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Neurology
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October 29, 2003
Very early onset AD with a de novo mutation in the presenilin 1 gene (Met 233 Leu)
F Portet, Y Dauvilliers, D Campion, et al.
Schizophrenia Research
|
April 29, 1998
No association of apolipoprotein epsilon 4 allele with schizophrenia even in cognitively impaired patients
F Thibaut, B Coron, D Hannequin, et al.
Journal of Medical Genetics
|
January 15, 2003
The severe form of type I hyperprolinaemia results from homozygous inactivation of the PRODH gene
H Jacquet, J Berthelot, C Bonnemains, et al.
European Psychiatry : the Journal of the Association of European Psychiatrists
|
November 26, 1999
Apolipoprotein E-varepsilon4 frequency in deficit schizophrenia
F Thibaut, A Van Der Elst, D Campion, et al.
Neurology
|
November 30, 2000
Dementia with prominent frontotemporal features associated with L113P presenilin 1 mutation
G Raux, R Gantier, C Thomas-Anterion, et al.
Biological Psychiatry
|
October 6, 1997
Serotonin transporter gene polymorphism and schizophrenia: an association study
F Bonnet-Brilhault, C Laurent, F Thibaut, et al.
Psychiatry Research
|
May 23, 2001
No evidence for linkage between COMT and schizophrenia in a French population
M de Chaldée, M Corbex, D Campion, et al.
Journal of Medical Genetics
|
July 22, 2005
Molecular diagnosis of autosomal dominant early onset Alzheimer's disease: an update
G Raux, L Guyant-Maréchal, C Martin, et al.
Revue Neurologique
|
December 1, 1995
[Phenotype of familial forms of early-onset Alzheimer's disease linked to chromosome 14. Clinical and neuropsychological characteristics of a large group]
D Hannequin, D Campion, S Tardieu, et al.
The Journal of Applied Psychology
|
October 19, 2023
Using natural language processing to increase prediction and reduce subgroup differences in personnel selection decisions
Emily D Campion, Michael A Campion, James Johnson, et al.
Page
of 15
Search research articles
Search
Showing results (71-80 of 146) with videos related to
Sort By:
Page
of 15
Neurology
|
October 29, 2003
Very early onset AD with a de novo mutation in the presenilin 1 gene (Met 233 Leu)
F Portet, Y Dauvilliers, D Campion, et al.
Schizophrenia Research
|
April 29, 1998
No association of apolipoprotein epsilon 4 allele with schizophrenia even in cognitively impaired patients
F Thibaut, B Coron, D Hannequin, et al.
Journal of Medical Genetics
|
January 15, 2003
The severe form of type I hyperprolinaemia results from homozygous inactivation of the PRODH gene
H Jacquet, J Berthelot, C Bonnemains, et al.
European Psychiatry : the Journal of the Association of European Psychiatrists
|
November 26, 1999
Apolipoprotein E-varepsilon4 frequency in deficit schizophrenia
F Thibaut, A Van Der Elst, D Campion, et al.
Neurology
|
November 30, 2000
Dementia with prominent frontotemporal features associated with L113P presenilin 1 mutation
G Raux, R Gantier, C Thomas-Anterion, et al.
Biological Psychiatry
|
October 6, 1997
Serotonin transporter gene polymorphism and schizophrenia: an association study
F Bonnet-Brilhault, C Laurent, F Thibaut, et al.
Psychiatry Research
|
May 23, 2001
No evidence for linkage between COMT and schizophrenia in a French population
M de Chaldée, M Corbex, D Campion, et al.
Journal of Medical Genetics
|
July 22, 2005
Molecular diagnosis of autosomal dominant early onset Alzheimer's disease: an update
G Raux, L Guyant-Maréchal, C Martin, et al.
Revue Neurologique
|
December 1, 1995
[Phenotype of familial forms of early-onset Alzheimer's disease linked to chromosome 14. Clinical and neuropsychological characteristics of a large group]
D Hannequin, D Campion, S Tardieu, et al.
The Journal of Applied Psychology
|
October 19, 2023
Using natural language processing to increase prediction and reduce subgroup differences in personnel selection decisions
Emily D Campion, Michael A Campion, James Johnson, et al.
Page
of 15