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P Bouchard

Showing results (351-360 of 372) with videos related to

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Neurology|November 23, 2000
Oculopharyngeal MD among Bukhara Jews is due to a founder (GCG)9 mutation in the PABP2 geneS C Blumen, A D Korczyn, H Lavoie, et al.
European Journal of Endocrinology|March 18, 2009
Merits and pitfalls of mifepristone in Cushing's syndromeF Castinetti, M Fassnacht, S Johanssen, et al.
Nature Genetics|February 2, 2000
ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORFJ C Engert, P Bérubé, J Mercier, et al.
Neurology|August 13, 2008
Association of paraoxonase gene cluster polymorphisms with ALS in France, Quebec, and SwedenP N Valdmanis, E Kabashi, A Dyck, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|March 1, 2005
Randomized study of once-weekly interferon beta-1la therapy in relapsing multiple sclerosis: three-year data from the OWIMS studyM S Freedman, G S Francis, E A C M Sanders, et al.
Human Reproduction (Oxford, England)|June 19, 2018
Impact on testicular function of a single ablative activity of 3.7 GBq radioactive iodine for differentiated thyroid carcinomaN Bourcigaux, C Rubino, I Berthaud, et al.
The Journal of Experimental Medicine|August 4, 1998
Interleukin 12-mediated prevention of spontaneous mammary adenocarcinomas in two lines of Her-2/neu transgenic miceK Boggio, G Nicoletti, E Di Carlo, et al.
Neurology|September 11, 2009
Mutations in FUS cause FALS and SALS in French and French Canadian populationsV V Belzil, P N Valdmanis, P A Dion, et al.
European Journal of Endocrinology|May 10, 2011
Gender-related differences in MEN1 lesion occurrence and diagnosis: a cohort study of 734 cases from the Groupe d'etude des Tumeurs EndocrinesP Goudet, C Bonithon-Kopp, A Murat, et al.
Nature Genetics|February 14, 1998
Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophyB Brais, J P Bouchard, Y G Xie, et al.
Pageof 38

Showing results (351-360 of 372) with videos related to

Sort By:
Pageof 38
Neurology|November 23, 2000
Oculopharyngeal MD among Bukhara Jews is due to a founder (GCG)9 mutation in the PABP2 geneS C Blumen, A D Korczyn, H Lavoie, et al.
European Journal of Endocrinology|March 18, 2009
Merits and pitfalls of mifepristone in Cushing's syndromeF Castinetti, M Fassnacht, S Johanssen, et al.
Nature Genetics|February 2, 2000
ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORFJ C Engert, P Bérubé, J Mercier, et al.
Neurology|August 13, 2008
Association of paraoxonase gene cluster polymorphisms with ALS in France, Quebec, and SwedenP N Valdmanis, E Kabashi, A Dyck, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|March 1, 2005
Randomized study of once-weekly interferon beta-1la therapy in relapsing multiple sclerosis: three-year data from the OWIMS studyM S Freedman, G S Francis, E A C M Sanders, et al.
Human Reproduction (Oxford, England)|June 19, 2018
Impact on testicular function of a single ablative activity of 3.7 GBq radioactive iodine for differentiated thyroid carcinomaN Bourcigaux, C Rubino, I Berthaud, et al.
The Journal of Experimental Medicine|August 4, 1998
Interleukin 12-mediated prevention of spontaneous mammary adenocarcinomas in two lines of Her-2/neu transgenic miceK Boggio, G Nicoletti, E Di Carlo, et al.
Neurology|September 11, 2009
Mutations in FUS cause FALS and SALS in French and French Canadian populationsV V Belzil, P N Valdmanis, P A Dion, et al.
European Journal of Endocrinology|May 10, 2011
Gender-related differences in MEN1 lesion occurrence and diagnosis: a cohort study of 734 cases from the Groupe d'etude des Tumeurs EndocrinesP Goudet, C Bonithon-Kopp, A Murat, et al.
Nature Genetics|February 14, 1998
Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophyB Brais, J P Bouchard, Y G Xie, et al.
Pageof 38