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J P Bouchard

Showing results (51-60 of 96) with videos related to

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Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire|January 12, 2007
K-Cl cotransport in red blood cells from patients with KCC3 isoform mutantsP K Lauf, N C Adragna, N Dupre, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|November 1, 1976
Nerve conduction studies and electromyography in Friedreich's ataxiaJ M Peyronnard, L Lapointe, J P Bouchard, et al.
Genetic Testing|January 15, 2002
Rapid detection of the sacsin mutations causing autosomal recessive spastic ataxia of Charlevoix-SaguenayJ Mercier, C Prévost, J C Engert, et al.
Transplantation Proceedings|February 1, 1993
Antibody formation after myoblast transplantation in Duchenne-dystrophic patients, donor HLA compatibleR Roy, J P Tremblay, J Huard, et al.
Transplantation Proceedings|December 1, 1992
Human myoblast transplantation between immunohistocompatible donors and recipients produces immune reactionsJ Huard, R Roy, J P Bouchard, 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.
Lancet (London, England)|November 18, 1978
Rapid inactivation of enkephalin-like material by C.S.F. in chronic schizophreniaA Dupont, A Villeneuve, J P Bouchard, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|November 1, 1976
Clinical description and roentgenologic evaluation of patients with Friedreich's ataxiaG Geoffroy, A Barbeau, G Breton, et al.
Brain and Cognition|July 1, 1997
Role of the striatum, cerebellum, and frontal lobes in the learning of a visuomotor sequenceJ Doyon, D Gaudreau, R Laforce, et al.
Clinical Science (London, England : 1979)|August 1, 1991
Myoblast transplantation produced dystrophin-positive muscle fibres in a 16-year-old patient with Duchenne muscular dystrophyJ Huard, J P Bouchard, R Roy, et al.
Pageof 10

Showing results (51-60 of 96) with videos related to

Sort By:
Pageof 10
Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire|January 12, 2007
K-Cl cotransport in red blood cells from patients with KCC3 isoform mutantsP K Lauf, N C Adragna, N Dupre, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|November 1, 1976
Nerve conduction studies and electromyography in Friedreich's ataxiaJ M Peyronnard, L Lapointe, J P Bouchard, et al.
Genetic Testing|January 15, 2002
Rapid detection of the sacsin mutations causing autosomal recessive spastic ataxia of Charlevoix-SaguenayJ Mercier, C Prévost, J C Engert, et al.
Transplantation Proceedings|February 1, 1993
Antibody formation after myoblast transplantation in Duchenne-dystrophic patients, donor HLA compatibleR Roy, J P Tremblay, J Huard, et al.
Transplantation Proceedings|December 1, 1992
Human myoblast transplantation between immunohistocompatible donors and recipients produces immune reactionsJ Huard, R Roy, J P Bouchard, 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.
Lancet (London, England)|November 18, 1978
Rapid inactivation of enkephalin-like material by C.S.F. in chronic schizophreniaA Dupont, A Villeneuve, J P Bouchard, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|November 1, 1976
Clinical description and roentgenologic evaluation of patients with Friedreich's ataxiaG Geoffroy, A Barbeau, G Breton, et al.
Brain and Cognition|July 1, 1997
Role of the striatum, cerebellum, and frontal lobes in the learning of a visuomotor sequenceJ Doyon, D Gaudreau, R Laforce, et al.
Clinical Science (London, England : 1979)|August 1, 1991
Myoblast transplantation produced dystrophin-positive muscle fibres in a 16-year-old patient with Duchenne muscular dystrophyJ Huard, J P Bouchard, R Roy, et al.
Pageof 10