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T D Bird

Showing results (161-170 of 194) with videos related to

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Neurology|May 29, 2001
Parkinson's disease, CYP2D6 polymorphism, and ageH Payami, N Lee, S Zareparsi, et al.
Science (New York, N.Y.)|October 23, 1992
Genetic linkage evidence for a familial Alzheimer's disease locus on chromosome 14G D Schellenberg, T D Bird, E M Wijsman, et al.
Human Genetics|January 24, 1998
Hereditary neuralgic amyotrophy: evidence for genetic homogeneity and mapping to chromosome 17q25J E Pellegrino, R A George, J Biegel, et al.
Cell|January 15, 1993
DNA deletion associated with hereditary neuropathy with liability to pressure palsiesP F Chance, M K Alderson, K A Leppig, et al.
Annals of Neurology|August 12, 1999
Ataxin 1 and ataxin 3 in neuronal intranuclear inclusion diseaseA P Lieberman, J Q Trojanowski, D G Leonard, et al.
Science (New York, N.Y.)|September 16, 1988
Absence of linkage of chromosome 21q21 markers to familial Alzheimer's diseaseG D Schellenberg, T D Bird, E M Wijsman, et al.
Neurology|March 1, 1990
Transmission and age-at-onset patterns in familial Alzheimer's disease: evidence for heterogeneityL A Farrer, R H Myers, L A Cupples, et al.
Annals of Neurology|September 8, 2000
Familial Alzheimer's disease: site of mutation influences clinical phenotypeC F Lippa, J M Swearer, K J Kane, et al.
Brain : a Journal of Neurology|April 19, 2007
A novel progranulin mutation associated with variable clinical presentation and tau, TDP43 and alpha-synuclein pathologyJ B Leverenz, C E Yu, T J Montine, et al.
Neurology|January 15, 2003
Mutation of a putative protein degradation gene LITAF/SIMPLE in Charcot-Marie-Tooth disease 1CV A Street, C L Bennett, J D Goldy, et al.
Pageof 20

Showing results (161-170 of 194) with videos related to

Sort By:
Pageof 20
Neurology|May 29, 2001
Parkinson's disease, CYP2D6 polymorphism, and ageH Payami, N Lee, S Zareparsi, et al.
Science (New York, N.Y.)|October 23, 1992
Genetic linkage evidence for a familial Alzheimer's disease locus on chromosome 14G D Schellenberg, T D Bird, E M Wijsman, et al.
Human Genetics|January 24, 1998
Hereditary neuralgic amyotrophy: evidence for genetic homogeneity and mapping to chromosome 17q25J E Pellegrino, R A George, J Biegel, et al.
Cell|January 15, 1993
DNA deletion associated with hereditary neuropathy with liability to pressure palsiesP F Chance, M K Alderson, K A Leppig, et al.
Annals of Neurology|August 12, 1999
Ataxin 1 and ataxin 3 in neuronal intranuclear inclusion diseaseA P Lieberman, J Q Trojanowski, D G Leonard, et al.
Science (New York, N.Y.)|September 16, 1988
Absence of linkage of chromosome 21q21 markers to familial Alzheimer's diseaseG D Schellenberg, T D Bird, E M Wijsman, et al.
Neurology|March 1, 1990
Transmission and age-at-onset patterns in familial Alzheimer's disease: evidence for heterogeneityL A Farrer, R H Myers, L A Cupples, et al.
Annals of Neurology|September 8, 2000
Familial Alzheimer's disease: site of mutation influences clinical phenotypeC F Lippa, J M Swearer, K J Kane, et al.
Brain : a Journal of Neurology|April 19, 2007
A novel progranulin mutation associated with variable clinical presentation and tau, TDP43 and alpha-synuclein pathologyJ B Leverenz, C E Yu, T J Montine, et al.
Neurology|January 15, 2003
Mutation of a putative protein degradation gene LITAF/SIMPLE in Charcot-Marie-Tooth disease 1CV A Street, C L Bennett, J D Goldy, et al.
Pageof 20