Massimo Mantegazza - Publications

CNRS & University of Nice (France) 
Sodium Channels, Neuronal Excitability, Epilepsy, Migraine

47 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2016 De Stasi AM, Farisello P, Marcon I, Cavallari S, Forli A, Vecchia D, Losi G, Mantegazza M, Panzeri S, Carmignoto G, Bacci A, Fellin T. Unaltered Network Activity and Interneuronal Firing During Spontaneous Cortical Dynamics In Vivo in a Mouse Model of Severe Myoclonic Epilepsy of Infancy. Cerebral Cortex (New York, N.Y. : 1991). PMID 26819275 DOI: 10.1093/Cercor/Bhw002  1
2015 Bechi G, Rusconi R, Cestèle S, Striano P, Franceschetti S, Mantegazza M. Rescuable folding defective NaV1.1 (SCN1A) mutants in epilepsy: properties, occurrence, and novel rescuing strategy with peptides targeted to the endoplasmic reticulum. Neurobiology of Disease. 75: 100-14. PMID 25576396 DOI: 10.1016/J.Nbd.2014.12.028  1
2015 Mantegazza M, Rusconi R, Cestèle S. Mutations of ion channels in genetic epilepsies Epilepsy Towards the Next Decade: New Trends and Hopes in Epileptology. 15-34. DOI: 10.1007/978-3-319-12283-0_2  1
2014 Hedrich UB, Liautard C, Kirschenbaum D, Pofahl M, Lavigne J, Liu Y, Theiss S, Slotta J, Escayg A, Dihné M, Beck H, Mantegazza M, Lerche H. Impaired action potential initiation in GABAergic interneurons causes hyperexcitable networks in an epileptic mouse model carrying a human Na(V)1.1 mutation. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 34: 14874-89. PMID 25378155 DOI: 10.1523/Jneurosci.0721-14.2014  1
2014 Li T, Tian C, Scalmani P, Frassoni C, Mantegazza M, Wang Y, Yang M, Wu S, Shu Y. Action potential initiation in neocortical inhibitory interneurons. Plos Biology. 12: e1001944. PMID 25203314 DOI: 10.1371/Journal.Pbio.1001944  1
2014 Carlessi L, Fusar Poli E, Bechi G, Mantegazza M, Pascucci B, Narciso L, Dogliotti E, Sala C, Verpelli C, Lecis D, Delia D. Functional and molecular defects of hiPSC-derived neurons from patients with ATM deficiency. Cell Death & Disease. 5: e1342. PMID 25032865 DOI: 10.1038/Cddis.2014.310  1
2014 Guerrini R, Marini C, Mantegazza M. Genetic epilepsy syndromes without structural brain abnormalities: clinical features and experimental models. Neurotherapeutics : the Journal of the American Society For Experimental Neurotherapeutics. 11: 269-85. PMID 24664660 DOI: 10.1007/S13311-014-0267-0  1
2013 Verpelli C, Carlessi L, Bechi G, Fusar Poli E, Orellana D, Heise C, Franceschetti S, Mantegazza R, Mantegazza M, Delia D, Sala C. Comparative neuronal differentiation of self-renewing neural progenitor cell lines obtained from human induced pluripotent stem cells. Frontiers in Cellular Neuroscience. 7: 175. PMID 24109433 DOI: 10.3389/Fncel.2013.00175  1
2013 Cestèle S, Schiavon E, Rusconi R, Franceschetti S, Mantegazza M. Nonfunctional NaV1.1 familial hemiplegic migraine mutant transformed into gain of function by partial rescue of folding defects. Proceedings of the National Academy of Sciences of the United States of America. 110: 17546-51. PMID 24101488 DOI: 10.1073/Pnas.1309827110  1
2013 Partemi S, Cestèle S, Pezzella M, Campuzano O, Paravidino R, Pascali VL, Zara F, Tassinari CA, Striano S, Oliva A, Brugada R, Mantegazza M, Striano P. Loss-of-function KCNH2 mutation in a family with long QT syndrome, epilepsy, and sudden death. Epilepsia. 54: e112-6. PMID 23899126 DOI: 10.1111/Epi.12259  1
