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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.
Proceedings of the National Academy of Sciences of the United States of America
|
September 2, 1998
The negative feedback actions of progesterone on gonadotropin-releasing hormone secretion are transduced by the classical progesterone receptor
D C Skinner, N P Evans, B Delaleu, 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.
Bone
|
July 27, 2013
A pre-clinical murine model of oral implant osseointegration
S Mouraret, D J Hunter, C Bardet, 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 Endocrinology
|
March 1, 1993
Inhibin and follicle-stimulating hormone levels in gonadotroph adenomas: evidence of a positive correlation with tumour volume in men
N Lahlou, E Le Nestour, P Chanson, 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.
Neuromuscular Disorders : NMD
|
December 10, 1997
A pilot study on upper esophageal sphincter dilatation for the treatment of dysphagia in patients with oculopharyngeal muscular dystrophy
J 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.
Page
of 38
Search research articles
Search
Showing results (241-250 of 372) with videos related to
Sort By:
Page
of 38
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.
Proceedings of the National Academy of Sciences of the United States of America
|
September 2, 1998
The negative feedback actions of progesterone on gonadotropin-releasing hormone secretion are transduced by the classical progesterone receptor
D C Skinner, N P Evans, B Delaleu, 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.
Bone
|
July 27, 2013
A pre-clinical murine model of oral implant osseointegration
S Mouraret, D J Hunter, C Bardet, 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 Endocrinology
|
March 1, 1993
Inhibin and follicle-stimulating hormone levels in gonadotroph adenomas: evidence of a positive correlation with tumour volume in men
N Lahlou, E Le Nestour, P Chanson, 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.
Neuromuscular Disorders : NMD
|
December 10, 1997
A pilot study on upper esophageal sphincter dilatation for the treatment of dysphagia in patients with oculopharyngeal muscular dystrophy
J 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.
Page
of 38