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B Moulard

Showing results (1-10 of 13) with videos related to

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Revue Neurologique|April 27, 2002
[Genetic aspects of epilepsy: current knowledge and perspectives]A Malafosse, B Moulard
Human Mutation|August 3, 2000
Study of the voltage-gated sodium channel beta 1 subunit gene (SCN1B) in the benign familial infantile convulsions syndrome (BFIC)B Moulard, C Buresi, A Malafosse
Revue Neurologique|October 18, 2000
[Recent insights about genetics of human idiopathic epilepsies and febrile seizures]B Moulard, A Crespel, A Malafosse, et al.
Journal of the Neurological Sciences|August 1, 1996
Apolipoprotein E genotyping in sporadic amyotrophic lateral sclerosis: evidence for a major influence on the clinical presentation and prognosisB Moulard, A Sefiani, A Laamri, et al.
Revue Neurologique|June 1, 1997
[Clinical study of familial forms of amyotrophic lateral sclerosis. Review of the literature]B Moulard, W Camu, A Malafosse, et al.
American Journal of Human Genetics|October 16, 1999
Identification of a new locus for generalized epilepsy with febrile seizures plus (GEFS+) on chromosome 2q24-q33B Moulard, M Guipponi, D Chaigne, et al.
Annals of Neurology|May 19, 1998
Association between centromeric deletions of the SMN gene and sporadic adult-onset lower motor neuron diseaseB Moulard, F Salachas, B Chassande, et al.
Journal of the Neurological Sciences|August 17, 1999
Genetics of familial ALS and consequences for diagnosis. French ALS Research GroupW Camu, J Khoris, B Moulard, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|August 26, 1998
Identification of six novel SOD1 gene mutations in familial amyotrophic lateral sclerosisY Boukaftane, J Khoris, B Moulard, et al.
Neurobiology of Disease|November 1, 1994
A nonsense mutation in the alpha4 subunit of the nicotinic acetylcholine receptor (CHRNA4) cosegregates with 20q-linked benign neonatal familial convulsions (EBNI)C Beck, B Moulard, O Steinlein, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Revue Neurologique|April 27, 2002
[Genetic aspects of epilepsy: current knowledge and perspectives]A Malafosse, B Moulard
Human Mutation|August 3, 2000
Study of the voltage-gated sodium channel beta 1 subunit gene (SCN1B) in the benign familial infantile convulsions syndrome (BFIC)B Moulard, C Buresi, A Malafosse
Revue Neurologique|October 18, 2000
[Recent insights about genetics of human idiopathic epilepsies and febrile seizures]B Moulard, A Crespel, A Malafosse, et al.
Journal of the Neurological Sciences|August 1, 1996
Apolipoprotein E genotyping in sporadic amyotrophic lateral sclerosis: evidence for a major influence on the clinical presentation and prognosisB Moulard, A Sefiani, A Laamri, et al.
Revue Neurologique|June 1, 1997
[Clinical study of familial forms of amyotrophic lateral sclerosis. Review of the literature]B Moulard, W Camu, A Malafosse, et al.
American Journal of Human Genetics|October 16, 1999
Identification of a new locus for generalized epilepsy with febrile seizures plus (GEFS+) on chromosome 2q24-q33B Moulard, M Guipponi, D Chaigne, et al.
Annals of Neurology|May 19, 1998
Association between centromeric deletions of the SMN gene and sporadic adult-onset lower motor neuron diseaseB Moulard, F Salachas, B Chassande, et al.
Journal of the Neurological Sciences|August 17, 1999
Genetics of familial ALS and consequences for diagnosis. French ALS Research GroupW Camu, J Khoris, B Moulard, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|August 26, 1998
Identification of six novel SOD1 gene mutations in familial amyotrophic lateral sclerosisY Boukaftane, J Khoris, B Moulard, et al.
Neurobiology of Disease|November 1, 1994
A nonsense mutation in the alpha4 subunit of the nicotinic acetylcholine receptor (CHRNA4) cosegregates with 20q-linked benign neonatal familial convulsions (EBNI)C Beck, B Moulard, O Steinlein, et al.
Pageof 2