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E Andermann

Showing results (121-130 of 159) with videos related to

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Brain Pathology (Zurich, Switzerland)|October 1, 1993
Searching for human epilepsy genes: a progress reportM Leppert, W M McMahon, T G Quattlebaum, et al.
Annals of Neurology|October 1, 1988
Leukoencephalopathy among native Indian infants in northern Quebec and ManitobaD N Black, F Booth, G V Watters, et al.
Epilepsy Research|November 1, 1995
Genetic linkage studies in familial frontal epilepsy: exclusion of the human chromosome regions homologous to the El-1 mouse locusI Lopes-Cendes, H A Phillips, I E Scheffer, et al.
Neurology|October 27, 2004
Mutations and polymorphisms of the CLCN2 gene in idiopathic epilepsyD D'Agostino, M Bertelli, S Gallo, et al.
Brain : a Journal of Neurology|February 1, 1995
Autosomal dominant nocturnal frontal lobe epilepsy. A distinctive clinical disorderI E Scheffer, K P Bhatia, I Lopes-Cendes, et al.
Neurology|March 4, 1998
Pedigree analysis of French Canadian families with T14484C Leber's hereditary optic neuropathyC Macmillan, T Kirkham, K Fu, et al.
Neurology|March 23, 2007
Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3P Hedera, M A Blair, E Andermann, et al.
Lancet (London, England)|February 26, 1994
Autosomal dominant frontal epilepsy misdiagnosed as sleep disorderI E Scheffer, K P Bhatia, I Lopes-Cendes, et al.
American Journal of Human Genetics|January 1, 1996
The gene responsible for a severe form of peripheral neuropathy and agenesis of the corpus callosum maps to chromosome 15qL K Casaubon, M Melanson, I Lopes-Cendes, et al.
Neurology|November 18, 1998
Surgical treatment of epilepsy in tuberous sclerosis: strategies and results in 18 patientsM M Guerreiro, F Andermann, E Andermann, et al.
Pageof 16

Showing results (121-130 of 159) with videos related to

Sort By:
Pageof 16
Brain Pathology (Zurich, Switzerland)|October 1, 1993
Searching for human epilepsy genes: a progress reportM Leppert, W M McMahon, T G Quattlebaum, et al.
Annals of Neurology|October 1, 1988
Leukoencephalopathy among native Indian infants in northern Quebec and ManitobaD N Black, F Booth, G V Watters, et al.
Epilepsy Research|November 1, 1995
Genetic linkage studies in familial frontal epilepsy: exclusion of the human chromosome regions homologous to the El-1 mouse locusI Lopes-Cendes, H A Phillips, I E Scheffer, et al.
Neurology|October 27, 2004
Mutations and polymorphisms of the CLCN2 gene in idiopathic epilepsyD D'Agostino, M Bertelli, S Gallo, et al.
Brain : a Journal of Neurology|February 1, 1995
Autosomal dominant nocturnal frontal lobe epilepsy. A distinctive clinical disorderI E Scheffer, K P Bhatia, I Lopes-Cendes, et al.
Neurology|March 4, 1998
Pedigree analysis of French Canadian families with T14484C Leber's hereditary optic neuropathyC Macmillan, T Kirkham, K Fu, et al.
Neurology|March 23, 2007
Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3P Hedera, M A Blair, E Andermann, et al.
Lancet (London, England)|February 26, 1994
Autosomal dominant frontal epilepsy misdiagnosed as sleep disorderI E Scheffer, K P Bhatia, I Lopes-Cendes, et al.
American Journal of Human Genetics|January 1, 1996
The gene responsible for a severe form of peripheral neuropathy and agenesis of the corpus callosum maps to chromosome 15qL K Casaubon, M Melanson, I Lopes-Cendes, et al.
Neurology|November 18, 1998
Surgical treatment of epilepsy in tuberous sclerosis: strategies and results in 18 patientsM M Guerreiro, F Andermann, E Andermann, et al.
Pageof 16