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N Dupré

Showing results (1-10 of 20) with videos related to

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Tissue Antigens|November 1, 1983
Exclusion of a tight linkage between familial polyposis coli and HLAC Raffoux, F Demenais, N Dupré, et al.
Annales De Medecine Interne|January 1, 1979
[Grawitz's tumor and provoked hyperlipemia (author's transl)]J Warter, D Storck, H Schirardin, et al.
Revue Neurologique|March 18, 2008
[Hereditary ataxias, spastic parapareses and neuropathies in Eastern Canada]N Dupré, N Chrestian, I Thiffault, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|March 17, 2001
A founder mutation in French-Canadian families with X-linked hereditary neuropathyN Dupré, L Cossette, C K Hand, et al.
Neurology|December 28, 2006
A founder haplotype for autosomal dominant sensory ataxia in Eastern CanadaP N Valdmanis, D Brunet, J St-Onge, et al.
Solid State Nuclear Magnetic Resonance|October 8, 2011
Quantitative MAS NMR characterization of the LiMn(1/2)Ni(1/2)O(2) electrode/electrolyte interphaseM Cuisinier, J F Martin, P Moreau, et al.
Physical Chemistry Chemical Physics : PCCP|October 1, 2014
Destructuring ionic liquids in ionogels: enhanced fragility for solid devicesA Guyomard-Lack, P-E Delannoy, N Dupré, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|August 19, 1999
Clinical and electrophysiological study in French-Canadian population with Charcot-Marie-tooth disease type 1A associated with 17p11.2 duplicationN Dupré, J P Bouchard, L Cossette, et al.
Annals of the New York Academy of Sciences|December 10, 1999
Phenotypic manifestations in French-Canadian populations with Charcot-Marie-Tooth disease type 1A associated with 17p11.2 duplicationN Dupré, J P Bouchard, L Cossette, et al.
Journal of Medical Genetics|August 3, 2004
A novel neurodegenerative disease characterised by posterior column ataxia and pyramidal tract involvement maps to chromosome 8p12-8q12.1P N Valdmanis, A A Simões Lopes, F Gros-Louis, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Tissue Antigens|November 1, 1983
Exclusion of a tight linkage between familial polyposis coli and HLAC Raffoux, F Demenais, N Dupré, et al.
Annales De Medecine Interne|January 1, 1979
[Grawitz's tumor and provoked hyperlipemia (author's transl)]J Warter, D Storck, H Schirardin, et al.
Revue Neurologique|March 18, 2008
[Hereditary ataxias, spastic parapareses and neuropathies in Eastern Canada]N Dupré, N Chrestian, I Thiffault, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|March 17, 2001
A founder mutation in French-Canadian families with X-linked hereditary neuropathyN Dupré, L Cossette, C K Hand, et al.
Neurology|December 28, 2006
A founder haplotype for autosomal dominant sensory ataxia in Eastern CanadaP N Valdmanis, D Brunet, J St-Onge, et al.
Solid State Nuclear Magnetic Resonance|October 8, 2011
Quantitative MAS NMR characterization of the LiMn(1/2)Ni(1/2)O(2) electrode/electrolyte interphaseM Cuisinier, J F Martin, P Moreau, et al.
Physical Chemistry Chemical Physics : PCCP|October 1, 2014
Destructuring ionic liquids in ionogels: enhanced fragility for solid devicesA Guyomard-Lack, P-E Delannoy, N Dupré, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|August 19, 1999
Clinical and electrophysiological study in French-Canadian population with Charcot-Marie-tooth disease type 1A associated with 17p11.2 duplicationN Dupré, J P Bouchard, L Cossette, et al.
Annals of the New York Academy of Sciences|December 10, 1999
Phenotypic manifestations in French-Canadian populations with Charcot-Marie-Tooth disease type 1A associated with 17p11.2 duplicationN Dupré, J P Bouchard, L Cossette, et al.
Journal of Medical Genetics|August 3, 2004
A novel neurodegenerative disease characterised by posterior column ataxia and pyramidal tract involvement maps to chromosome 8p12-8q12.1P N Valdmanis, A A Simões Lopes, F Gros-Louis, et al.
Pageof 2