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Showing results (251-260 of 740) with videos related to

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Neurology|August 3, 2014
Genetic analysis of PHOX2B in sudden unexpected death in epilepsy casesRichard 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 epilepsyAlexander 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 syndromeKenneth A Myers, Rosemary Burgess, Zaid Afawi, et al.
Neurology|August 13, 2010
The core network in absence epilepsy. Differences in cortical and thalamic BOLD responseP 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 spectrumEric Herlenius, Sarah E Heron, Bronwyn E Grinton, et al.
Archives of Neurology|May 10, 2006
Distinguishing sleep disorders from seizures: diagnosing bumps in the nightChristopher Paul Derry, Margot Davey, Murray Johns, et al.
Neurology|April 20, 2011
A distinctive seizure type in patients with CDKL5 mutations: Hypermotor-tonic-spasms sequenceK 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 EpilepsyLynette 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. pneumophilaM J Twisk-Meijssen, P L Meenhorst, B J van Cronenburg, et al.
Epilepsia|February 28, 2006
Thalamic atrophy in childhood absence epilepsyChow Huat Patrick Chan, Regula S Briellmann, Gaby S Pell, et al.
Pageof 74

Showing results (251-260 of 740) with videos related to

Sort By:
Pageof 74
Neurology|August 3, 2014
Genetic analysis of PHOX2B in sudden unexpected death in epilepsy casesRichard 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 epilepsyAlexander 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 syndromeKenneth A Myers, Rosemary Burgess, Zaid Afawi, et al.
Neurology|August 13, 2010
The core network in absence epilepsy. Differences in cortical and thalamic BOLD responseP 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 spectrumEric Herlenius, Sarah E Heron, Bronwyn E Grinton, et al.
Archives of Neurology|May 10, 2006
Distinguishing sleep disorders from seizures: diagnosing bumps in the nightChristopher Paul Derry, Margot Davey, Murray Johns, et al.
Neurology|April 20, 2011
A distinctive seizure type in patients with CDKL5 mutations: Hypermotor-tonic-spasms sequenceK 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 EpilepsyLynette 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. pneumophilaM J Twisk-Meijssen, P L Meenhorst, B J van Cronenburg, et al.
Epilepsia|February 28, 2006
Thalamic atrophy in childhood absence epilepsyChow Huat Patrick Chan, Regula S Briellmann, Gaby S Pell, et al.
Pageof 74