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D E HALE

Showing results (71-80 of 85) with videos related to

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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.
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.
Lancet (London, England)|February 21, 1987
Prenatal diagnosis of medium-chain acyl-CoA dehydrogenase deficiency in family with sudden infant deathM J Bennett, F Allison, R J Pollitt, et al.
Lancet (London, England)|December 14, 1991
New clinical phenotype of branched-chain acyl-CoA oxidation defectA Burlina, F Zacchello, C Dionisi-Vici, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Analysis of abnormal urinary metabolites in the newborn period in medium-chain acyl-CoA dehydrogenase deficiencyM J Bennett, P M Coates, D E Hale, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 31, 1995
The molecular basis of pediatric long chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with maternal acute fatty liver of pregnancyH F Sims, J C Brackett, C K Powell, et al.
The American Journal of Gastroenterology|November 1, 1996
Acute fatty liver of pregnancy, hemolysis, elevated liver enzymes, and low platelets syndrome, and long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiencyW R Treem, M E Shoup, D E Hale, et al.
The Journal of Pediatrics|January 1, 1994
A new syndrome with ethylmalonic aciduria and normal fatty acid oxidation in fibroblastsA B Burlina, C Dionisi-Vici, M J Bennett, et al.
American Journal of Medical Genetics|March 3, 1997
Growth hormone deficiency associated in the 18q deletion syndromeP D Ghidoni, D E Hale, J D Cody, et al.
Pediatric Research|November 1, 1983
Medium-chain acyl-CoA dehydrogenase deficiency in children with non-ketotic hypoglycemia and low carnitine levelsC A Stanley, D E Hale, P M Coates, et al.
Pageof 9

Showing results (71-80 of 85) with videos related to

Sort By:
Pageof 9
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.
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.
Lancet (London, England)|February 21, 1987
Prenatal diagnosis of medium-chain acyl-CoA dehydrogenase deficiency in family with sudden infant deathM J Bennett, F Allison, R J Pollitt, et al.
Lancet (London, England)|December 14, 1991
New clinical phenotype of branched-chain acyl-CoA oxidation defectA Burlina, F Zacchello, C Dionisi-Vici, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Analysis of abnormal urinary metabolites in the newborn period in medium-chain acyl-CoA dehydrogenase deficiencyM J Bennett, P M Coates, D E Hale, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 31, 1995
The molecular basis of pediatric long chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with maternal acute fatty liver of pregnancyH F Sims, J C Brackett, C K Powell, et al.
The American Journal of Gastroenterology|November 1, 1996
Acute fatty liver of pregnancy, hemolysis, elevated liver enzymes, and low platelets syndrome, and long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiencyW R Treem, M E Shoup, D E Hale, et al.
The Journal of Pediatrics|January 1, 1994
A new syndrome with ethylmalonic aciduria and normal fatty acid oxidation in fibroblastsA B Burlina, C Dionisi-Vici, M J Bennett, et al.
American Journal of Medical Genetics|March 3, 1997
Growth hormone deficiency associated in the 18q deletion syndromeP D Ghidoni, D E Hale, J D Cody, et al.
Pediatric Research|November 1, 1983
Medium-chain acyl-CoA dehydrogenase deficiency in children with non-ketotic hypoglycemia and low carnitine levelsC A Stanley, D E Hale, P M Coates, et al.
Pageof 9