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E Andermann

Showing results (101-110 of 159) with videos related to

Pageof 16
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Neurology|February 13, 2003
Hippocampal atrophy and T2-weighted signal changes in familial mesial temporal lobe epilepsyE Kobayashi, M D D'Agostino, I Lopes-Cendes, et al.
Neurology|April 14, 2004
CCM1 mutation screen of sporadic cases with cerebral cavernous malformationsD J Verlaan, S B Laurent, U Sure, et al.
Neurology|June 1, 1988
Excitatory amino acids are elevated in human epileptic cerebral cortexA Sherwin, Y Robitaille, F Quesney, et al.
American Journal of Human Genetics|May 1, 1985
Folic acid blinded trial in identical twins with fragile X syndromeD S Rosenblatt, E A Duschenes, F V Hellstrom, et al.
Neurology|June 1, 1997
Band heterotopia or double cortex in a male: bridging structures suggest abnormality of the radial glial guide systemJ Ono, T Mano, E Andermann, et al.
American Journal of Human Genetics|May 1, 1994
Confirmation of the SCA-2 locus as an alternative locus for dominantly inherited spinocerebellar ataxias and refinement of the candidate regionI Lopes-Cendes, E Andermann, E Attig, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|May 1, 1982
Increased plasma catecholamines in patients with Friedreich's ataxiaA Pasternac, P Wagniart, R Olivenstein, et al.
Neurology|April 14, 2004
Epilepsy in twins: insights from unique historical data of William LennoxL Vadlamudi, E Andermann, C T Lombroso, et al.
Brain : a Journal of Neurology|October 1, 1995
Periventricular and subcortical nodular heterotopia. A study of 33 patientsF Dubeau, D Tampieri, N Lee, et al.
Neurology|February 5, 1999
Periventricular leukomalacia and epilepsy: incidence and seizure patternC Gurses, D W Gross, F Andermann, et al.
Pageof 16

Showing results (101-110 of 159) with videos related to

Sort By:
Pageof 16
Neurology|February 13, 2003
Hippocampal atrophy and T2-weighted signal changes in familial mesial temporal lobe epilepsyE Kobayashi, M D D'Agostino, I Lopes-Cendes, et al.
Neurology|April 14, 2004
CCM1 mutation screen of sporadic cases with cerebral cavernous malformationsD J Verlaan, S B Laurent, U Sure, et al.
Neurology|June 1, 1988
Excitatory amino acids are elevated in human epileptic cerebral cortexA Sherwin, Y Robitaille, F Quesney, et al.
American Journal of Human Genetics|May 1, 1985
Folic acid blinded trial in identical twins with fragile X syndromeD S Rosenblatt, E A Duschenes, F V Hellstrom, et al.
Neurology|June 1, 1997
Band heterotopia or double cortex in a male: bridging structures suggest abnormality of the radial glial guide systemJ Ono, T Mano, E Andermann, et al.
American Journal of Human Genetics|May 1, 1994
Confirmation of the SCA-2 locus as an alternative locus for dominantly inherited spinocerebellar ataxias and refinement of the candidate regionI Lopes-Cendes, E Andermann, E Attig, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|May 1, 1982
Increased plasma catecholamines in patients with Friedreich's ataxiaA Pasternac, P Wagniart, R Olivenstein, et al.
Neurology|April 14, 2004
Epilepsy in twins: insights from unique historical data of William LennoxL Vadlamudi, E Andermann, C T Lombroso, et al.
Brain : a Journal of Neurology|October 1, 1995
Periventricular and subcortical nodular heterotopia. A study of 33 patientsF Dubeau, D Tampieri, N Lee, et al.
Neurology|February 5, 1999
Periventricular leukomalacia and epilepsy: incidence and seizure patternC Gurses, D W Gross, F Andermann, et al.
Pageof 16