2013 Liautard C, Scalmani P, Carriero G, de Curtis M, Franceschetti S, Mantegazza M. Hippocampal hyperexcitability and specific epileptiform activity in a mouse model of Dravet syndrome. Epilepsia. 54: 1251-61. PMID 23663038 DOI: 10.1111/Epi.12213  1
2013 Cestèle S, Labate A, Rusconi R, Tarantino P, Mumoli L, Franceschetti S, Annesi G, Mantegazza M, Gambardella A. Divergent effects of the T1174S SCN1A mutation associated with seizures and hemiplegic migraine. Epilepsia. 54: 927-35. PMID 23398611 DOI: 10.1111/Epi.12123  1
2013 Colombo E, Franceschetti S, Avanzini G, Mantegazza M. Phenytoin inhibits the persistent sodium current in neocortical neurons by modifying its inactivation properties. Plos One. 8: e55329. PMID 23383157 DOI: 10.1371/Journal.Pone.0055329  1
2012 Goaillard JM, Groc L, Lévi S, Mantegazza M, Matifat F, Morel JL, Baron-Forster A. The 22nd ion channel meeting, september 2011, france. Channels (Austin, Tex.). 6: 149-53. PMID 22647366 DOI: 10.4161/Chan.20795  1
2012 Bechi G, Scalmani P, Schiavon E, Rusconi R, Franceschetti S, Mantegazza M. Pure haploinsufficiency for Dravet syndrome Na(V)1.1 (SCN1A) sodium channel truncating mutations. Epilepsia. 53: 87-100. PMID 22150645 DOI: 10.1111/J.1528-1167.2011.03346.X  1
2011 Mantegazza M. Dravet syndrome: insights from in vitro experimental models. Epilepsia. 52: 62-9. PMID 21463283 DOI: 10.1111/J.1528-1167.2011.03005.X  1
2010 Marini C, Mantegazza M. Na+ channelopathies and epilepsy: recent advances and new perspectives. Expert Review of Clinical Pharmacology. 3: 371-84. PMID 22111617 DOI: 10.1586/Ecp.10.20  1
2010 Mantegazza M, Rusconi R, Scalmani P, Avanzini G, Franceschetti S. Epileptogenic ion channel mutations: from bedside to bench and, hopefully, back again. Epilepsy Research. 92: 1-29. PMID 20828990 DOI: 10.1016/J.Eplepsyres.2010.08.003  1
2010 Mantegazza M, Curia G, Biagini G, Ragsdale DS, Avoli M. Voltage-gated sodium channels as therapeutic targets in epilepsy and other neurological disorders. The Lancet. Neurology. 9: 413-24. PMID 20298965 DOI: 10.1016/S1474-4422(10)70059-4  1
2010 Mantegazza M, Catterall WA. Voltage-gated Na+ channels and epilepsy Epilepsia. 51: 9. DOI: 10.1111/J.1528-1167.2010.02795.X  1
2009 Riva D, Vago C, Pantaleoni C, Bulgheroni S, Mantegazza M, Franceschetti S. Progressive neurocognitive decline in two children with Dravet syndrome, de novo SCN1A truncations and different epileptic phenotypes. American Journal of Medical Genetics. Part A. 149: 2339-45. PMID 19764027 DOI: 10.1002/Ajmg.A.33029  1
2009 Tang B, Dutt K, Papale L, Rusconi R, Shankar A, Hunter J, Tufik S, Yu FH, Catterall WA, Mantegazza M, Goldin AL, Escayg A. A BAC transgenic mouse model reveals neuron subtype-specific effects of a Generalized Epilepsy with Febrile Seizures Plus (GEFS+) mutation. Neurobiology of Disease. 35: 91-102. PMID 19409490 DOI: 10.1016/J.Nbd.2009.04.007  1
2009 Rusconi R, Combi R, Cestèle S, Grioni D, Franceschetti S, Dalprà L, Mantegazza M. A rescuable folding defective Nav1.1 (SCN1A) sodium channel mutant causes GEFS+: common mechanism in Nav1.1 related epilepsies? Human Mutation. 30: E747-60. PMID 19402159 DOI: 10.1002/Humu.21041  1
