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Davide Mei

Showing results (11-20 of 110) with videos related to

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Epilepsy Research|November 11, 2011
Early clinical features in Dravet syndrome patients with and without SCN1A mutationsCristina Petrelli, Claudia Passamonti, Elisabetta Cesaroni, et al.
Cephalalgia : an International Journal of Headache|July 11, 2013
Functional characterization of a novel C-terminal ATP1A2 mutation causing hemiplegic migraine and epilepsyTiziana Pisano, Susan Spiller, Davide Mei, et al.
Epilepsy & Behavior : E&B|January 9, 2015
A novel inherited SCN1A mutation associated with different neuropsychological phenotypes: is there a common core deficit?Claudia Passamonti, Cristina Petrelli, Davide Mei, et al.
American Journal of Medical Genetics. Part A|April 13, 2011
In-frame deletion in FLNA causing familial periventricular heterotopia with skeletal dysplasia in malesElena Parrini, Isabel Llano Rivas, Joaquin Fernandez Toral, et al.
Epilepsia|January 6, 2011
Variable epilepsy phenotypes associated with a familial intragenic deletion of the SCN1A geneRenzo Guerrini, Elena Cellini, Davide Mei, et al.
Epilepsia|August 24, 2010
Familial Lennox-Gastaut syndrome in male siblings with a novel DCX mutation and anterior pachygyriaKate M Lawrence, Davide Mei, Mark R Newton, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|June 18, 2013
Clinical and polygraphic study of familial paroxysmal kinesigenic dyskinesia with PRRT2 mutationMargherita Fabbri, Carla Marini, Francesca Bisulli, et al.
Developmental Medicine and Child Neurology|February 12, 2011
CDKL5 gene-related epileptic encephalopathy: electroclinical findings in the first year of lifeFederico Melani, Davide Mei, Tiziana Pisano, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|August 31, 2012
Semiological study of ictal affective behaviour in epilepsy and mental retardation limited to females (EFMR)Elena Antelmi, Massimo Mastrangelo, Francesca Bisulli, et al.
Neurobiology of Disease|October 17, 2012
Impaired surface αβγ GABA(A) receptor expression in familial epilepsy due to a GABRG2 frameshift mutationMengnan Tian, Davide Mei, Elena Freri, et al.
Pageof 11

Showing results (11-20 of 110) with videos related to

Sort By:
Pageof 11
Epilepsy Research|November 11, 2011
Early clinical features in Dravet syndrome patients with and without SCN1A mutationsCristina Petrelli, Claudia Passamonti, Elisabetta Cesaroni, et al.
Cephalalgia : an International Journal of Headache|July 11, 2013
Functional characterization of a novel C-terminal ATP1A2 mutation causing hemiplegic migraine and epilepsyTiziana Pisano, Susan Spiller, Davide Mei, et al.
Epilepsy & Behavior : E&B|January 9, 2015
A novel inherited SCN1A mutation associated with different neuropsychological phenotypes: is there a common core deficit?Claudia Passamonti, Cristina Petrelli, Davide Mei, et al.
American Journal of Medical Genetics. Part A|April 13, 2011
In-frame deletion in FLNA causing familial periventricular heterotopia with skeletal dysplasia in malesElena Parrini, Isabel Llano Rivas, Joaquin Fernandez Toral, et al.
Epilepsia|January 6, 2011
Variable epilepsy phenotypes associated with a familial intragenic deletion of the SCN1A geneRenzo Guerrini, Elena Cellini, Davide Mei, et al.
Epilepsia|August 24, 2010
Familial Lennox-Gastaut syndrome in male siblings with a novel DCX mutation and anterior pachygyriaKate M Lawrence, Davide Mei, Mark R Newton, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|June 18, 2013
Clinical and polygraphic study of familial paroxysmal kinesigenic dyskinesia with PRRT2 mutationMargherita Fabbri, Carla Marini, Francesca Bisulli, et al.
Developmental Medicine and Child Neurology|February 12, 2011
CDKL5 gene-related epileptic encephalopathy: electroclinical findings in the first year of lifeFederico Melani, Davide Mei, Tiziana Pisano, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|August 31, 2012
Semiological study of ictal affective behaviour in epilepsy and mental retardation limited to females (EFMR)Elena Antelmi, Massimo Mastrangelo, Francesca Bisulli, et al.
Neurobiology of Disease|October 17, 2012
Impaired surface αβγ GABA(A) receptor expression in familial epilepsy due to a GABRG2 frameshift mutationMengnan Tian, Davide Mei, Elena Freri, et al.
Pageof 11