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D Campion

Showing results (121-130 of 146) with videos related to

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Human Molecular Genetics|September 16, 1998
Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonismC Dumanchin, A Camuzat, D Campion, et al.
American Journal of Medical Genetics|July 23, 1998
Anticipation in schizophrenia: no evidence of expanded CAG/CTG repeat sequences in French families and sporadic casesC Laurent, C Zander, F Thibaut, et al.
Psychiatry Research|June 1, 1996
Association study between schizophrenia and monoamine oxidase A and B DNA polymorphismsB Coron, D Campion, F Thibaut, et al.
Journal of Medical Genetics|August 1, 1996
No founder effect in three novel Alzheimer's disease families with APP 717 Val-->Ile mutation. Clerget-darpoux. French Alzheimer's Disease Study GroupD Campion, A Brice, D Hannequin, et al.
European Journal of Human Genetics : EJHG|September 12, 2000
APOE promoter polymorphisms do not confer independent risk for Alzheimer's disease in a French populationL Zurutuza, P Verpillat, G Raux, et al.
Neurobiology of Disease|January 1, 1997
Manic depressive illness and tyrosine hydroxylase gene: linkage heterogeneity and associationA Malafosse, M Leboyer, T d'Amato, et al.
Neurology|February 28, 2007
Variations in the APP gene promoter region and risk of Alzheimer diseaseL Guyant-Maréchal, A Rovelet-Lecrux, L Goumidi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1997
No effect of the alpha1-antichymotrypsin A allele in Alzheimer's diseaseO Didierjean, M Martinez, D Campion, et al.
Neuroreport|July 8, 1996
A novel presenilin 1 mutation resulting in familial Alzheimer's disease with an onset age of 29 yearsD Campion, A Brice, C Dumanchin, et al.
Behavior Genetics|January 12, 2013
Xq27 FRAXA locus is a strong candidate for dyslexia: evidence from a genome-wide scan in French familiesM Huc-Chabrolle, C Charon, A Guilmatre, et al.
Pageof 15

Showing results (121-130 of 146) with videos related to

Sort By:
Pageof 15
Human Molecular Genetics|September 16, 1998
Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonismC Dumanchin, A Camuzat, D Campion, et al.
American Journal of Medical Genetics|July 23, 1998
Anticipation in schizophrenia: no evidence of expanded CAG/CTG repeat sequences in French families and sporadic casesC Laurent, C Zander, F Thibaut, et al.
Psychiatry Research|June 1, 1996
Association study between schizophrenia and monoamine oxidase A and B DNA polymorphismsB Coron, D Campion, F Thibaut, et al.
Journal of Medical Genetics|August 1, 1996
No founder effect in three novel Alzheimer's disease families with APP 717 Val-->Ile mutation. Clerget-darpoux. French Alzheimer's Disease Study GroupD Campion, A Brice, D Hannequin, et al.
European Journal of Human Genetics : EJHG|September 12, 2000
APOE promoter polymorphisms do not confer independent risk for Alzheimer's disease in a French populationL Zurutuza, P Verpillat, G Raux, et al.
Neurobiology of Disease|January 1, 1997
Manic depressive illness and tyrosine hydroxylase gene: linkage heterogeneity and associationA Malafosse, M Leboyer, T d'Amato, et al.
Neurology|February 28, 2007
Variations in the APP gene promoter region and risk of Alzheimer diseaseL Guyant-Maréchal, A Rovelet-Lecrux, L Goumidi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1997
No effect of the alpha1-antichymotrypsin A allele in Alzheimer's diseaseO Didierjean, M Martinez, D Campion, et al.
Neuroreport|July 8, 1996
A novel presenilin 1 mutation resulting in familial Alzheimer's disease with an onset age of 29 yearsD Campion, A Brice, C Dumanchin, et al.
Behavior Genetics|January 12, 2013
Xq27 FRAXA locus is a strong candidate for dyslexia: evidence from a genome-wide scan in French familiesM Huc-Chabrolle, C Charon, A Guilmatre, et al.
Pageof 15