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E Andermann

Showing results (141-150 of 159) with videos related to

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Neurology|August 1, 1996
X-linked malformations of neuronal migrationW B Dobyns, E Andermann, F Andermann, et al.
Annals of Neurology|October 23, 2009
SCARB2 mutations in progressive myoclonus epilepsy (PME) without renal failureL M Dibbens, R Michelucci, A Gambardella, et al.
Acta Neurologica Scandinavica|January 6, 1999
Anticipation in familial cavernous angioma: ascertainment bias or genetic causeA M Siegel, F Andermann, A Badhwar, et al.
Der Nervenarzt|February 11, 2005
[Familial cavernous malformations of the central nervous system. A clinical and genetic study of 15 German families]A M Siegel, H Bertalanffy, J J Dichgans, et al.
Neurology|May 20, 2009
SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophyM C Hannibal, E K Ruzzo, L R Miller, et al.
American Journal of Human Genetics|October 3, 1998
Autosomal dominant nocturnal frontal-lobe epilepsy: genetic heterogeneity and evidence for a second locus at 15q24H A Phillips, I E Scheffer, K M Crossland, et al.
Annals of Neurology|May 1, 1997
Phenotypic variability in Friedreich ataxia: role of the associated GAA triplet repeat expansionL Montermini, A Richter, K Morgan, et al.
Epilepsia|October 3, 2001
Surgical resection for intractable epilepsy in "double cortex" syndrome yields inadequate resultsA Bernasconi, V Martinez, P Rosa-Neto, et al.
Epilepsy Research|March 27, 1999
Congenital malformations due to antiepileptic drugsS Kaneko, D Battino, E Andermann, et al.
Human Molecular Genetics|March 21, 1998
Mutations in the palmitoyl-protein thioesterase gene (PPT; CLN1) causing juvenile neuronal ceroid lipofuscinosis with granular osmiophilic depositsH M Mitchison, S L Hofmann, C H Becerra, et al.
Pageof 16

Showing results (141-150 of 159) with videos related to

Sort By:
Pageof 16
Neurology|August 1, 1996
X-linked malformations of neuronal migrationW B Dobyns, E Andermann, F Andermann, et al.
Annals of Neurology|October 23, 2009
SCARB2 mutations in progressive myoclonus epilepsy (PME) without renal failureL M Dibbens, R Michelucci, A Gambardella, et al.
Acta Neurologica Scandinavica|January 6, 1999
Anticipation in familial cavernous angioma: ascertainment bias or genetic causeA M Siegel, F Andermann, A Badhwar, et al.
Der Nervenarzt|February 11, 2005
[Familial cavernous malformations of the central nervous system. A clinical and genetic study of 15 German families]A M Siegel, H Bertalanffy, J J Dichgans, et al.
Neurology|May 20, 2009
SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophyM C Hannibal, E K Ruzzo, L R Miller, et al.
American Journal of Human Genetics|October 3, 1998
Autosomal dominant nocturnal frontal-lobe epilepsy: genetic heterogeneity and evidence for a second locus at 15q24H A Phillips, I E Scheffer, K M Crossland, et al.
Annals of Neurology|May 1, 1997
Phenotypic variability in Friedreich ataxia: role of the associated GAA triplet repeat expansionL Montermini, A Richter, K Morgan, et al.
Epilepsia|October 3, 2001
Surgical resection for intractable epilepsy in "double cortex" syndrome yields inadequate resultsA Bernasconi, V Martinez, P Rosa-Neto, et al.
Epilepsy Research|March 27, 1999
Congenital malformations due to antiepileptic drugsS Kaneko, D Battino, E Andermann, et al.
Human Molecular Genetics|March 21, 1998
Mutations in the palmitoyl-protein thioesterase gene (PPT; CLN1) causing juvenile neuronal ceroid lipofuscinosis with granular osmiophilic depositsH M Mitchison, S L Hofmann, C H Becerra, et al.
Pageof 16