Search Results - Romina Combi
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Potassium Channels and Human Epileptic Phenotypes: An Updated Overview by Chiara Villa, Romina Combi
Published 2016Revisão -
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A rescuable folding defective Na<sub>v</sub>1.1 (<i>SCN1A</i>) sodium channel mutant causes GEFS+: Common mechanism in Na<sub>v</sub>1.1 related epilepsies? by Raffaella Rusconi, Romina Combi, Sandrine Cestèle, Daniele Grioni, Silvana Franceschetti, Leda DalprÃ, Massimo Mantegazza
Published 2009Artigo -
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Nocturnal Frontal Lobe Epilepsy by Lino Nobili, Paola Proserpio, Romina Combi, Federica Provini, Giuseppe Plazzi, Francesca Bisulli, Laura Tassi, Paolo Tinuper
Published 2014Revisão -
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<i>DEPDC5</i> mutations in families presenting as autosomal dominant nocturnal frontal lobe epilepsy by Fabienne Picard, Periklis Makrythanasis, Vincent Navarro, Saeko Ishida, Julitta de Bellescize, Dorothée Ville, Sarah Weckhuysen, Erwin Fosselle, Arvid Suls, Peter De Jonghe, Maryline Vasselon Raina, Gaëtan Lesca, Christel Depienne, Isabelle An-Gourfinkel, Mihaela Bustuchina ̆ Vlaicu, Michel Baulac, Emeline Mundwiller, Philippe Couarch, Romina Combi, Luigi Ferini‐Strambi, Antonio Gambardella, Stylianos E. Antonarakis, Eric LeGuern, Ortrud K. Steinlein, Stéphanie Baulac
Published 2014Artigo
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Biology
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Nocturnal
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Alzheimer's disease
Audiology
Cell biology
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Epileptogenesis
Focus (optics)
Folding (DSP implementation)
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Immunology
In vivo
Ion channel
Mechanism (biology)