Výsledky vyhledávání - Silvana Franceschetti

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  1. 1
    Epileptogenic Channelopathies: Experimental Models of Human Pathologies

    Epileptogenic Channelopathies: Experimental Models of Human Pathologies Autor G. Avanzini, Silvana Franceschetti, Massimo Mantegazza

    Vydáno 2007
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  2. 2
    Anemone toxin (ATX II)‐induced increase in persistent sodium current: effects on the firing properties of rat neocortical pyramidal neurones

    Anemone toxin (ATX II)‐induced increase in persistent sodium current: effects on the firing properties of rat neocortical pyramidal neurones Autor Massimo Mantegazza, Silvana Franceschetti, G. Avanzini

    Vydáno 1998
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  3. 3
    Nonfunctional Na <sub>V</sub> 1.1 familial hemiplegic migraine mutant transformed into gain of function by partial rescue of folding defects

    Nonfunctional Na <sub>V</sub> 1.1 familial hemiplegic migraine mutant transformed into gain of function by partial rescue of folding defects Autor Sandrine Cestèle, Emanuele Schiavon, Raffaella Rusconi, Silvana Franceschetti, Massimo Mantegazza

    Vydáno 2013
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  4. 4
    Identification of the Epileptogenic Zone from Stereo-EEG Signals: A Connectivity-Graph Theory Approach

    Identification of the Epileptogenic Zone from Stereo-EEG Signals: A Connectivity-Graph Theory Approach Autor Ferruccio Panzica, Giulia Varotto, Fabio Rotondi, Roberto Spreafico, Silvana Franceschetti

    Vydáno 2013
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  5. 5
    Theory of mind and epilepsy: What clinical implications?

    Theory of mind and epilepsy: What clinical implications? Autor Anna Rıta Gıovagnolı, Annalisa Parente, Flavio Villani, Silvana Franceschetti, Roberto Spreafico

    Vydáno 2013
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  6. 6
    Self-Limited Hyperexcitability: Functional Effect of a Familial Hemiplegic Migraine Mutation of the Na<sub>v</sub>1.1 (SCN1A) Na<sup>+</sup>Channel

    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 2008
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  7. 7
    Pure haploinsufficiency for Dravet syndrome Na<sub>V</sub>1.1 (<i>SCN1A</i>) sodium channel truncating mutations

    Pure haploinsufficiency for Dravet syndrome Na<sub>V</sub>1.1 (<i>SCN1A</i>) sodium channel truncating mutations Autor Giulia Bechi, Paolo Scalmani, Emanuele Schiavon, Raffaella Rusconi, Silvana Franceschetti, Massimo Mantegazza

    Vydáno 2011
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  8. 8
    Hippocampal hyperexcitability and specific epileptiform activity in a mouse model of <scp>D</scp>ravet syndrome

    Hippocampal hyperexcitability and specific epileptiform activity in a mouse model of <scp>D</scp>ravet syndrome Autor Camille Liautard, Paolo Scalmani, Giovanni Carriero, Marco de Curtis, Silvana Franceschetti, Massimo Mantegazza

    Vydáno 2013
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  9. 9
    Effects in Neocortical Neurons of Mutations of the Na<sub>v</sub>1.2 Na<sup>+</sup>Channel causing Benign Familial Neonatal-Infantile Seizures

    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 2006
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  10. 10
    Transcutaneous vagal nerve stimulatio (t-VNS): An adjunctive treatment option for refractory epilepsy

    Transcutaneous vagal nerve stimulatio (t-VNS): An adjunctive treatment option for refractory epilepsy Autor Giuseppina Barbella, Isabella Cocco, Elena Freri, Guia Marotta, Elisa Visani, Silvana Franceschetti, Marina Casazza

    Vydáno 2018
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  11. 11
    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?

    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 2009
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  12. 12
    Divergent effects of the <scp>T</scp>1174S <scp><i>SCN1A</i></scp> mutation associated with seizures and hemiplegic migraine

    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 2013
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  13. 13
    Modulatory Proteins Can Rescue a Trafficking Defective Epileptogenic Na<sub>v</sub>1.1 Na<sup>+</sup>Channel Mutant

    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 2007
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  14. 14
    Recurrent generalized seizures, visual loss, and palinopsia as phenotypic features of neuronal ceroid lipofuscinosis due to progranulin gene mutation

    Recurrent generalized seizures, visual loss, and palinopsia as phenotypic features of neuronal ceroid lipofuscinosis due to progranulin gene mutation Autor Laura Canafoglia, Michela Morbin, V. Scaioli, Davide Pareyson, Ludovico D’Incerti, Valeria Fugnanesi, Fabrizio Tagliavini, Samuel F. Berkovic, Silvana Franceschetti

    Vydáno 2014
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  15. 15
    Activity-dependent phosphorylation of Ser187 is required for SNAP-25-negative modulation of neuronal voltage-gated calcium channels

    Activity-dependent phosphorylation of Ser187 is required for SNAP-25-negative modulation of neuronal voltage-gated calcium channels Autor Davide Pozzi, Steven B. Condliffe, Yuri Bozzi, Maia Chikhladze, Carlotta Grumelli, Véronique Proux‐Gillardeaux, Masami Takahashi, Silvana Franceschetti, Claudia Verderio, Michela Matteoli

    Vydáno 2007
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  16. 16
    Clinical and neurophysiologic features of progressive myoclonus epilepsy without renal failure caused by<i>SCARB2</i>mutations

    Clinical and neurophysiologic features of progressive myoclonus epilepsy without renal failure caused by<i>SCARB2</i>mutations Autor 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

    Vydáno 2011
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  17. 17
    Recessive Loss-of-Function Mutation in the Pacemaker HCN2 Channel Causing Increased Neuronal Excitability in a Patient with Idiopathic Generalized Epilepsy

    Recessive Loss-of-Function Mutation in the Pacemaker HCN2 Channel Causing Increased Neuronal Excitability in a Patient with Idiopathic Generalized Epilepsy Autor Jacopo C. DiFrancesco, Andrea Barbuti, Raffaella Milanesi, Stefania Coco, Annalisa Bucchi, Georgia Bottelli, Carlo Ferrarese, Silvana Franceschetti, Benedetta Terragni, Mirko Baruscotti, Dario DiFrancesco

    Vydáno 2011
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  18. 18
    Focal epilepsies in adult patients attending two epilepsy centers: Classification of drug‐resistance, assessment of risk factors, and usefulness of “new” antiepileptic drugs

    Focal epilepsies in adult patients attending two epilepsy centers: Classification of drug‐resistance, assessment of risk factors, and usefulness of “new” antiepileptic drugs Autor 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

    Vydáno 2012
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  19. 19
    Electroclinical spectrum of the neuronal ceroid lipofuscinoses associated with <i>CLN6</i> mutations

    Electroclinical spectrum of the neuronal ceroid lipofuscinoses associated with <i>CLN6</i> mutations Autor 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

    Vydáno 2015
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  20. 20
    hERG1 channels are overexpressed in glioblastoma multiforme and modulate VEGF secretion in glioblastoma cell lines

    hERG1 channels are overexpressed in glioblastoma multiforme and modulate VEGF secretion in glioblastoma cell lines Autor 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

    Vydáno 2005
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