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P Verpillat

Showing results (31-40 of 36) 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.
Best Practice & Research. Clinical Obstetrics & Gynaecology|January 27, 2023
Comparative effectiveness of gonadotropins used for ovarian stimulation during assisted reproductive technologies (ART) in France: A real-world observational study from the French nationwide claims database (SNDS)M Grynberg, I Cedrin-Durnerin, F Raguideau, 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.
Journal of Medical Genetics|February 6, 2004
Melanocortin 1 receptor (MC1R) gene variants may increase the risk of melanoma in France independently of clinical risk factors and UV exposureE Matichard, P Verpillat, R Meziani, et al.
Neurology|August 1, 2007
Brain spect perfusion of frontotemporal dementia associated with motor neuron diseaseE Guedj, I Le Ber, L Lacomblez, 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.
Pageof 4

Showing results (31-40 of 36) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 36 results.
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.
Best Practice & Research. Clinical Obstetrics & Gynaecology|January 27, 2023
Comparative effectiveness of gonadotropins used for ovarian stimulation during assisted reproductive technologies (ART) in France: A real-world observational study from the French nationwide claims database (SNDS)M Grynberg, I Cedrin-Durnerin, F Raguideau, 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.
Journal of Medical Genetics|February 6, 2004
Melanocortin 1 receptor (MC1R) gene variants may increase the risk of melanoma in France independently of clinical risk factors and UV exposureE Matichard, P Verpillat, R Meziani, et al.
Neurology|August 1, 2007
Brain spect perfusion of frontotemporal dementia associated with motor neuron diseaseE Guedj, I Le Ber, L Lacomblez, 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.
Pageof 4