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Showing results (111-120 of 121) with videos related to

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 11, 2002
[Treatment of dystonia syndrome by chronic electric stimulation of the internal globus pallidus]P Coubes, L Cif, M Azais, et al.
American Journal of Human Genetics|February 17, 2001
Linkage of benign familial infantile convulsions to chromosome 16p12-q12 suggests allelism to the infantile convulsions and choreoathetosis syndromeR Caraballo, S Pavek, A Lemainque, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|March 13, 2014
Partial acute transverse myelitis is a predictor of multiple sclerosis in childrenP Meyer, N Leboucq, N Molinari, 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.
Brain : a Journal of Neurology|May 29, 2000
Levodopa-responsive dystonia. GTP cyclohydrolase I or parkin mutations?J Tassin, A Dürr, A M Bonnet, et al.
American Journal of Human Genetics|November 16, 2004
Mutations within the programmed cell death 10 gene cause cerebral cavernous malformationsF Bergametti, C Denier, P Labauge, et al.
Neurology|March 17, 2000
Homogeneous phenotype of the gypsy limb-girdle MD with the gamma-sarcoglycan C283Y mutationL Merlini, J C Kaplan, C Navarro, et al.
Journal of Medical Genetics|October 18, 2005
Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromesS Tezenas du Montcel, F Clot, M Vidailhet, et al.
Journal of Inherited Metabolic Disease|December 6, 2013
Update on transcobalamin deficiency: clinical presentation, treatment and outcomeY J Trakadis, A Alfares, O A Bodamer, et al.
Revue Neurologique|August 20, 2013
[Phenotypic heterogeneity and phenotype-genotype correlations in dystrophinopathies: Contribution of genetic and clinical databases]V Humbertclaude, D Hamroun, M-C Picot, et al.
Pageof 13

Showing results (111-120 of 121) with videos related to

Sort By:
Pageof 13
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 11, 2002
[Treatment of dystonia syndrome by chronic electric stimulation of the internal globus pallidus]P Coubes, L Cif, M Azais, et al.
American Journal of Human Genetics|February 17, 2001
Linkage of benign familial infantile convulsions to chromosome 16p12-q12 suggests allelism to the infantile convulsions and choreoathetosis syndromeR Caraballo, S Pavek, A Lemainque, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|March 13, 2014
Partial acute transverse myelitis is a predictor of multiple sclerosis in childrenP Meyer, N Leboucq, N Molinari, 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.
Brain : a Journal of Neurology|May 29, 2000
Levodopa-responsive dystonia. GTP cyclohydrolase I or parkin mutations?J Tassin, A Dürr, A M Bonnet, et al.
American Journal of Human Genetics|November 16, 2004
Mutations within the programmed cell death 10 gene cause cerebral cavernous malformationsF Bergametti, C Denier, P Labauge, et al.
Neurology|March 17, 2000
Homogeneous phenotype of the gypsy limb-girdle MD with the gamma-sarcoglycan C283Y mutationL Merlini, J C Kaplan, C Navarro, et al.
Journal of Medical Genetics|October 18, 2005
Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromesS Tezenas du Montcel, F Clot, M Vidailhet, et al.
Journal of Inherited Metabolic Disease|December 6, 2013
Update on transcobalamin deficiency: clinical presentation, treatment and outcomeY J Trakadis, A Alfares, O A Bodamer, et al.
Revue Neurologique|August 20, 2013
[Phenotypic heterogeneity and phenotype-genotype correlations in dystrophinopathies: Contribution of genetic and clinical databases]V Humbertclaude, D Hamroun, M-C Picot, et al.
Pageof 13