Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

T D Bird

Showing results (171-180 of 194) with videos related to

Pageof 20
Sort By:
Archives of Neurology|March 20, 2001
Frequency of tau gene mutations in familial and sporadic cases of non-Alzheimer dementiaP Poorkaj, M Grossman, E Steinbart, et al.
Human Genetics|November 1, 1991
Chromosome 1 Charcot-Marie-Tooth disease (CMT1B) locus in the Fc gamma receptor gene regionR V Lebo, P F Chance, P J Dyck, et al.
American Journal of Human Genetics|April 1, 1996
Gender difference in apolipoprotein E-associated risk for familial Alzheimer disease: a possible clue to the higher incidence of Alzheimer disease in womenH Payami, S Zareparsi, K R Montee, et al.
Neurology|December 17, 1998
Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia familiesM L Moseley, K A Benzow, L J Schut, et al.
Neurology|May 23, 2008
Late-onset hereditary axonal neuropathiesC L Bennett, V H Lawson, K L Brickell, et al.
Brain : a Journal of Neurology|September 1, 1999
The impact of different presenilin 1 andpresenilin 2 mutations on amyloid deposition, neurofibrillary changes and neuronal loss in the familial Alzheimer's disease brain: evidence for other phenotype-modifying factorsT Gómez-Isla, W B Growdon, M J McNamara, et al.
Annals of Neurology|June 1, 1997
Presenilin-1 protein expression in familial and sporadic Alzheimer's diseaseA I Levey, C J Heilman, J J Lah, et al.
Genes, Brain, and Behavior|October 19, 2017
Variants regulating ZBTB4 are associated with age-at-onset of Alzheimer's diseaseE E Blue, C-E Yu, T A Thornton, et al.
Neurology|May 5, 1998
Gender-related penetrance and de novo GTP-cyclohydrolase I gene mutations in dopa-responsive dystoniaY Furukawa, A E Lang, J M Trugman, et al.
Annals of Neurology|August 1, 1996
Amyloid beta protein (Abeta) deposition in chromosome 14-linked Alzheimer's disease: predominance of Abeta42(43)D M Mann, T Iwatsubo, N J Cairns, et al.
Pageof 20

Showing results (171-180 of 194) with videos related to

Sort By:
Pageof 20
Archives of Neurology|March 20, 2001
Frequency of tau gene mutations in familial and sporadic cases of non-Alzheimer dementiaP Poorkaj, M Grossman, E Steinbart, et al.
Human Genetics|November 1, 1991
Chromosome 1 Charcot-Marie-Tooth disease (CMT1B) locus in the Fc gamma receptor gene regionR V Lebo, P F Chance, P J Dyck, et al.
American Journal of Human Genetics|April 1, 1996
Gender difference in apolipoprotein E-associated risk for familial Alzheimer disease: a possible clue to the higher incidence of Alzheimer disease in womenH Payami, S Zareparsi, K R Montee, et al.
Neurology|December 17, 1998
Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia familiesM L Moseley, K A Benzow, L J Schut, et al.
Neurology|May 23, 2008
Late-onset hereditary axonal neuropathiesC L Bennett, V H Lawson, K L Brickell, et al.
Brain : a Journal of Neurology|September 1, 1999
The impact of different presenilin 1 andpresenilin 2 mutations on amyloid deposition, neurofibrillary changes and neuronal loss in the familial Alzheimer's disease brain: evidence for other phenotype-modifying factorsT Gómez-Isla, W B Growdon, M J McNamara, et al.
Annals of Neurology|June 1, 1997
Presenilin-1 protein expression in familial and sporadic Alzheimer's diseaseA I Levey, C J Heilman, J J Lah, et al.
Genes, Brain, and Behavior|October 19, 2017
Variants regulating ZBTB4 are associated with age-at-onset of Alzheimer's diseaseE E Blue, C-E Yu, T A Thornton, et al.
Neurology|May 5, 1998
Gender-related penetrance and de novo GTP-cyclohydrolase I gene mutations in dopa-responsive dystoniaY Furukawa, A E Lang, J M Trugman, et al.
Annals of Neurology|August 1, 1996
Amyloid beta protein (Abeta) deposition in chromosome 14-linked Alzheimer's disease: predominance of Abeta42(43)D M Mann, T Iwatsubo, N J Cairns, et al.
Pageof 20