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Amedeo Bianchi

Showing results (11-20 of 33) with videos related to

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International Journal of Legal Medicine|August 15, 2014
Genetic and forensic implications in epilepsy and cardiac arrhythmias: a case seriesSara Partemi, Monica Coll Vidal, Pasquale Striano, et al.
Epilepsy Research|April 29, 2008
Autosomal dominant lateral temporal epilepsy: absence of mutations in ADAM22 and Kv1 channel genes encoding LGI1-associated proteinsErica Diani, Carlo Di Bonaventura, Oriano Mecarelli, et al.
Epilepsia|May 25, 2002
Lack of SCN1A mutations in familial febrile seizuresMichela Malacarne, Francesca Madia, Elena Gennaro, et al.
Neuroscience Letters|March 22, 2008
Analysis of LGI1 promoter sequence, PDYN and GABBR1 polymorphisms in sporadic and familial lateral temporal lobe epilepsyGiorgia Bovo, Erica Diani, Francesca Bisulli, 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|May 13, 2011
A functional polymorphism in the SCN1A gene does not influence antiepileptic drug responsiveness in Italian patients with focal epilepsyIda Manna, Antonio Gambardella, Amedeo Bianchi, 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|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.
Epilepsia|July 20, 2007
Mutational analysis of EFHC1 gene in Italian families with juvenile myoclonic epilepsyFerdinanda Annesi, Antonio Gambardella, Roberto Michelucci, et al.
Epilepsia|October 24, 2006
Exploration of the genetic architecture of idiopathic generalized epilepsiesAnne Hempelmann, Kirsten P Taylor, Armin Heils, et al.
Pageof 4

Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 4
International Journal of Legal Medicine|August 15, 2014
Genetic and forensic implications in epilepsy and cardiac arrhythmias: a case seriesSara Partemi, Monica Coll Vidal, Pasquale Striano, et al.
Epilepsy Research|April 29, 2008
Autosomal dominant lateral temporal epilepsy: absence of mutations in ADAM22 and Kv1 channel genes encoding LGI1-associated proteinsErica Diani, Carlo Di Bonaventura, Oriano Mecarelli, et al.
Epilepsia|May 25, 2002
Lack of SCN1A mutations in familial febrile seizuresMichela Malacarne, Francesca Madia, Elena Gennaro, et al.
Neuroscience Letters|March 22, 2008
Analysis of LGI1 promoter sequence, PDYN and GABBR1 polymorphisms in sporadic and familial lateral temporal lobe epilepsyGiorgia Bovo, Erica Diani, Francesca Bisulli, 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|May 13, 2011
A functional polymorphism in the SCN1A gene does not influence antiepileptic drug responsiveness in Italian patients with focal epilepsyIda Manna, Antonio Gambardella, Amedeo Bianchi, 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|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.
Epilepsia|July 20, 2007
Mutational analysis of EFHC1 gene in Italian families with juvenile myoclonic epilepsyFerdinanda Annesi, Antonio Gambardella, Roberto Michelucci, et al.
Epilepsia|October 24, 2006
Exploration of the genetic architecture of idiopathic generalized epilepsiesAnne Hempelmann, Kirsten P Taylor, Armin Heils, et al.
Pageof 4