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E Andermann

Showing results (21-30 of 159) with videos related to

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Genomics|May 1, 1994
Evidence for the existence of a fourth dominantly inherited spinocerebellar ataxia locusI Lopes-Cendes, E Andermann, G A Rouleau
Genetic Epidemiology|January 1, 1987
Pedigree discriminant analysis of two French Canadian Tay-Sachs familiesB J Keats, R C Elston, E Andermann
Clinical Genetics|May 1, 1989
The mutation mechanism causing juvenile-onset Tay-Sachs disease among LebaneseP Hechtman, B Boulay, J Bayleran, et al.
Neurology|March 4, 1998
Familial temporal lobe epilepsy: a clinically heterogeneous syndromeF Cendes, I Lopes-Cendes, E Andermann, et al.
Advances in Neurology|October 9, 1999
Cortical dysplasias, genetics, and epileptogenesisR Guerrini, E Andermann, M Avoli, et al.
Annals of Neurology|April 1, 1984
Juvenile progressive dystonia: a new phenotype of GM2 gangliosidosisD Meek, L S Wolfe, E Andermann, et al.
Metabolism: Clinical and Experimental|August 1, 1991
Glucose intolerance in first-degree relatives of patients with Friedreich's ataxia is associated with insulin resistance: evidence for a closely linked inherited traitI G Fantus, N Janjua, H Senni, et al.
Epilepsia|January 1, 1993
Progressive myoclonus epilepsies: clinical and genetic aspectsS F Berkovic, J Cochius, E Andermann, et al.
Neurology|June 1, 1987
Concepts of absence epilepsies: discrete syndromes or biological continuum?S F Berkovic, F Andermann, E Andermann, et al.
Human Genetics|April 1, 1992
The French Canadian Tay-Sachs disease deletion mutation: identification of probable foundersM De Braekeleer, P Hechtman, E Andermann, et al.
Pageof 16

Showing results (21-30 of 159) with videos related to

Sort By:
Pageof 16
Genomics|May 1, 1994
Evidence for the existence of a fourth dominantly inherited spinocerebellar ataxia locusI Lopes-Cendes, E Andermann, G A Rouleau
Genetic Epidemiology|January 1, 1987
Pedigree discriminant analysis of two French Canadian Tay-Sachs familiesB J Keats, R C Elston, E Andermann
Clinical Genetics|May 1, 1989
The mutation mechanism causing juvenile-onset Tay-Sachs disease among LebaneseP Hechtman, B Boulay, J Bayleran, et al.
Neurology|March 4, 1998
Familial temporal lobe epilepsy: a clinically heterogeneous syndromeF Cendes, I Lopes-Cendes, E Andermann, et al.
Advances in Neurology|October 9, 1999
Cortical dysplasias, genetics, and epileptogenesisR Guerrini, E Andermann, M Avoli, et al.
Annals of Neurology|April 1, 1984
Juvenile progressive dystonia: a new phenotype of GM2 gangliosidosisD Meek, L S Wolfe, E Andermann, et al.
Metabolism: Clinical and Experimental|August 1, 1991
Glucose intolerance in first-degree relatives of patients with Friedreich's ataxia is associated with insulin resistance: evidence for a closely linked inherited traitI G Fantus, N Janjua, H Senni, et al.
Epilepsia|January 1, 1993
Progressive myoclonus epilepsies: clinical and genetic aspectsS F Berkovic, J Cochius, E Andermann, et al.
Neurology|June 1, 1987
Concepts of absence epilepsies: discrete syndromes or biological continuum?S F Berkovic, F Andermann, E Andermann, et al.
Human Genetics|April 1, 1992
The French Canadian Tay-Sachs disease deletion mutation: identification of probable foundersM De Braekeleer, P Hechtman, E Andermann, et al.
Pageof 16