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T D Bird

Showing results (101-110 of 194) with videos related to

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Neurology|November 1, 1982
Adult dystonic lipidosis: clinical, histologic, and biochemical findings of a neurovisceral storage diseaseW T Longstreth, J R Daven, D F Farrell, et al.
Archives of Neurology|September 1, 1990
Family with dominantly inherited ataxia, amyotrophy, and peripheral sensory loss. Spinopontine atrophy or Machado-Joseph Azorean disease in another non-Portuguese family?K Eto, S M Sumi, T D Bird, et al.
Alzheimer Disease and Associated Disorders|January 1, 1987
The frequency of C4B variants of complement in familial and sporadic Alzheimer diseaseT D Bird, M Boehnke, J Anderson, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|January 1, 1989
The genetics of Alzheimer's diseaseG D Schellenberg, T D Bird, E M Wijsman, et al.
Annals of Neurology|April 1, 1997
Clinical and pathological phenotype of the original family with Charcot-Marie-Tooth type 1B: a 20-year studyT D Bird, G H Kraft, H P Lipe, et al.
Neurology|January 1, 1983
Lipomembranous polycystic osteodysplasia (brain, bone, and fat disease): a genetic cause of presenile dementiaT D Bird, R M Koerker, B J Leaird, et al.
Lancet (London, England)|February 11, 1978
Myotonic dystrophy, mitral-valve prolapse, and strokeA W Cook, T D Bird, A M Spence, et al.
Neurology|April 1, 1996
Mapping of hereditary neuralgic amyotrophy (familial brachial plexus neuropathy) to distal chromosome 17qJ E Pellegrino, T R Rebbeck, M J Brown, et al.
Biological Psychiatry|January 15, 1997
The effect of apolipoprotein E genotype on expression of an autosomal dominant schizophreniform disorder with progressive dementia and neurofibrillary tanglesD Tsuang, M A Raskind, J Leverenz, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|April 1, 1990
Cone dysfunction in a subgroup of patients with autosomal dominant cerebellar ataxiaS R Hamilton, G E Chatrian, R P Mills, et al.
Pageof 20

Showing results (101-110 of 194) with videos related to

Sort By:
Pageof 20
Neurology|November 1, 1982
Adult dystonic lipidosis: clinical, histologic, and biochemical findings of a neurovisceral storage diseaseW T Longstreth, J R Daven, D F Farrell, et al.
Archives of Neurology|September 1, 1990
Family with dominantly inherited ataxia, amyotrophy, and peripheral sensory loss. Spinopontine atrophy or Machado-Joseph Azorean disease in another non-Portuguese family?K Eto, S M Sumi, T D Bird, et al.
Alzheimer Disease and Associated Disorders|January 1, 1987
The frequency of C4B variants of complement in familial and sporadic Alzheimer diseaseT D Bird, M Boehnke, J Anderson, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|January 1, 1989
The genetics of Alzheimer's diseaseG D Schellenberg, T D Bird, E M Wijsman, et al.
Annals of Neurology|April 1, 1997
Clinical and pathological phenotype of the original family with Charcot-Marie-Tooth type 1B: a 20-year studyT D Bird, G H Kraft, H P Lipe, et al.
Neurology|January 1, 1983
Lipomembranous polycystic osteodysplasia (brain, bone, and fat disease): a genetic cause of presenile dementiaT D Bird, R M Koerker, B J Leaird, et al.
Lancet (London, England)|February 11, 1978
Myotonic dystrophy, mitral-valve prolapse, and strokeA W Cook, T D Bird, A M Spence, et al.
Neurology|April 1, 1996
Mapping of hereditary neuralgic amyotrophy (familial brachial plexus neuropathy) to distal chromosome 17qJ E Pellegrino, T R Rebbeck, M J Brown, et al.
Biological Psychiatry|January 15, 1997
The effect of apolipoprotein E genotype on expression of an autosomal dominant schizophreniform disorder with progressive dementia and neurofibrillary tanglesD Tsuang, M A Raskind, J Leverenz, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|April 1, 1990
Cone dysfunction in a subgroup of patients with autosomal dominant cerebellar ataxiaS R Hamilton, G E Chatrian, R P Mills, et al.
Pageof 20