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J M Pinard

Showing results (21-30 of 34) with videos related to

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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 deficiencyS 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 syndromeL 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 mutationV 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 patientsA Palmini, F Andermann, J Aicardi, et al.
Neuropediatrics|September 10, 1999
Subcortical laminar heterotopia in two sisters and their mother: MRI, clinical findings and pathogenesisP H van der Valk, I Snoeck, L C Meiners, et al.
Cell|March 7, 1998
A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndromeV des Portes, J M Pinard, P Billuart, et al.
Human Molecular Genetics|June 9, 1998
doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH)V des Portes, F Francis, J M Pinard, et al.
Pageof 4

Showing results (21-30 of 34) with videos related to

Sort By:
Pageof 4
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 deficiencyS 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 syndromeL 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 mutationV 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 patientsA Palmini, F Andermann, J Aicardi, et al.
Neuropediatrics|September 10, 1999
Subcortical laminar heterotopia in two sisters and their mother: MRI, clinical findings and pathogenesisP H van der Valk, I Snoeck, L C Meiners, et al.
Cell|March 7, 1998
A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndromeV des Portes, J M Pinard, P Billuart, et al.
Human Molecular Genetics|June 9, 1998
doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH)V des Portes, F Francis, J M Pinard, et al.
Pageof 4