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Romina Combi

Showing results (31-40 of 36) with videos related to

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Journal of Neurology|August 27, 2002
Exclusion of linkage of nine neuronal nicotinic acetylcholine receptor subunit genes expressed in brain in autosomal dominant nocturnal frontal lobe epilepsy in four unrelated familiesMaria Teresa Bonati, Romina Combi, Rosanna Asselta, et al.
Seizure|March 24, 2019
Migrating focal seizures in Autosomal Dominant Sleep-related Hypermotor Epilepsy with KCNT1 mutationMatteo Cataldi, Lino Nobili, Federico Zara, et al.
Brain Research Bulletin|February 10, 2009
Clinical and genetic familial study of a large cohort of Italian children with idiopathic epilepsyRomina Combi, Daniele Grioni, Margherita Contri, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|June 16, 2020
Variants in <i>CHRNB2</i> and <i>CHRNA4</i> Identified in Patients with Insular EpilepsyMaxime Cadieux-Dion, Simone Meneghini, Chiara Villa, et al.
Free Radical Biology & Medicine|April 9, 2017
Simultaneous overexpression of human E5NT and ENTPD1 protects porcine endothelial cells against H<sub>2</sub>O<sub>2</sub>-induced oxidative stress and cytotoxicity in vitroElisa Chisci, Marco De Giorgi, Elisa Zanfrini, et al.
Neurology|May 13, 2014
DEPDC5 mutations in families presenting as autosomal dominant nocturnal frontal lobe epilepsyFabienne Picard, Periklis Makrythanasis, Vincent Navarro, et al.
Pageof 4

Showing results (31-40 of 36) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 36 results.
Journal of Neurology|August 27, 2002
Exclusion of linkage of nine neuronal nicotinic acetylcholine receptor subunit genes expressed in brain in autosomal dominant nocturnal frontal lobe epilepsy in four unrelated familiesMaria Teresa Bonati, Romina Combi, Rosanna Asselta, et al.
Seizure|March 24, 2019
Migrating focal seizures in Autosomal Dominant Sleep-related Hypermotor Epilepsy with KCNT1 mutationMatteo Cataldi, Lino Nobili, Federico Zara, et al.
Brain Research Bulletin|February 10, 2009
Clinical and genetic familial study of a large cohort of Italian children with idiopathic epilepsyRomina Combi, Daniele Grioni, Margherita Contri, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|June 16, 2020
Variants in <i>CHRNB2</i> and <i>CHRNA4</i> Identified in Patients with Insular EpilepsyMaxime Cadieux-Dion, Simone Meneghini, Chiara Villa, et al.
Free Radical Biology & Medicine|April 9, 2017
Simultaneous overexpression of human E5NT and ENTPD1 protects porcine endothelial cells against H<sub>2</sub>O<sub>2</sub>-induced oxidative stress and cytotoxicity in vitroElisa Chisci, Marco De Giorgi, Elisa Zanfrini, et al.
Neurology|May 13, 2014
DEPDC5 mutations in families presenting as autosomal dominant nocturnal frontal lobe epilepsyFabienne Picard, Periklis Makrythanasis, Vincent Navarro, et al.
Pageof 4