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Frederick Andermann

Showing results (91-100 of 115) with videos related to

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Epileptic Disorders : International Epilepsy Journal with Videotape|June 24, 2006
Are epilepsy classifications based on epileptic syndromes and seizure types outdated?Jerome Engel, Anne Berg, Frederick Andermann, et al.
Annals of Neurology|January 2, 2003
An ALS2 gene mutation causes hereditary spastic paraplegia in a Pakistani kindredFrançois Gros-Louis, Inge A Meijer, Collette K Hand, et al.
Epilepsia|March 10, 2007
Seizure outcome after resection of supratentorial cavernous malformations: a study of 168 patientsChristian R Baumann, Nicola Acciarri, Helmut Bertalanffy, et al.
Brain : a Journal of Neurology|September 15, 2004
Action myoclonus-renal failure syndrome: characterization of a unique cerebro-renal disorderAmanPreet Badhwar, Samuel F Berkovic, John P Dowling, et al.
European Journal of Human Genetics : EJHG|January 11, 2020
Autosomal-dominant adult neuronal ceroid lipofuscinosis caused by duplication in DNAJC5 initially missed by Sanger and whole-exome sequencingIvana Jedličková, Maxime Cadieux-Dion, Anna Přistoupilová, et al.
Brain : a Journal of Neurology|April 21, 2010
Clinical and imaging heterogeneity of polymicrogyria: a study of 328 patientsRichard J Leventer, Anna Jansen, Daniela T Pilz, et al.
Annals of Neurology|January 28, 2015
Familial focal epilepsy with focal cortical dysplasia due to DEPDC5 mutationsStéphanie Baulac, Saeko Ishida, Elise Marsan, et al.
Neurology|August 24, 2012
Peritrigonal and temporo-occipital heterotopia with corpus callosum and cerebellar dysgenesisTiziana Pisano, A James Barkovich, Richard J Leventer, et al.
Annals of Neurology|July 3, 2003
Nonsyndromic mental retardation and cryptogenic epilepsy in women with doublecortin gene mutationsRenzo Guerrini, Francesca Moro, Eva Andermann, et al.
Epilepsia|August 27, 2004
Familial partial epilepsy with variable foci: clinical features and linkage to chromosome 22q12Samuel F Berkovic, Jose M Serratosa, Hilary A Phillips, et al.
Pageof 12

Showing results (91-100 of 115) with videos related to

Sort By:
Pageof 12
Epileptic Disorders : International Epilepsy Journal with Videotape|June 24, 2006
Are epilepsy classifications based on epileptic syndromes and seizure types outdated?Jerome Engel, Anne Berg, Frederick Andermann, et al.
Annals of Neurology|January 2, 2003
An ALS2 gene mutation causes hereditary spastic paraplegia in a Pakistani kindredFrançois Gros-Louis, Inge A Meijer, Collette K Hand, et al.
Epilepsia|March 10, 2007
Seizure outcome after resection of supratentorial cavernous malformations: a study of 168 patientsChristian R Baumann, Nicola Acciarri, Helmut Bertalanffy, et al.
Brain : a Journal of Neurology|September 15, 2004
Action myoclonus-renal failure syndrome: characterization of a unique cerebro-renal disorderAmanPreet Badhwar, Samuel F Berkovic, John P Dowling, et al.
European Journal of Human Genetics : EJHG|January 11, 2020
Autosomal-dominant adult neuronal ceroid lipofuscinosis caused by duplication in DNAJC5 initially missed by Sanger and whole-exome sequencingIvana Jedličková, Maxime Cadieux-Dion, Anna Přistoupilová, et al.
Brain : a Journal of Neurology|April 21, 2010
Clinical and imaging heterogeneity of polymicrogyria: a study of 328 patientsRichard J Leventer, Anna Jansen, Daniela T Pilz, et al.
Annals of Neurology|January 28, 2015
Familial focal epilepsy with focal cortical dysplasia due to DEPDC5 mutationsStéphanie Baulac, Saeko Ishida, Elise Marsan, et al.
Neurology|August 24, 2012
Peritrigonal and temporo-occipital heterotopia with corpus callosum and cerebellar dysgenesisTiziana Pisano, A James Barkovich, Richard J Leventer, et al.
Annals of Neurology|July 3, 2003
Nonsyndromic mental retardation and cryptogenic epilepsy in women with doublecortin gene mutationsRenzo Guerrini, Francesca Moro, Eva Andermann, et al.
Epilepsia|August 27, 2004
Familial partial epilepsy with variable foci: clinical features and linkage to chromosome 22q12Samuel F Berkovic, Jose M Serratosa, Hilary A Phillips, et al.
Pageof 12