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D S Kerr

Showing results (61-70 of 86) with videos related to

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Pediatric Research|August 1, 1982
The newborn of diabetic rat. I. Hormonal and metabolic changes in the postnatal periodJ M Cuezva, E S Burkett, D S Kerr, et al.
Behavioural Pharmacology|March 27, 2003
AMPA/kainate and group-I metabotropic receptor antagonists infused into different brain areas impair memory formation of inhibitory avoidance in ratsJ S Bonini, L Rodrigues, D S Kerr, et al.
Spinal Cord|March 3, 2004
Client-centred assessment and the identification of meaningful treatment goals for individuals with a spinal cord injuryC Donnelly, J J Eng, J Hall, et al.
Biochimica Et Biophysica Acta|April 16, 1998
Deficiency of dihydrolipoamide dehydrogenase due to two mutant alleles (E340K and G101del). Analysis of a family and prenatal testingY S Hong, D S Kerr, T C Liu, et al.
The American Journal of Clinical Nutrition|May 1, 1983
Length of gestation and nutritional composition of human milkD M Anderson, F H Williams, R B Merkatz, et al.
Pediatric Research|August 1, 1992
A mutation in the E1 alpha subunit of pyruvate dehydrogenase associated with variable expression of pyruvate dehydrogenase complex deficiencyI D Wexler, S G Hemalatha, T C Liu, et al.
Human Molecular Genetics|December 1, 1996
Identification of two mutations in a compound heterozygous child with dihydrolipoamide dehydrogenase deficiencyY S Hong, D S Kerr, W J Craigen, et al.
Neuropharmacology|April 27, 2010
In vivo seizure induction and affinity studies of domoic acid and isodomoic acids-D, -E and -FP M Sawant, J D A Tyndall, P T Holland, et al.
Pediatric Neurology|July 1, 1989
Pyruvate carboxylase deficiency: acute exacerbation after ACTH treatment of infantile spasmsS L Rutledge, O C Snead, D R Kelly, et al.
Molecular Genetics and Metabolism|January 1, 2008
Mutations of the E1beta subunit gene (PDHB) in four families with pyruvate dehydrogenase deficiencyK Okajima, L G Korotchkina, C Prasad, et al.
Pageof 9

Showing results (61-70 of 86) with videos related to

Sort By:
Pageof 9
Pediatric Research|August 1, 1982
The newborn of diabetic rat. I. Hormonal and metabolic changes in the postnatal periodJ M Cuezva, E S Burkett, D S Kerr, et al.
Behavioural Pharmacology|March 27, 2003
AMPA/kainate and group-I metabotropic receptor antagonists infused into different brain areas impair memory formation of inhibitory avoidance in ratsJ S Bonini, L Rodrigues, D S Kerr, et al.
Spinal Cord|March 3, 2004
Client-centred assessment and the identification of meaningful treatment goals for individuals with a spinal cord injuryC Donnelly, J J Eng, J Hall, et al.
Biochimica Et Biophysica Acta|April 16, 1998
Deficiency of dihydrolipoamide dehydrogenase due to two mutant alleles (E340K and G101del). Analysis of a family and prenatal testingY S Hong, D S Kerr, T C Liu, et al.
The American Journal of Clinical Nutrition|May 1, 1983
Length of gestation and nutritional composition of human milkD M Anderson, F H Williams, R B Merkatz, et al.
Pediatric Research|August 1, 1992
A mutation in the E1 alpha subunit of pyruvate dehydrogenase associated with variable expression of pyruvate dehydrogenase complex deficiencyI D Wexler, S G Hemalatha, T C Liu, et al.
Human Molecular Genetics|December 1, 1996
Identification of two mutations in a compound heterozygous child with dihydrolipoamide dehydrogenase deficiencyY S Hong, D S Kerr, W J Craigen, et al.
Neuropharmacology|April 27, 2010
In vivo seizure induction and affinity studies of domoic acid and isodomoic acids-D, -E and -FP M Sawant, J D A Tyndall, P T Holland, et al.
Pediatric Neurology|July 1, 1989
Pyruvate carboxylase deficiency: acute exacerbation after ACTH treatment of infantile spasmsS L Rutledge, O C Snead, D R Kelly, et al.
Molecular Genetics and Metabolism|January 1, 2008
Mutations of the E1beta subunit gene (PDHB) in four families with pyruvate dehydrogenase deficiencyK Okajima, L G Korotchkina, C Prasad, et al.
Pageof 9