: clinical, pathologic and ultrastructural differentiation from Reye's syndromeW R Treem, C A Witzleben, D A Piccoli, et al.
The Journal of Pediatrics|August 1, 1997
Insulin-like growth factor binding protein-1 levels in the diagnosis of hypoglycemia caused by hyperinsulinismL E Levitt Katz, M S Satin-Smith, P Collett-Solberg, et al.
Hepatology (Baltimore, Md.)|February 1, 1994
Acute fatty liver of pregnancy and long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiencyW R Treem, P Rinaldo, D E Hale, et al.
Molecular Genetics and Metabolism|October 11, 2001
Aberrant mRNA splicing associated with coding region mutations in children with carnitine-acylcarnitine translocase deficiencyB Y Hsu, V Iacobazzi, Z Wang, et al.
Pediatric Research|January 1, 1994
In vitro and in vivo effects of granulocyte colony-stimulating factor on neutrophils in glycogen storage disease type 1B: granulocyte colony-stimulating factor therapy corrects the neutropenia and the defects in respiratory burst activity and Ca2+ mobilizationL J McCawley, H M Korchak, S D Douglas, et al.
Human Molecular Genetics|June 9, 1998
Genetic heterogeneity in familial hyperinsulinismA Nestorowicz, B Glaser, B A Wilson, et al.
American Journal of Medical Genetics|December 2, 1996
First prenatal diagnosis of the carnitine transporter defectJ Christodoulou, S H Teo, J Hammond, et al.
The Journal of Clinical Endocrinology and Metabolism|January 1, 2013
Genotype and phenotype correlations in 417 children with congenital hyperinsulinismK E Snider, S Becker, L Boyajian, et al.
Pageof 11

Showing results (81-90 of 106) with videos related to

Sort By:
Pageof 11
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.
The Journal of Clinical Investigation|July 1, 1990
Impaired metabolic function and signaling defects in phagocytic cells in glycogen storage disease type 1bL Kilpatrick, B Z Garty, K F Lundquist, et al.
Hepatology (Baltimore, Md.)|November 1, 1986
Medium-chain and long-chain acyl CoA dehydrogenase deficiency: clinical, pathologic and ultrastructural differentiation from Reye's syndromeW R Treem, C A Witzleben, D A Piccoli, et al.
The Journal of Pediatrics|August 1, 1997
Insulin-like growth factor binding protein-1 levels in the diagnosis of hypoglycemia caused by hyperinsulinismL E Levitt Katz, M S Satin-Smith, P Collett-Solberg, et al.
Hepatology (Baltimore, Md.)|February 1, 1994
Acute fatty liver of pregnancy and long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiencyW R Treem, P Rinaldo, D E Hale, et al.
Molecular Genetics and Metabolism|October 11, 2001
Aberrant mRNA splicing associated with coding region mutations in children with carnitine-acylcarnitine translocase deficiencyB Y Hsu, V Iacobazzi, Z Wang, et al.
Pediatric Research|January 1, 1994
In vitro and in vivo effects of granulocyte colony-stimulating factor on neutrophils in glycogen storage disease type 1B: granulocyte colony-stimulating factor therapy corrects the neutropenia and the defects in respiratory burst activity and Ca2+ mobilizationL J McCawley, H M Korchak, S D Douglas, et al.
Human Molecular Genetics|June 9, 1998
Genetic heterogeneity in familial hyperinsulinismA Nestorowicz, B Glaser, B A Wilson, et al.
American Journal of Medical Genetics|December 2, 1996
First prenatal diagnosis of the carnitine transporter defectJ Christodoulou, S H Teo, J Hammond, et al.
The Journal of Clinical Endocrinology and Metabolism|January 1, 2013
Genotype and phenotype correlations in 417 children with congenital hyperinsulinismK E Snider, S Becker, L Boyajian, et al.
Pageof 11