檢索結果 - Massimo Mantegazza

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  1. 1
    <i><scp>SCN</scp>1A</i>/Na<sub>V</sub>1.1 channelopathies: Mechanisms in expression systems, animal models, and human <scp>iPSC</scp> models

    <i><scp>SCN</scp>1A</i>/Na<sub>V</sub>1.1 channelopathies: Mechanisms in expression systems, animal models, and human <scp>iPSC</scp> models 由 Massimo Mantegazza, Vania Broccoli

    出版 2019
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  2. 2
    Epileptogenic Channelopathies: Experimental Models of Human Pathologies

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

    出版 2007
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  3. 3
    Genetic Epilepsy Syndromes Without Structural Brain Abnormalities: Clinical Features and Experimental Models

    Genetic Epilepsy Syndromes Without Structural Brain Abnormalities: Clinical Features and Experimental Models 由 Renzo Guerrini, Carla Marini, Massimo Mantegazza

    出版 2014
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  4. 4
    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 由 Massimo Mantegazza, Silvana Franceschetti, G. Avanzini

    出版 1998
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  5. 5
    Sodium channelopathies of skeletal muscle and brain

    Sodium channelopathies of skeletal muscle and brain 由 Massimo Mantegazza, Sandrine Cestèle, William A. Catterall

    出版 2021
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  6. 6
    Role of the C-terminal domain in inactivation of brain and cardiac sodium channels

    Role of the C-terminal domain in inactivation of brain and cardiac sodium channels 由 Massimo Mantegazza, Frank H. Yu, William A. Catterall, Todd Scheuer

    出版 2001
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  7. 7
    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 由 Sandrine Cestèle, Emanuele Schiavon, Raffaella Rusconi, Silvana Franceschetti, Massimo Mantegazza

    出版 2013
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  8. 8
    Involvement of GABAergic Interneuron Subtypes in 4-Aminopyridine-Induced Seizure-Like Events in Mouse Entorhinal Cortex<i>in Vitro</i>

    Involvement of GABAergic Interneuron Subtypes in 4-Aminopyridine-Induced Seizure-Like Events in Mouse Entorhinal Cortex<i>in Vitro</i> 由 Paolo Scalmani, Rosina Paterra, Massimo Mantegazza, Massimo Avoli, Marco de Curtis

    出版 2023
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  9. 9
    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 由 Sandrine Cestèle, Paolo Scalmani, Raffaella Rusconi, Benedetta Terragni, Silvana Franceschetti, Massimo Mantegazza

    出版 2008
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  10. 10
    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 由 Giulia Bechi, Paolo Scalmani, Emanuele Schiavon, Raffaella Rusconi, Silvana Franceschetti, Massimo Mantegazza

    出版 2011
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  11. 11
    Developmental and epileptic encephalopathies: from genetic heterogeneity to phenotypic continuum

    Developmental and epileptic encephalopathies: from genetic heterogeneity to phenotypic continuum 由 Renzo Guerrini, Valerio Conti, Massimo Mantegazza, Simona Balestrini, Aristea S. Galanopoulou, Fabio Benfenati

    出版 2022
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  12. 12
    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 由 Camille Liautard, Paolo Scalmani, Giovanni Carriero, Marco de Curtis, Silvana Franceschetti, Massimo Mantegazza

    出版 2013
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  13. 13
    Gain of Function for the SCN1A/hNav1.1-L1670W Mutation Responsible for Familial Hemiplegic Migraine

    Gain of Function for the SCN1A/hNav1.1-L1670W Mutation Responsible for Familial Hemiplegic Migraine 由 Sandra Dhifallah, Eric Lancaster, Shana L. Merrill, Nathalie Leroudier, Massimo Mantegazza, Sandrine Cestèle

    出版 2018
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  14. 14
    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 由 Paolo Scalmani, Raffaella Rusconi, Elena Armatura, Federico Zara, G. Avanzini, Silvana Franceschetti, Massimo Mantegazza

    出版 2006
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  15. 15
    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? 由 Raffaella Rusconi, Romina Combi, Sandrine Cestèle, Daniele Grioni, Silvana Franceschetti, Leda DalprÃ, Massimo Mantegazza

    出版 2009
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  16. 16
    Molecular Determinants for Modulation of Persistent Sodium Current by G-Protein βγ Subunits

    Molecular Determinants for Modulation of Persistent Sodium Current by G-Protein βγ Subunits 由 Massimo Mantegazza, Frank H. Yu, Andrew J. Powell, Jeffrey J. Clare, William A. Catterall, Todd Scheuer

    出版 2005
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  17. 17
    Neurodevelopmental defects in Dravet syndrome Scn1a+/− mice: Targeting GABA-switch rescues behavioral dysfunctions but not seizures and mortality

    Neurodevelopmental defects in Dravet syndrome Scn1a+/− mice: Targeting GABA-switch rescues behavioral dysfunctions but not seizures and mortality 由 Lara Pizzamiglio, Fabrizio Capitano, Evgeniia Rusina, G Fossati, Elisabetta Menna, Isabelle Léna, Flavia Antonucci, Massimo Mantegazza

    出版 2025
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  18. 18
    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 由 Sandrine Cestèle, Angelo Labate, Raffaella Rusconi, Patrizia Tarantino, Laura Mumoli, Silvana Franceschetti, Grazia Annesi, Massimo Mantegazza, Antonio Gambardella

    出版 2013
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  19. 19
    Action Potential Initiation in Neocortical Inhibitory Interneurons

    Action Potential Initiation in Neocortical Inhibitory Interneurons 由 Tun Li, Cuiping Tian, Paolo Scalmani, Carolina Frassoni, Massimo Mantegazza, Yonghong Wang, Mingpo Yang, Si Wu, Yousheng Shu

    出版 2014
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  20. 20
    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 由 Raffaella Rusconi, Paolo Scalmani, Rita Restano‐Cassulini, Giulia Giunti, Antonio Gambardella, Silvana Franceschetti, Grazia Annesi, Enzo Wanke, Massimo Mantegazza

    出版 2007
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