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E Andermann

Showing results (131-140 of 159) with videos related to

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Epilepsia|August 8, 2001
Severe myoclonic epilepsy of infancy: extended spectrum of GEFS+?R Singh, E Andermann, W P Whitehouse, et al.
Journal of Medical Genetics|September 10, 2003
Genetic mapping of a new Lafora progressive myoclonus epilepsy locus (EPM2B) on 6p22E M Chan, D E Bulman, A D Paterson, et al.
Human Molecular Genetics|August 1, 1997
The Friedreich ataxia GAA triplet repeat: premutation and normal allelesL Montermini, E Andermann, M Labuda, et al.
Neuropediatrics|February 1, 1997
Genetic linkage analysis of a variant of juvenile onset neuronal ceroid lipofuscinosis with granular osmiophilic depositsA O'Rawe, H M Mitchison, R Williams, et al.
Genomics|December 15, 1996
Isolation and characterization of GT335, a novel human gene conserved in Escherichia coli and mapping to 21q22.3R G Lafrenière, D L Rochefort, Z Kibar, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 18, 2006
Patterns of hippocampal abnormalities in malformations of cortical developmentM A Montenegro, D Kinay, F Cendes, et al.
Neurology|June 24, 2004
Posterior quadrantic dysplasia or hemi-hemimegalencephaly: a characteristic brain malformationM D D'Agostino, A Bastos, C Piras, et al.
Clinical Genetics|September 18, 2012
Recurrent mutations in DNAJC5 cause autosomal dominant Kufs diseaseM Cadieux-Dion, E Andermann, P Lachance-Touchette, et al.
American Journal of Human Genetics|December 1, 1999
Mapping of a gene determining familial partial epilepsy with variable foci to chromosome 22q11-q12L Xiong, M Labuda, D S Li, et al.
Neurology|September 25, 2003
Sodium channel alpha1-subunit mutations in severe myoclonic epilepsy of infancy and infantile spasmsR H Wallace, B L Hodgson, B E Grinton, et al.
Pageof 16

Showing results (131-140 of 159) with videos related to

Sort By:
Pageof 16
Epilepsia|August 8, 2001
Severe myoclonic epilepsy of infancy: extended spectrum of GEFS+?R Singh, E Andermann, W P Whitehouse, et al.
Journal of Medical Genetics|September 10, 2003
Genetic mapping of a new Lafora progressive myoclonus epilepsy locus (EPM2B) on 6p22E M Chan, D E Bulman, A D Paterson, et al.
Human Molecular Genetics|August 1, 1997
The Friedreich ataxia GAA triplet repeat: premutation and normal allelesL Montermini, E Andermann, M Labuda, et al.
Neuropediatrics|February 1, 1997
Genetic linkage analysis of a variant of juvenile onset neuronal ceroid lipofuscinosis with granular osmiophilic depositsA O'Rawe, H M Mitchison, R Williams, et al.
Genomics|December 15, 1996
Isolation and characterization of GT335, a novel human gene conserved in Escherichia coli and mapping to 21q22.3R G Lafrenière, D L Rochefort, Z Kibar, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 18, 2006
Patterns of hippocampal abnormalities in malformations of cortical developmentM A Montenegro, D Kinay, F Cendes, et al.
Neurology|June 24, 2004
Posterior quadrantic dysplasia or hemi-hemimegalencephaly: a characteristic brain malformationM D D'Agostino, A Bastos, C Piras, et al.
Clinical Genetics|September 18, 2012
Recurrent mutations in DNAJC5 cause autosomal dominant Kufs diseaseM Cadieux-Dion, E Andermann, P Lachance-Touchette, et al.
American Journal of Human Genetics|December 1, 1999
Mapping of a gene determining familial partial epilepsy with variable foci to chromosome 22q11-q12L Xiong, M Labuda, D S Li, et al.
Neurology|September 25, 2003
Sodium channel alpha1-subunit mutations in severe myoclonic epilepsy of infancy and infantile spasmsR H Wallace, B L Hodgson, B E Grinton, et al.
Pageof 16