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L E Seargeant

Showing results (21-30 of 28) with videos related to

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The New England Journal of Medicine|March 15, 1984
Homocystinuria and megaloblastic anemia responsive to vitamin B12 therapy. An inborn error of metabolism due to a defect in cobalamin metabolismS Schuh, D S Rosenblatt, B A Cooper, et al.
American Journal of Medical Genetics|March 1, 1993
Symptomatic and asymptomatic methylenetetrahydrofolate reductase deficiency in two adult brothersJ C Haworth, L A Dilling, R A Surtees, et al.
The Journal of Pediatrics|October 1, 1992
Atypical features of the hepatic form of carnitine palmitoyltransferase deficiency in a Hutterite familyJ C Haworth, F Demaugre, F A Booth, et al.
The Journal of Pediatrics|July 1, 1989
Mitochondrial encephalomyopathy with associated aminoacidopathy in a male sibshipF A Booth, J C Haworth, L A Dilling, 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.
Journal of Pediatric Hematology/Oncology|October 27, 1998
Familial neuroblastoma: report of a kindred with later age at diagnosisE G Lemire, B N Chodirker, G J Williams, et al.
Human Molecular Genetics|March 1, 1995
A G-to-T transversion at the +5 position of intron 1 in the glutaryl CoA dehydrogenase gene is associated with the Island Lake variant of glutaric acidemia type IC R Greenberg, D Reimer, R Singal, et al.
Molecular Genetics and Metabolism|February 5, 2002
Outcome of the first 3-years of a DNA-based neonatal screening program for glutaric acidemia type 1 in Manitoba and northwestern Ontario, CanadaC R Greenberg, A N Prasad, L A Dilling, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
The New England Journal of Medicine|March 15, 1984
Homocystinuria and megaloblastic anemia responsive to vitamin B12 therapy. An inborn error of metabolism due to a defect in cobalamin metabolismS Schuh, D S Rosenblatt, B A Cooper, et al.
American Journal of Medical Genetics|March 1, 1993
Symptomatic and asymptomatic methylenetetrahydrofolate reductase deficiency in two adult brothersJ C Haworth, L A Dilling, R A Surtees, et al.
The Journal of Pediatrics|October 1, 1992
Atypical features of the hepatic form of carnitine palmitoyltransferase deficiency in a Hutterite familyJ C Haworth, F Demaugre, F A Booth, et al.
The Journal of Pediatrics|July 1, 1989
Mitochondrial encephalomyopathy with associated aminoacidopathy in a male sibshipF A Booth, J C Haworth, L A Dilling, 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.
Journal of Pediatric Hematology/Oncology|October 27, 1998
Familial neuroblastoma: report of a kindred with later age at diagnosisE G Lemire, B N Chodirker, G J Williams, et al.
Human Molecular Genetics|March 1, 1995
A G-to-T transversion at the +5 position of intron 1 in the glutaryl CoA dehydrogenase gene is associated with the Island Lake variant of glutaric acidemia type IC R Greenberg, D Reimer, R Singal, et al.
Molecular Genetics and Metabolism|February 5, 2002
Outcome of the first 3-years of a DNA-based neonatal screening program for glutaric acidemia type 1 in Manitoba and northwestern Ontario, CanadaC R Greenberg, A N Prasad, L A Dilling, et al.
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