Výsledky vyhledávání - Raffaella Rusconi
- Zobrazuji výsledky 1 - 16 z 16
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Self-Limited Hyperexcitability: Functional Effect of a Familial Hemiplegic Migraine Mutation of the Na<sub>v</sub>1.1 (SCN1A) Na<sup>+</sup>Channel Autor Sandrine Cestèle, Paolo Scalmani, Raffaella Rusconi, Benedetta Terragni, Silvana Franceschetti, Massimo Mantegazza
Vydáno 2008Artigo -
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Effects in Neocortical Neurons of Mutations of the Na<sub>v</sub>1.2 Na<sup>+</sup>Channel causing Benign Familial Neonatal-Infantile Seizures Autor Paolo Scalmani, Raffaella Rusconi, Elena Armatura, Federico Zara, G. Avanzini, Silvana Franceschetti, Massimo Mantegazza
Vydáno 2006Artigo -
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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? Autor Raffaella Rusconi, Romina Combi, Sandrine Cestèle, Daniele Grioni, Silvana Franceschetti, Leda DalprÃ, Massimo Mantegazza
Vydáno 2009Artigo -
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Divergent effects of the <scp>T</scp>1174S <scp><i>SCN1A</i></scp> mutation associated with seizures and hemiplegic migraine Autor Sandrine Cestèle, Angelo Labate, Raffaella Rusconi, Patrizia Tarantino, Laura Mumoli, Silvana Franceschetti, Grazia Annesi, Massimo Mantegazza, Antonio Gambardella
Vydáno 2013Revisão -
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Modulatory Proteins Can Rescue a Trafficking Defective Epileptogenic Na<sub>v</sub>1.1 Na<sup>+</sup>Channel Mutant Autor Raffaella Rusconi, Paolo Scalmani, Rita Restano‐Cassulini, Giulia Giunti, Antonio Gambardella, Silvana Franceschetti, Grazia Annesi, Enzo Wanke, Massimo Mantegazza
Vydáno 2007Artigo -
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The L444P Gba1 mutation enhances alpha-synuclein induced loss of nigral dopaminergic neurons in mice Autor Anna Migdalska‐Richards, Michał Węgrzynowicz, Raffaella Rusconi, Giulio Deangeli, Donato A. Di Monte, Maria Grazia Spillantini, Anthony H.V. Schapira
Vydáno 2017Artigo -
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Brain propagation of transduced α-synuclein involves non-fibrillar protein species and is enhanced in α-synuclein null mice Autor Michael Helwig, Michael Klinkenberg, Raffaella Rusconi, Ruth E. Musgrove, Nour K. Majbour, Omar M. A. El‐Agnaf, Ayşe Ulusoy, Donato A. Di Monte
Vydáno 2015Artigo -
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A BAC transgenic mouse model reveals neuron subtype-specific effects of a Generalized Epilepsy with Febrile Seizures Plus (GEFS+) mutation Autor Bin Tang, Karoni Dutt, Ligia A. Papale, Raffaella Rusconi, Anupama Shankar, Jessica Ezzell Hunter, Sérgio Tufik, Frank H. Yu, William A. Catterall, Massimo Mantegazza, Alan L. Goldin, Andrew Escayg
Vydáno 2009Artigo -
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Identification of an Na <sub>v</sub> 1.1 sodium channel (SCN1A) loss-of-function mutation associated with familial simple febrile seizures Autor Massimo Mantegazza, Antonio Gambardella, Raffaella Rusconi, Emanuele Schiavon, Ferdinanda Annesi, Rita Restano‐Cassulini, Angelo Labate, Sara Carrideo, R. Chifari, Maria Paola Canevini, R. Canger, Silvana Franceschetti, Grazia Annesi, Enzo Wanke, Aldo Quattrone
Vydáno 2005Artigo -
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Dravet syndrome patient‐derived neurons suggest a novel epilepsy mechanism Autor Yu Liu, Luis F. Lopez‐Santiago, Yukun Yuan, Julie Miller Jones, Baiyu Zhang, Heather A. O’Malley, Gustavo A. Patiño, Janelle E. O’Brien, Raffaella Rusconi, Ajay Gupta, Robert C. Thompson, Marvin R. Natowicz, Miriam H. Meisler, Lori L. Isom, Jack M. Parent
Vydáno 2013Artigo -
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Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study Autor Patrick May, Simon Girard, Merle Harrer, Dheeraj Reddy Bobbili, Julian Schubert, Stefan Wolking, Felicitas Becker, Pamela Lachance‐Touchette, Caroline Meloche, Micheline Gravel, Cristina Elena Niturad, Julia Knaus, Carolien G. F. de Kovel, Mohamad Toliat, Anne Polvi, Michele Iacomino, Rosa Guerrero, Stéphanie Baulac, Carla Marini, Holger Thiele, Janine Altmüller, Kamel Jabbari, Ann‐Kathrin Ruppert, Wiktor Jurkowski, Dennis Lal, Raffaella Rusconi, Sandrine Cestèle, Benedetta Terragni, Ian D. Coombs, Christopher A. Reid, Pasquale Striano, Hande Çağlayan, Auli Sirén, Kate V. Everett, Rikke S. Møller, Helle Hjalgrim, Hiltrud Muhle, Ingo Helbig, Wolfram S. Kunz, Yvonne G. Weber, Sarah Weckhuysen, Peter De Jonghe, Sanjay M. Sisodiya, Rima Nabbout, Silvana Franceschetti, Antonietta Coppola, Maria Stella Vari, Dorothee Kasteleijn‐Nolst Trenité, Betül Baykan, Uğur Özbek, Nerses Bebek, Karl Martin Klein, Felix Rosenow, Dang Khoa Nguyen, François Dubeau, Lionel Carmant, Anne Lortie, Richard Desbiens, Jean-François Clément, Cécile Cieuta‐Walti, Graeme J. Sills, Pauls Auce, Ben Francis, Michael R. Johnson, Anthony G Marson, Bianca Berghuis, Josemir W. Sander, Andreja Avberšek, Mark McCormack, Gianpiero L. Cavalleri, Norman Delanty, Chantal Depondt, Martin Krenn, Fritz Zimprich, Sarah Peter, Marina Nikanorova, Robert Kraaij, Jeroen van Rooij, Rudi Balling, M. Arfan Ikram, André G. Uitterlinden, G. Avanzini, Stéphanie Schorge, Steven Petrou, Massimo Mantegazza, Thomas Sander, Eric LeGuern, José M. Serratosa, Bobby P.C. Koeleman, Aarno Palotie, Anna‐Elina Lehesjoki, Michael Nothnagel, Peter Nürnberg, Snezana Maljevic, Federico Zara, Patrick Cossette, Roland Krause, Holger Lerche, Patrick May, Simon Girard
Vydáno 2018Artigo
Vyhledávací nástroje:
Související témata
Biology
Neuroscience
Gene
Genetics
Mutation
Chemistry
Epilepsy
Medicine
Organic chemistry
Sodium
Sodium channel
Mutant
Alpha-synuclein
Cell biology
Central nervous system
Disease
Forebrain
Internal medicine
Parkinson's disease
Phenotype
Aura
Dravet syndrome
Familial hemiplegic migraine
Loss function
Migraine
Migraine with aura
Pathology
Pons
Protein subunit
Receptor