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Human Genetics
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July 8, 1999
Association between coding variability in the LRP gene and the risk of late-onset Alzheimer's disease
F Wavrant-DeVrièze, J C Lambert, L Stas, et al.
Journal of Human Hypertension
|
August 30, 2000
Association of hypertensive status and its drug treatment with lipid and haemostatic factors in middle-aged men: the PRIME study
P Marques-Vidal, M Montaye, B Haas, et al.
Neurology
|
August 19, 2011
Systemic chemokine levels, coronary heart disease, and ischemic stroke events: the PRIME study
F Canouï-Poitrine, G Luc, Z Mallat, et al.
Human Molecular Genetics
|
August 13, 1998
Pronounced impact of Th1/E47cs mutation compared with -491 AT mutation on neural APOE gene expression and risk of developing Alzheimer's disease
J C Lambert, C Berr, F Pasquier, et al.
Journal of Human Hypertension
|
September 6, 2002
Efficacy of very low dose perindopril 2 mg/indapamide 0.625 mg combination on left ventricular hypertrophy in hypertensive patients: the P.I.C.X.E.L. study rationale and design
P Gosse, O Dubourg, P Guéret, et al.
Molecular Psychiatry
|
March 16, 2011
Alzheimer risk associated with a copy number variation in the complement receptor 1 increasing C3b/C4b binding sites
N Brouwers, C Van Cauwenberghe, S Engelborghs, et al.
Molecular Psychiatry
|
June 21, 2007
Evidence for the association of the S100beta gene with low cognitive performance and dementia in the elderly
J-C Lambert, S Ferreira, J Gussekloo, et al.
Human Molecular Genetics
|
September 26, 2000
The transcriptional factor LBP-1c/CP2/LSF gene on chromosome 12 is a genetic determinant of Alzheimer's disease
J C Lambert, L Goumidi, F W Vrièze, et al.
Scientific Reports
|
March 8, 2019
Minor allele of the factor V K858R variant protects from venous thrombosis only in non-carriers of factor V Leiden mutation
M Ibrahim-Kosta, P Suchon, F Couturaud, et al.
European Heart Journal
|
October 26, 1999
Identification of a genetic risk factor for idiopathic dilated cardiomyopathy. Involvement of a polymorphism in the endothelin receptor type A gene. CARDIGENE group
P Charron, F Tesson, O Poirier, et al.
Page
of 23
Search research articles
Search
Showing results (191-200 of 225) with videos related to
Sort By:
Page
of 23
Human Genetics
|
July 8, 1999
Association between coding variability in the LRP gene and the risk of late-onset Alzheimer's disease
F Wavrant-DeVrièze, J C Lambert, L Stas, et al.
Journal of Human Hypertension
|
August 30, 2000
Association of hypertensive status and its drug treatment with lipid and haemostatic factors in middle-aged men: the PRIME study
P Marques-Vidal, M Montaye, B Haas, et al.
Neurology
|
August 19, 2011
Systemic chemokine levels, coronary heart disease, and ischemic stroke events: the PRIME study
F Canouï-Poitrine, G Luc, Z Mallat, et al.
Human Molecular Genetics
|
August 13, 1998
Pronounced impact of Th1/E47cs mutation compared with -491 AT mutation on neural APOE gene expression and risk of developing Alzheimer's disease
J C Lambert, C Berr, F Pasquier, et al.
Journal of Human Hypertension
|
September 6, 2002
Efficacy of very low dose perindopril 2 mg/indapamide 0.625 mg combination on left ventricular hypertrophy in hypertensive patients: the P.I.C.X.E.L. study rationale and design
P Gosse, O Dubourg, P Guéret, et al.
Molecular Psychiatry
|
March 16, 2011
Alzheimer risk associated with a copy number variation in the complement receptor 1 increasing C3b/C4b binding sites
N Brouwers, C Van Cauwenberghe, S Engelborghs, et al.
Molecular Psychiatry
|
June 21, 2007
Evidence for the association of the S100beta gene with low cognitive performance and dementia in the elderly
J-C Lambert, S Ferreira, J Gussekloo, et al.
Human Molecular Genetics
|
September 26, 2000
The transcriptional factor LBP-1c/CP2/LSF gene on chromosome 12 is a genetic determinant of Alzheimer's disease
J C Lambert, L Goumidi, F W Vrièze, et al.
Scientific Reports
|
March 8, 2019
Minor allele of the factor V K858R variant protects from venous thrombosis only in non-carriers of factor V Leiden mutation
M Ibrahim-Kosta, P Suchon, F Couturaud, et al.
European Heart Journal
|
October 26, 1999
Identification of a genetic risk factor for idiopathic dilated cardiomyopathy. Involvement of a polymorphism in the endothelin receptor type A gene. CARDIGENE group
P Charron, F Tesson, O Poirier, et al.
Page
of 23