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T D Bird

Showing results (131-140 of 194) with videos related to

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American Journal of Medical Genetics. Part A|July 22, 2004
parkin mutation analysis in clinic patients with early-onset Parkinson [corrected] diseaseP Poorkaj, J G Nutt, D James, et al.
Annals of Neurology|May 1, 1994
Hereditary motor and sensory neuropathy with diaphragm and vocal cord paresisP J Dyck, W J Litchy, S Minnerath, et al.
Experimental Gerontology|November 1, 1994
Trypsin inhibitor activities of fibroblasts increase with age of donor and are unaltered in familial Alzheimer's diseaseM G Hearn, S D Edland, C E Ogburn, et al.
Progress in Clinical and Biological Research|January 1, 1989
Characteristics of familial Alzheimer's disease in nine kindreds of Volga German ancestryT D Bird, T H Lampe, E J Nemens, et al.
American Journal of Human Genetics|January 1, 1992
Multicolor in situ hybridization and linkage analysis order Charcot-Marie-Tooth type I (CMTIA) gene-region markersR V Lebo, E D Lynch, T D Bird, et al.
Neurobiology of Aging|March 1, 1993
Intracellular calcium response is reduced in CD4+ lymphocytes in Alzheimer's disease and in older persons with Down's syndromeA Grossmann, W A Kukull, J C Jinneman, et al.
Journal of Neurogenetics|April 1, 1987
Association of an apolipoprotein CII allele with familial dementia of the Alzheimer typeG D Schellenberg, S S Deeb, M Boehnke, et al.
Annals of Neurology|December 1, 1996
Wide range in age of onset for chromosome 1--related familial Alzheimer's diseaseT D Bird, E Levy-Lahad, P Poorkaj, et al.
JAMA|May 4, 1994
Alzheimer's disease, apolipoprotein E4, and genderH Payami, K R Montee, J A Kaye, et al.
Neuromuscular Disorders : NMD|September 5, 2002
Charcot-Marie-Tooth neuropathy: clinical phenotypes of four novel mutations in the MPZ and Cx 32 genesV A Street, G Meekins, H P Lipe, et al.
Pageof 20

Showing results (131-140 of 194) with videos related to

Sort By:
Pageof 20
American Journal of Medical Genetics. Part A|July 22, 2004
parkin mutation analysis in clinic patients with early-onset Parkinson [corrected] diseaseP Poorkaj, J G Nutt, D James, et al.
Annals of Neurology|May 1, 1994
Hereditary motor and sensory neuropathy with diaphragm and vocal cord paresisP J Dyck, W J Litchy, S Minnerath, et al.
Experimental Gerontology|November 1, 1994
Trypsin inhibitor activities of fibroblasts increase with age of donor and are unaltered in familial Alzheimer's diseaseM G Hearn, S D Edland, C E Ogburn, et al.
Progress in Clinical and Biological Research|January 1, 1989
Characteristics of familial Alzheimer's disease in nine kindreds of Volga German ancestryT D Bird, T H Lampe, E J Nemens, et al.
American Journal of Human Genetics|January 1, 1992
Multicolor in situ hybridization and linkage analysis order Charcot-Marie-Tooth type I (CMTIA) gene-region markersR V Lebo, E D Lynch, T D Bird, et al.
Neurobiology of Aging|March 1, 1993
Intracellular calcium response is reduced in CD4+ lymphocytes in Alzheimer's disease and in older persons with Down's syndromeA Grossmann, W A Kukull, J C Jinneman, et al.
Journal of Neurogenetics|April 1, 1987
Association of an apolipoprotein CII allele with familial dementia of the Alzheimer typeG D Schellenberg, S S Deeb, M Boehnke, et al.
Annals of Neurology|December 1, 1996
Wide range in age of onset for chromosome 1--related familial Alzheimer's diseaseT D Bird, E Levy-Lahad, P Poorkaj, et al.
JAMA|May 4, 1994
Alzheimer's disease, apolipoprotein E4, and genderH Payami, K R Montee, J A Kaye, et al.
Neuromuscular Disorders : NMD|September 5, 2002
Charcot-Marie-Tooth neuropathy: clinical phenotypes of four novel mutations in the MPZ and Cx 32 genesV A Street, G Meekins, H P Lipe, et al.
Pageof 20