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T D Bird

Showing results (81-90 of 194) with videos related to

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Annals of Neurology|March 1, 1978
Familial degeneration of the basal ganglia with acanthocytosis: a clinical, neuropathological, and neurochemical studyT D Bird, S Cederbaum, R W Valey, et al.
Archives of Neurology|November 16, 2001
Impact of DNA testing for early-onset familial Alzheimer disease and frontotemporal dementiaE J Steinbart, C O Smith, P Poorkaj, et al.
Journal of Medical Genetics|August 1, 1985
Hereditary sideroblastic anaemia and ataxia: an X linked recessive disorderR A Pagon, T D Bird, J C Detter, et al.
Gastroenterology|November 1, 1978
A familial neuronal disease presenting as intestinal pseudoobstructionM D Schuffler, T D Bird, S M Sumi, et al.
Neurology|December 12, 2001
Craniofacial and cutaneous findings expand the phenotype of hereditary neuralgic amyotrophyP Y Jeannet, G D Watts, T D Bird, et al.
Journal of the Neurological Sciences|November 1, 1984
Effects of L-glutamate on viabilities of cultured diploid skin fibroblasts and lymphocytes. Increased toxicity not observed in Huntington's diseaseW L Stahl, C B Ward, J B Casper, et al.
American Journal of Human Genetics|December 1, 1991
Complete deletion of the proteolipid protein gene (PLP) in a family with X-linked Pelizaeus-Merzbacher diseaseW H Raskind, C A Williams, L D Hudson, et al.
Neurology|October 1, 1992
Analysis of the DNA duplication 17p11.2 in Charcot-Marie-Tooth neuropathy type 1 pedigrees: additional evidence for a third autosomal CMT1 locusP F Chance, N Matsunami, W Lensch, et al.
Neurology|February 1, 1987
Genetic linkage relationships of Charcot-Marie-Tooth disease (HMSN-Ib) to chromosome 1 markersP F Chance, J C Murray, T D Bird, et al.
Nature Genetics|August 1, 1997
Trinucleotide repeat expansion at the myotonic dystrophy locus reduces expression of DMAHPT R Klesert, A D Otten, T D Bird, et al.
Pageof 20

Showing results (81-90 of 194) with videos related to

Sort By:
Pageof 20
Annals of Neurology|March 1, 1978
Familial degeneration of the basal ganglia with acanthocytosis: a clinical, neuropathological, and neurochemical studyT D Bird, S Cederbaum, R W Valey, et al.
Archives of Neurology|November 16, 2001
Impact of DNA testing for early-onset familial Alzheimer disease and frontotemporal dementiaE J Steinbart, C O Smith, P Poorkaj, et al.
Journal of Medical Genetics|August 1, 1985
Hereditary sideroblastic anaemia and ataxia: an X linked recessive disorderR A Pagon, T D Bird, J C Detter, et al.
Gastroenterology|November 1, 1978
A familial neuronal disease presenting as intestinal pseudoobstructionM D Schuffler, T D Bird, S M Sumi, et al.
Neurology|December 12, 2001
Craniofacial and cutaneous findings expand the phenotype of hereditary neuralgic amyotrophyP Y Jeannet, G D Watts, T D Bird, et al.
Journal of the Neurological Sciences|November 1, 1984
Effects of L-glutamate on viabilities of cultured diploid skin fibroblasts and lymphocytes. Increased toxicity not observed in Huntington's diseaseW L Stahl, C B Ward, J B Casper, et al.
American Journal of Human Genetics|December 1, 1991
Complete deletion of the proteolipid protein gene (PLP) in a family with X-linked Pelizaeus-Merzbacher diseaseW H Raskind, C A Williams, L D Hudson, et al.
Neurology|October 1, 1992
Analysis of the DNA duplication 17p11.2 in Charcot-Marie-Tooth neuropathy type 1 pedigrees: additional evidence for a third autosomal CMT1 locusP F Chance, N Matsunami, W Lensch, et al.
Neurology|February 1, 1987
Genetic linkage relationships of Charcot-Marie-Tooth disease (HMSN-Ib) to chromosome 1 markersP F Chance, J C Murray, T D Bird, et al.
Nature Genetics|August 1, 1997
Trinucleotide repeat expansion at the myotonic dystrophy locus reduces expression of DMAHPT R Klesert, A D Otten, T D Bird, et al.
Pageof 20