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Neurology
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August 3, 2014
Genetic analysis of PHOX2B in sudden unexpected death in epilepsy cases
Richard D Bagnall, Douglas E Crompton, Carina Cutmore, et al.
American Journal of Medical Genetics. Part A
|
May 21, 2013
Deletions of 16p11.2 and 19p13.2 in a family with intellectual disability and generalized epilepsy
Alexander G Bassuk, Eileen Geraghty, Shu Wu, et al.
Epilepsia
|
January 14, 2017
De novo SCN1A pathogenic variants in the GEFS+ spectrum: Not always a familial syndrome
Kenneth A Myers, Rosemary Burgess, Zaid Afawi, et al.
Neurology
|
August 13, 2010
The core network in absence epilepsy. Differences in cortical and thalamic BOLD response
P W Carney, R A J Masterton, A S Harvey, et al.
Epilepsia
|
March 28, 2007
SCN2A mutations and benign familial neonatal-infantile seizures: the phenotypic spectrum
Eric Herlenius, Sarah E Heron, Bronwyn E Grinton, et al.
Archives of Neurology
|
May 10, 2006
Distinguishing sleep disorders from seizures: diagnosing bumps in the night
Christopher Paul Derry, Margot Davey, Murray Johns, et al.
Neurology
|
April 20, 2011
A distinctive seizure type in patients with CDKL5 mutations: Hypermotor-tonic-spasms sequence
K M Klein, S C Yendle, A S Harvey, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
January 14, 2020
Levetiracetam efficacy in PCDH19 Girls Clustering Epilepsy
Lynette G Sadleir, Kristy L Kolc, Chontelle King, et al.
Immunobiology
|
December 1, 1987
The course of Legionella pneumonia in guinea pigs after inhalation of various quantities of L. pneumophila
M J Twisk-Meijssen, P L Meenhorst, B J van Cronenburg, et al.
Epilepsia
|
February 28, 2006
Thalamic atrophy in childhood absence epilepsy
Chow Huat Patrick Chan, Regula S Briellmann, Gaby S Pell, et al.
Page
of 74
Search research articles
Search
Showing results (251-260 of 740) with videos related to
Sort By:
Page
of 74
Neurology
|
August 3, 2014
Genetic analysis of PHOX2B in sudden unexpected death in epilepsy cases
Richard D Bagnall, Douglas E Crompton, Carina Cutmore, et al.
American Journal of Medical Genetics. Part A
|
May 21, 2013
Deletions of 16p11.2 and 19p13.2 in a family with intellectual disability and generalized epilepsy
Alexander G Bassuk, Eileen Geraghty, Shu Wu, et al.
Epilepsia
|
January 14, 2017
De novo SCN1A pathogenic variants in the GEFS+ spectrum: Not always a familial syndrome
Kenneth A Myers, Rosemary Burgess, Zaid Afawi, et al.
Neurology
|
August 13, 2010
The core network in absence epilepsy. Differences in cortical and thalamic BOLD response
P W Carney, R A J Masterton, A S Harvey, et al.
Epilepsia
|
March 28, 2007
SCN2A mutations and benign familial neonatal-infantile seizures: the phenotypic spectrum
Eric Herlenius, Sarah E Heron, Bronwyn E Grinton, et al.
Archives of Neurology
|
May 10, 2006
Distinguishing sleep disorders from seizures: diagnosing bumps in the night
Christopher Paul Derry, Margot Davey, Murray Johns, et al.
Neurology
|
April 20, 2011
A distinctive seizure type in patients with CDKL5 mutations: Hypermotor-tonic-spasms sequence
K M Klein, S C Yendle, A S Harvey, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
January 14, 2020
Levetiracetam efficacy in PCDH19 Girls Clustering Epilepsy
Lynette G Sadleir, Kristy L Kolc, Chontelle King, et al.
Immunobiology
|
December 1, 1987
The course of Legionella pneumonia in guinea pigs after inhalation of various quantities of L. pneumophila
M J Twisk-Meijssen, P L Meenhorst, B J van Cronenburg, et al.
Epilepsia
|
February 28, 2006
Thalamic atrophy in childhood absence epilepsy
Chow Huat Patrick Chan, Regula S Briellmann, Gaby S Pell, et al.
Page
of 74