Search research articles
Contact Us
Filters
Showing results (21-30 of 70) with videos related to
Page
of 7
Sort By:
Brain : a Journal of Neurology
|
November 29, 2005
Periventricular nodular heterotopia with overlying polymicrogyria
Gretchen Wieck, Richard J Leventer, Waney M Squier, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 8, 2006
Developments in neuroacanthocytosis: expanding the spectrum of choreatic syndromes
Ruth H Walker, Adrian Danek, Carol Dobson-Stone, et al.
Epilepsia
|
July 6, 2018
Evidence of linkage to chromosome 5p13.2-q11.1 in a large inbred family with genetic generalized epilepsy
Demet Kinay, Karen L Oliver, Erdem Tüzün, et al.
Epilepsy Research
|
January 22, 2003
alpha-[11C]-Methyl-L-tryptophan PET identifies the epileptogenic tuber and correlates with interictal spike frequency
Marco Fedi, David C Reutens, Frederick Andermann, et al.
Brain : a Journal of Neurology
|
January 23, 2004
Differential impact of the FMR1 gene on visual processing in fragile X syndrome
Cary S Kogan, Isabelle Boutet, Kim Cornish, et al.
American Journal of Medical Genetics. Part A
|
October 30, 2019
Duplication 2p16 is associated with perisylvian polymicrogyria
Dina Amrom, Annapurna Poduri, Jennifer S Goldman, et al.
Epilepsia
|
December 16, 2015
Brivaracetam in Unverricht-Lundborg disease (EPM1): Results from two randomized, double-blind, placebo-controlled studies
Reetta Kälviäinen, Pierre Genton, Eva Andermann, et al.
Epilepsia
|
July 31, 2003
Outcome of surgical treatment in familial mesial temporal lobe epilepsy
Eliane Kobayashi, Maria Daniela D'Agostino, Iscia Lopes-Cendes, et al.
Epilepsia
|
August 3, 2005
Familial temporal lobe epilepsy as a presenting feature of choreoacanthocytosis
Abdullah Al-Asmi, An C Jansen, AmanPreet Badhwar, et al.
Archives of Neurology
|
November 14, 2007
Sanfilippo syndrome type D: natural history and identification of 3 novel mutations in the GNS Gene
An C M Jansen, Henian Cao, Paige Kaplan, et al.
Page
of 7
Search research articles
Search
Showing results (21-30 of 70) with videos related to
Sort By:
Page
of 7
Brain : a Journal of Neurology
|
November 29, 2005
Periventricular nodular heterotopia with overlying polymicrogyria
Gretchen Wieck, Richard J Leventer, Waney M Squier, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 8, 2006
Developments in neuroacanthocytosis: expanding the spectrum of choreatic syndromes
Ruth H Walker, Adrian Danek, Carol Dobson-Stone, et al.
Epilepsia
|
July 6, 2018
Evidence of linkage to chromosome 5p13.2-q11.1 in a large inbred family with genetic generalized epilepsy
Demet Kinay, Karen L Oliver, Erdem Tüzün, et al.
Epilepsy Research
|
January 22, 2003
alpha-[11C]-Methyl-L-tryptophan PET identifies the epileptogenic tuber and correlates with interictal spike frequency
Marco Fedi, David C Reutens, Frederick Andermann, et al.
Brain : a Journal of Neurology
|
January 23, 2004
Differential impact of the FMR1 gene on visual processing in fragile X syndrome
Cary S Kogan, Isabelle Boutet, Kim Cornish, et al.
American Journal of Medical Genetics. Part A
|
October 30, 2019
Duplication 2p16 is associated with perisylvian polymicrogyria
Dina Amrom, Annapurna Poduri, Jennifer S Goldman, et al.
Epilepsia
|
December 16, 2015
Brivaracetam in Unverricht-Lundborg disease (EPM1): Results from two randomized, double-blind, placebo-controlled studies
Reetta Kälviäinen, Pierre Genton, Eva Andermann, et al.
Epilepsia
|
July 31, 2003
Outcome of surgical treatment in familial mesial temporal lobe epilepsy
Eliane Kobayashi, Maria Daniela D'Agostino, Iscia Lopes-Cendes, et al.
Epilepsia
|
August 3, 2005
Familial temporal lobe epilepsy as a presenting feature of choreoacanthocytosis
Abdullah Al-Asmi, An C Jansen, AmanPreet Badhwar, et al.
Archives of Neurology
|
November 14, 2007
Sanfilippo syndrome type D: natural history and identification of 3 novel mutations in the GNS Gene
An C M Jansen, Henian Cao, Paige Kaplan, et al.
Page
of 7