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J P Bouchard

Showing results (61-70 of 96) with videos related to

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Neuromuscular Disorders : NMD|December 10, 1997
A pilot study on upper esophageal sphincter dilatation for the treatment of dysphagia in patients with oculopharyngeal muscular dystrophyJ Mathieu, G Lapointe, A Brassard, et al.
Advances in Neurology|January 1, 1993
Clinical and molecular genetic studies on autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS)A Richter, K Morgan, J P Bouchard, et al.
Archives of Physical Medicine and Rehabilitation|June 1, 1993
Task-specific physical therapy for optimization of gait recovery in acute stroke patientsC L Richards, F Malouin, S Wood-Dauphinee, et al.
Transplantation Proceedings|February 1, 1991
Expression of major histocompatibility complex antigens on human myoblastsR Roy, G Dansereau, J P Tremblay, et al.
Neuromuscular Disorders : NMD|November 26, 1998
Autosomal recessive spastic ataxia of Charlevoix-SaguenayJ P Bouchard, A Richter, J Mathieu, et al.
European Journal of Histochemistry : EJH|January 1, 1993
Rapid selection of donor myoblast clones for muscular dystrophy therapy using cell surface expression of NCAMM Belles-Isles, R Roy, G Dansereau, et al.
Cell Transplantation|March 1, 1993
Results of a triple blind clinical study of myoblast transplantations without immunosuppressive treatment in young boys with Duchenne muscular dystrophyJ P Tremblay, F Malouin, R Roy, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|August 23, 2011
Founder mutation for α-sarcoglycan-LGMD2D in a Magdalen Islands Acadian clusterM Tétreault, M Srour, J Allyson, 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.
Pageof 10

Showing results (61-70 of 96) with videos related to

Sort By:
Pageof 10
Neuromuscular Disorders : NMD|December 10, 1997
A pilot study on upper esophageal sphincter dilatation for the treatment of dysphagia in patients with oculopharyngeal muscular dystrophyJ Mathieu, G Lapointe, A Brassard, et al.
Advances in Neurology|January 1, 1993
Clinical and molecular genetic studies on autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS)A Richter, K Morgan, J P Bouchard, et al.
Archives of Physical Medicine and Rehabilitation|June 1, 1993
Task-specific physical therapy for optimization of gait recovery in acute stroke patientsC L Richards, F Malouin, S Wood-Dauphinee, et al.
Transplantation Proceedings|February 1, 1991
Expression of major histocompatibility complex antigens on human myoblastsR Roy, G Dansereau, J P Tremblay, et al.
Neuromuscular Disorders : NMD|November 26, 1998
Autosomal recessive spastic ataxia of Charlevoix-SaguenayJ P Bouchard, A Richter, J Mathieu, et al.
European Journal of Histochemistry : EJH|January 1, 1993
Rapid selection of donor myoblast clones for muscular dystrophy therapy using cell surface expression of NCAMM Belles-Isles, R Roy, G Dansereau, et al.
Cell Transplantation|March 1, 1993
Results of a triple blind clinical study of myoblast transplantations without immunosuppressive treatment in young boys with Duchenne muscular dystrophyJ P Tremblay, F Malouin, R Roy, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|August 23, 2011
Founder mutation for α-sarcoglycan-LGMD2D in a Magdalen Islands Acadian clusterM Tétreault, M Srour, J Allyson, 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.
Pageof 10