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OTJR : Occupation, Participation and Health
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January 4, 2021
Pilot Study of French-Canadian Lifestyle Redesign<sup>®</sup> for Chronic Pain Management
É Lagueux, J Masse, M Levasseur, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
July 11, 2002
[Clinical results and long-term neuropsychological status after hemispherectomy]
C Bulteau, O Delalande, V Buret, et al.
Revue Neurologique
|
May 20, 2006
[Neurological aspects of Fabry's disease]
P Clavelou, G Besson, C Elziere, et al.
Radiology
|
March 12, 1998
Congenital muscular dystrophy: use of brain MR imaging findings to predict merosin deficiency
S Lamer, R Y Carlier, J M Pinard, et al.
Journal of Medical Genetics
|
October 1, 1992
De novo t(X;21)(q28;q11) in a girl with phenotypic features of Williams-Beuren syndrome
L Telvi, J M Pinard, R Ion, et al.
Seizure
|
May 25, 2002
So-called 'cryptogenic' partial seizures resulting from a subtle cortical dysgenesis due to a doublecortin gene mutation
V des Portes, L Abaoub, A Joannard, et al.
Revue Neurologique
|
January 1, 1994
[GM2-Gangliosidosis variant B1 disclosed during adolescence by an isolated multi-systemic involvement of the central and peripheral nervous systems]
P Le Coz, E Assouline, M T Vanier, et al.
Neurology
|
October 1, 1991
Diffuse cortical dysplasia, or the 'double cortex' syndrome: the clinical and epileptic spectrum in 10 patients
A Palmini, F Andermann, J Aicardi, et al.
Physical Review Letters
|
October 10, 2006
High-sensitivity optical monitoring of a micromechanical resonator with a quantum-limited optomechanical sensor
O Arcizet, P-F Cohadon, T Briant, et al.
Neuropediatrics
|
September 10, 1999
Subcortical laminar heterotopia in two sisters and their mother: MRI, clinical findings and pathogenesis
P H van der Valk, I Snoeck, L C Meiners, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 67) with videos related to
Sort By:
Page
of 7
OTJR : Occupation, Participation and Health
|
January 4, 2021
Pilot Study of French-Canadian Lifestyle Redesign<sup>®</sup> for Chronic Pain Management
É Lagueux, J Masse, M Levasseur, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
July 11, 2002
[Clinical results and long-term neuropsychological status after hemispherectomy]
C Bulteau, O Delalande, V Buret, et al.
Revue Neurologique
|
May 20, 2006
[Neurological aspects of Fabry's disease]
P Clavelou, G Besson, C Elziere, et al.
Radiology
|
March 12, 1998
Congenital muscular dystrophy: use of brain MR imaging findings to predict merosin deficiency
S Lamer, R Y Carlier, J M Pinard, et al.
Journal of Medical Genetics
|
October 1, 1992
De novo t(X;21)(q28;q11) in a girl with phenotypic features of Williams-Beuren syndrome
L Telvi, J M Pinard, R Ion, et al.
Seizure
|
May 25, 2002
So-called 'cryptogenic' partial seizures resulting from a subtle cortical dysgenesis due to a doublecortin gene mutation
V des Portes, L Abaoub, A Joannard, et al.
Revue Neurologique
|
January 1, 1994
[GM2-Gangliosidosis variant B1 disclosed during adolescence by an isolated multi-systemic involvement of the central and peripheral nervous systems]
P Le Coz, E Assouline, M T Vanier, et al.
Neurology
|
October 1, 1991
Diffuse cortical dysplasia, or the 'double cortex' syndrome: the clinical and epileptic spectrum in 10 patients
A Palmini, F Andermann, J Aicardi, et al.
Physical Review Letters
|
October 10, 2006
High-sensitivity optical monitoring of a micromechanical resonator with a quantum-limited optomechanical sensor
O Arcizet, P-F Cohadon, T Briant, et al.
Neuropediatrics
|
September 10, 1999
Subcortical laminar heterotopia in two sisters and their mother: MRI, clinical findings and pathogenesis
P H van der Valk, I Snoeck, L C Meiners, et al.
Page
of 7