Որոնման արդյունքները - Silvana Franceschetti
- Ցուցադրվում են 1 - 20 արդյունքները 37
- Գնացեք Հաջորդ էջ
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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 Sandrine Cestèle, Paolo Scalmani, Raffaella Rusconi, Benedetta Terragni, Silvana Franceschetti, Massimo Mantegazza
Հրապարակվել է 2008Artigo -
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Pure haploinsufficiency for Dravet syndrome Na<sub>V</sub>1.1 (<i>SCN1A</i>) sodium channel truncating mutations Giulia Bechi, Paolo Scalmani, Emanuele Schiavon, Raffaella Rusconi, Silvana Franceschetti, Massimo Mantegazza
Հրապարակվել է 2011Artigo -
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Hippocampal hyperexcitability and specific epileptiform activity in a mouse model of <scp>D</scp>ravet syndrome Camille Liautard, Paolo Scalmani, Giovanni Carriero, Marco de Curtis, Silvana Franceschetti, Massimo Mantegazza
Հրապարակվել է 2013Artigo -
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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 Paolo Scalmani, Raffaella Rusconi, Elena Armatura, Federico Zara, G. Avanzini, Silvana Franceschetti, Massimo Mantegazza
Հրապարակվել է 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? Raffaella Rusconi, Romina Combi, Sandrine Cestèle, Daniele Grioni, Silvana Franceschetti, Leda DalprÃ, Massimo Mantegazza
Հրապարակվել է 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 Sandrine Cestèle, Angelo Labate, Raffaella Rusconi, Patrizia Tarantino, Laura Mumoli, Silvana Franceschetti, Grazia Annesi, Massimo Mantegazza, Antonio Gambardella
Հրապարակվել է 2013Revisão -
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Modulatory Proteins Can Rescue a Trafficking Defective Epileptogenic Na<sub>v</sub>1.1 Na<sup>+</sup>Channel Mutant Raffaella Rusconi, Paolo Scalmani, Rita Restano‐Cassulini, Giulia Giunti, Antonio Gambardella, Silvana Franceschetti, Grazia Annesi, Enzo Wanke, Massimo Mantegazza
Հրապարակվել է 2007Artigo -
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Recurrent generalized seizures, visual loss, and palinopsia as phenotypic features of neuronal ceroid lipofuscinosis due to progranulin gene mutation Laura Canafoglia, Michela Morbin, V. Scaioli, Davide Pareyson, Ludovico D’Incerti, Valeria Fugnanesi, Fabrizio Tagliavini, Samuel F. Berkovic, Silvana Franceschetti
Հրապարակվել է 2014Artigo -
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Activity-dependent phosphorylation of Ser187 is required for SNAP-25-negative modulation of neuronal voltage-gated calcium channels Davide Pozzi, Steven B. Condliffe, Yuri Bozzi, Maia Chikhladze, Carlotta Grumelli, Véronique Proux‐Gillardeaux, Masami Takahashi, Silvana Franceschetti, Claudia Verderio, Michela Matteoli
Հրապարակվել է 2007Artigo -
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Clinical and neurophysiologic features of progressive myoclonus epilepsy without renal failure caused by<i>SCARB2</i>mutations Guido Rubboli, Silvana Franceschetti, Samuel F. Berkovic, Laura Canafoglia, Antonio Gambardella, Leanne M. Dibbens, P. Riguzzi, C. Campieri, Adriana Magaudda, C. A. Tassinari, Roberto Michelucci
Հրապարակվել է 2011Artigo -
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Recessive Loss-of-Function Mutation in the Pacemaker HCN2 Channel Causing Increased Neuronal Excitability in a Patient with Idiopathic Generalized Epilepsy Jacopo C. DiFrancesco, Andrea Barbuti, Raffaella Milanesi, Stefania Coco, Annalisa Bucchi, Georgia Bottelli, Carlo Ferrarese, Silvana Franceschetti, Benedetta Terragni, Mirko Baruscotti, Dario DiFrancesco
Հրապարակվել է 2011Artigo -
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Focal epilepsies in adult patients attending two epilepsy centers: Classification of drug‐resistance, assessment of risk factors, and usefulness of “new” antiepileptic drugs Isabella Gilioli, Aglaia Vignoli, Elisa Visani, Marina Casazza, Laura Canafoglia, Valentina Chiesa, Elena Gardella, Francesca La Briola, Ferruccio Panzica, G. Avanzini, Maria Paola Canevini, Silvana Franceschetti, S. Binelli
Հրապարակվել է 2012Artigo -
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Electroclinical spectrum of the neuronal ceroid lipofuscinoses associated with <i>CLN6</i> mutations Laura Canafoglia, Isabella Gilioli, Federica Invernizzi, Vito Sofia, Valeria Fugnanesi, Michela Morbin, Luisa Chiapparini, Tiziana Granata, S. Binelli, V. Scaioli, Barbara Garavaglia, Nardo Nardocci, Samuel F. Berkovic, Silvana Franceschetti
Հրապարակվել է 2015Artigo -
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hERG1 channels are overexpressed in glioblastoma multiforme and modulate VEGF secretion in glioblastoma cell lines Alessio Masi, Andrea Becchetti, Rita Restano‐Cassulini, S. Polvani, Giovanna Hofmann, Anna Maria Buccoliero, Milena Paglierani, Bianca Pollo, Gian Luigi Taddei, Pasquale Gallina, Nicola Di Lorenzo, Silvana Franceschetti, Enzo Wanke, Annarosa Arcangeli
Հրապարակվել է 2005Artigo
Որոնման գործիքներ:
Առնչվող խորագիր
Biology
Genetics
Neuroscience
Gene
Medicine
Epilepsy
Mutation
Internal medicine
Phenotype
Psychology
Chemistry
Disease
Myoclonus
Organic chemistry
Pathology
Mutant
Neuronal ceroid lipofuscinosis
Progressive myoclonus epilepsy
Electroencephalography
Loss function
Psychiatry
Sodium
Age of onset
Cell biology
Receptor
Sodium channel
Audiology
Aura
Biochemistry
Biophysics