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Elena Gennaro

Showing results (21-30 of 37) with videos related to

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Seizure|January 28, 2019
Chewing induced reflex seizures ("eating epilepsy") and eye closure sensitivity as a common feature in pediatric patients with SYNGAP1 mutations: Review of literature and report of 8 casesCelina von Stülpnagel, Till Hartlieb, Ingo Borggräfe, et al.
Epilepsia|March 15, 2006
Clinical and genetic findings in 26 Italian patients with Lafora diseaseSilvana Franceschetti, Antonio Gambardella, Laura Canafoglia, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|August 17, 2018
Early Treatment with Quinidine in 2 Patients with Epilepsy of Infancy with Migrating Focal Seizures (EIMFS) Due to Gain-of-Function KCNT1 Mutations: Functional Studies, Clinical Responses, and Critical Issues for Personalized TherapyRobertino Dilena, Jacopo C DiFrancesco, Maria Virginia Soldovieri, et al.
Epilepsia|October 2, 2014
Mild Lafora disease: clinical, neurophysiologic, and genetic findingsEdoardo Ferlazzo, Laura Canafoglia, Roberto Michelucci, et al.
Epilepsia|May 25, 2002
Lack of SCN1A mutations in familial febrile seizuresMichela Malacarne, Francesca Madia, Elena Gennaro, et al.
Epilepsy Research|April 16, 2003
No evidence of GABRG2 mutations in severe myoclonic epilepsy of infancyFrancesca Madia, Elena Gennaro, Massimiliano Cecconi, et al.
Epilepsia|October 24, 2006
Familial occurrence of febrile seizures and epilepsy in severe myoclonic epilepsy of infancy (SMEI) patients with SCN1A mutationsMaria Margherita Mancardi, Pasquale Striano, Elena Gennaro, et al.
American Journal of Medical Genetics|September 5, 2002
No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 18q21.1Thomas Sander, Christine Windemuth, Herbert Schulz, et al.
Epilepsia|July 11, 2006
Linkage analysis and disease models in benign familial infantile seizures: a study of 16 familiesPasquale Striano, Maria Luisa Lispi, Elena Gennaro, et al.
Epilepsia|April 30, 2009
SCN1A duplications and deletions detected in Dravet syndrome: implications for molecular diagnosisCarla Marini, Ingrid E Scheffer, Rima Nabbout, et al.
Pageof 4

Showing results (21-30 of 37) with videos related to

Sort By:
Pageof 4
Seizure|January 28, 2019
Chewing induced reflex seizures ("eating epilepsy") and eye closure sensitivity as a common feature in pediatric patients with SYNGAP1 mutations: Review of literature and report of 8 casesCelina von Stülpnagel, Till Hartlieb, Ingo Borggräfe, et al.
Epilepsia|March 15, 2006
Clinical and genetic findings in 26 Italian patients with Lafora diseaseSilvana Franceschetti, Antonio Gambardella, Laura Canafoglia, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|August 17, 2018
Early Treatment with Quinidine in 2 Patients with Epilepsy of Infancy with Migrating Focal Seizures (EIMFS) Due to Gain-of-Function KCNT1 Mutations: Functional Studies, Clinical Responses, and Critical Issues for Personalized TherapyRobertino Dilena, Jacopo C DiFrancesco, Maria Virginia Soldovieri, et al.
Epilepsia|October 2, 2014
Mild Lafora disease: clinical, neurophysiologic, and genetic findingsEdoardo Ferlazzo, Laura Canafoglia, Roberto Michelucci, et al.
Epilepsia|May 25, 2002
Lack of SCN1A mutations in familial febrile seizuresMichela Malacarne, Francesca Madia, Elena Gennaro, et al.
Epilepsy Research|April 16, 2003
No evidence of GABRG2 mutations in severe myoclonic epilepsy of infancyFrancesca Madia, Elena Gennaro, Massimiliano Cecconi, et al.
Epilepsia|October 24, 2006
Familial occurrence of febrile seizures and epilepsy in severe myoclonic epilepsy of infancy (SMEI) patients with SCN1A mutationsMaria Margherita Mancardi, Pasquale Striano, Elena Gennaro, et al.
American Journal of Medical Genetics|September 5, 2002
No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 18q21.1Thomas Sander, Christine Windemuth, Herbert Schulz, et al.
Epilepsia|July 11, 2006
Linkage analysis and disease models in benign familial infantile seizures: a study of 16 familiesPasquale Striano, Maria Luisa Lispi, Elena Gennaro, et al.
Epilepsia|April 30, 2009
SCN1A duplications and deletions detected in Dravet syndrome: implications for molecular diagnosisCarla Marini, Ingrid E Scheffer, Rima Nabbout, et al.
Pageof 4