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Neurology
|
November 1, 1982
Adult dystonic lipidosis: clinical, histologic, and biochemical findings of a neurovisceral storage disease
W 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 disease
T D Bird, M Boehnke, J Anderson, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie
|
January 1, 1989
The genetics of Alzheimer's disease
G 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 study
T 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 dementia
T D Bird, R M Koerker, B J Leaird, et al.
Lancet (London, England)
|
February 11, 1978
Myotonic dystrophy, mitral-valve prolapse, and stroke
A 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 17q
J 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 tangles
D 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 ataxia
S R Hamilton, G E Chatrian, R P Mills, et al.
Page
of 20
Search research articles
Search
Showing results (101-110 of 194) with videos related to
Sort By:
Page
of 20
Neurology
|
November 1, 1982
Adult dystonic lipidosis: clinical, histologic, and biochemical findings of a neurovisceral storage disease
W 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 disease
T D Bird, M Boehnke, J Anderson, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie
|
January 1, 1989
The genetics of Alzheimer's disease
G 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 study
T 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 dementia
T D Bird, R M Koerker, B J Leaird, et al.
Lancet (London, England)
|
February 11, 1978
Myotonic dystrophy, mitral-valve prolapse, and stroke
A 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 17q
J 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 tangles
D 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 ataxia
S R Hamilton, G E Chatrian, R P Mills, et al.
Page
of 20