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

D Campion

Showing results (131-140 of 146) with videos related to

Pageof 15
Sort By:
Revue Neurologique|December 1, 1996
[Genetics of dominant autosomal forms of Alzheimer disease: 3 genes and one phenotype. Groupe de Recherche Francais sur la Maladie d'Alzheimer]A Brice, B Dubois, Y Agid, et al.
American Journal of Human Genetics|August 12, 1999
Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrumD Campion, C Dumanchin, D Hannequin, et al.
Molecular Psychiatry|October 21, 2004
Hyperprolinemia is a risk factor for schizoaffective disorderH Jacquet, C Demily, E Houy, et al.
Molecular Psychiatry|July 22, 2015
De novo deleterious genetic variations target a biological network centered on Aβ peptide in early-onset Alzheimer diseaseA Rovelet-Lecrux, C Charbonnier, D Wallon, et al.
Molecular Psychiatry|April 5, 2012
High frequency of potentially pathogenic SORL1 mutations in autosomal dominant early-onset Alzheimer diseaseC Pottier, D Hannequin, S Coutant, et al.
L'Encephale|June 24, 2017
[Association between the violence in the community and the aggressive behaviors of psychotics during their hospitalizations]M Rothärmel, M-F Poirier, G Levacon, et al.
Human Molecular Genetics|July 1, 1996
Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrantR Sherrington, S Froelich, S Sorbi, et al.
American Journal of Human Genetics|February 1, 1997
Apolipoprotein E and Alzheimer disease: genotype-specific risks by age and sexH Bickeböller, D Campion, A Brice, et al.
Neurology|May 13, 2009
Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron diseaseI Le Ber, A Camuzat, E Berger, et al.
Molecular Psychiatry|August 26, 2015
SORL1 rare variants: a major risk factor for familial early-onset Alzheimer's diseaseG Nicolas, C Charbonnier, D Wallon, et al.
Pageof 15

Showing results (131-140 of 146) with videos related to

Sort By:
Pageof 15
Revue Neurologique|December 1, 1996
[Genetics of dominant autosomal forms of Alzheimer disease: 3 genes and one phenotype. Groupe de Recherche Francais sur la Maladie d'Alzheimer]A Brice, B Dubois, Y Agid, et al.
American Journal of Human Genetics|August 12, 1999
Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrumD Campion, C Dumanchin, D Hannequin, et al.
Molecular Psychiatry|October 21, 2004
Hyperprolinemia is a risk factor for schizoaffective disorderH Jacquet, C Demily, E Houy, et al.
Molecular Psychiatry|July 22, 2015
De novo deleterious genetic variations target a biological network centered on Aβ peptide in early-onset Alzheimer diseaseA Rovelet-Lecrux, C Charbonnier, D Wallon, et al.
Molecular Psychiatry|April 5, 2012
High frequency of potentially pathogenic SORL1 mutations in autosomal dominant early-onset Alzheimer diseaseC Pottier, D Hannequin, S Coutant, et al.
L'Encephale|June 24, 2017
[Association between the violence in the community and the aggressive behaviors of psychotics during their hospitalizations]M Rothärmel, M-F Poirier, G Levacon, et al.
Human Molecular Genetics|July 1, 1996
Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrantR Sherrington, S Froelich, S Sorbi, et al.
American Journal of Human Genetics|February 1, 1997
Apolipoprotein E and Alzheimer disease: genotype-specific risks by age and sexH Bickeböller, D Campion, A Brice, et al.
Neurology|May 13, 2009
Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron diseaseI Le Ber, A Camuzat, E Berger, et al.
Molecular Psychiatry|August 26, 2015
SORL1 rare variants: a major risk factor for familial early-onset Alzheimer's diseaseG Nicolas, C Charbonnier, D Wallon, et al.
Pageof 15