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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 mutants
P 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 ataxia
J 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-Saguenay
J Mercier, C Prévost, J C Engert, et al.
Transplantation Proceedings
|
February 1, 1993
Antibody formation after myoblast transplantation in Duchenne-dystrophic patients, donor HLA compatible
R Roy, J P Tremblay, J Huard, et al.
Transplantation Proceedings
|
December 1, 1992
Human myoblast transplantation between immunohistocompatible donors and recipients produces immune reactions
J 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 neuropathy
N 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 schizophrenia
A 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 ataxia
G 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 sequence
J 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 dystrophy
J Huard, J P Bouchard, R Roy, et al.
Page
of 10
Search research articles
Search
Showing results (51-60 of 96) with videos related to
Sort By:
Page
of 10
Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire
|
January 12, 2007
K-Cl cotransport in red blood cells from patients with KCC3 isoform mutants
P 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 ataxia
J 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-Saguenay
J Mercier, C Prévost, J C Engert, et al.
Transplantation Proceedings
|
February 1, 1993
Antibody formation after myoblast transplantation in Duchenne-dystrophic patients, donor HLA compatible
R Roy, J P Tremblay, J Huard, et al.
Transplantation Proceedings
|
December 1, 1992
Human myoblast transplantation between immunohistocompatible donors and recipients produces immune reactions
J 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 neuropathy
N 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 schizophrenia
A 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 ataxia
G 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 sequence
J 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 dystrophy
J Huard, J P Bouchard, R Roy, et al.
Page
of 10