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Neurology|February 26, 2004
Levetiracetam in progressive myoclonic epilepsy: an exploratory study in 9 patientsC Crest, S Dupont, E Leguern, et al.Dialogues in Clinical Neuroscience|October 29, 2011
Genetics of inherited human epilepsiesI Gourfinkel-An, S Baulac, A Brice, et al.Revue Neurologique|July 23, 2004
[Recent insights into the implication of ion channels in familial forms of epilepsies associated or non associated to febrile convulsions]I Gourfinkel-An, S Baulac, R Nabbout, et al.Human Genetics|June 16, 1999
The human neuregulin-2 (NRG2) gene: cloning, mapping and evaluation as a candidate for the autosomal recessive form of Charcot-Marie-Tooth disease linked to 5qH Z Ring, H Chang, A Guilbot, et al.Placenta|December 4, 2014
The involvement of the trans-generational effect in the high incidence of the hydatidiform mole in AfricaP Coullin, A L Diatta, H Boufettal, et al.Muscle & Nerve|September 26, 2000
Phenotypic and genetic study of a family with hereditary sensory neuropathy and prominent weaknessO Dubourg, C Barhoumi, H Azzedine, et al.Neurology|April 1, 1997
A clinical, electrophysiologic, neuropathologic, and genetic study of two large Algerian families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth diseaseM Kessali, R Zemmouri, A Guilbot, et al.Human Molecular Genetics|October 1, 1996
Homozygosity mapping of an autosomal recessive form of demyelinating Charcot-Marie-Tooth disease to chromosome 5q23-q33E LeGuern, A Guilbot, M Kessali, et al.Cytogenetics and Cell Genetics|January 1, 1996
Microsatellite mapping of the deletion in patients with hereditary neuropathy with liability to pressure palsies (HNPP): new molecular tools for the study of the region 17p12 --> p11 and for diagnosisE LeGuern, N Ravise, R Gouider, et al.Annals of Neurology|January 1, 1997
Patients homozygous for the 17p11.2 duplication in Charcot-Marie-Tooth type 1A diseaseE LeGuern, R Gouider, D Mabin, et al.Pageof 7