2008 Cestèle S, Scalmani P, Rusconi R, Terragni B, Franceschetti S, Mantegazza M. Self-limited hyperexcitability: functional effect of a familial hemiplegic migraine mutation of the Nav1.1 (SCN1A) Na+ channel. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 28: 7273-83. PMID 18632931 DOI: 10.1523/Jneurosci.4453-07.2008  1
2007 Rusconi R, Scalmani P, Cassulini RR, Giunti G, Gambardella A, Franceschetti S, Annesi G, Wanke E, Mantegazza M. Modulatory proteins can rescue a trafficking defective epileptogenic Nav1.1 Na+ channel mutant. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 27: 11037-46. PMID 17928445 DOI: 10.1523/Jneurosci.3515-07.2007  1
2007 Avanzini G, Franceschetti S, Mantegazza M. Epileptogenic channelopathies: experimental models of human pathologies. Epilepsia. 48: 51-64. PMID 17571353 DOI: 10.1111/J.1528-1167.2007.01067.X  1
2007 Colosimo E, Gambardella A, Mantegazza M, Labate A, Rusconi R, Schiavon E, Annesi F, Cassulini RR, Carrideo S, Chifari R, Canevini MP, Canger R, Franceschetti S, Annesi G, Wanke E, et al. Electroclinical features of a family with simple febrile seizures and temporal lobe epilepsy associated with SCN1A loss-of-function mutation. Epilepsia. 48: 1691-6. PMID 17565594 DOI: 10.1111/J.1528-1167.2007.01153.X  1
2007 Curia G, Aracri P, Colombo E, Scalmani P, Mantegazza M, Avanzini G, Franceschetti S. Phosphorylation of sodium channels mediated by protein kinase-C modulates inhibition by topiramate of tetrodotoxin-sensitive transient sodium current. British Journal of Pharmacology. 150: 792-7. PMID 17279091 DOI: 10.1038/Sj.Bjp.0707144  1
2006 Scalmani P, Rusconi R, Armatura E, Zara F, Avanzini G, Franceschetti S, Mantegazza M. Effects in neocortical neurons of mutations of the Na(v)1.2 Na+ channel causing benign familial neonatal-infantile seizures. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 10100-9. PMID 17021166 DOI: 10.1523/Jneurosci.2476-06.2006  1
2006 Yu FH, Mantegazza M, Westenbroek RE, Robbins CA, Kalume F, Burton KA, Spain WJ, McKnight GS, Scheuer T, Catterall WA. Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy. Nature Neuroscience. 9: 1142-9. PMID 16921370 DOI: 10.1038/Nn1754  1
2006 Aracri P, Colombo E, Mantegazza M, Scalmani P, Curia G, Avanzini G, Franceschetti S. Layer-specific properties of the persistent sodium current in sensorimotor cortex. Journal of Neurophysiology. 95: 3460-8. PMID 16467432 DOI: 10.1152/Jn.00588.2005  1
2006 Colosimo E, Gambardella A, Mantegazza M, Labate A, Rusconi R, Schiavon E, Annesi F, Cassulini RR, Carrideo S, Chifari R, Canevini MP, Canger R, Franceschetti S, Annesi G, Wanke E, et al. Electroclinical features of a family with SCN1A loss-of-function mutation associated with simple febrile seizures | Caratteristiche elettrocliniche di una famiglia con convulsioni febbrili semplici associata a mutazione con perdita della funzione di SCN1A Bollettino - Lega Italiana Contro L'Epilessia. 265-266.  1
2005 Mantegazza M, Gambardella A, Rusconi R, Schiavon E, Annesi F, Cassulini RR, Labate A, Carrideo S, Chifari R, Canevini MP, Canger R, Franceschetti S, Annesi G, Wanke E, Quattrone A. Identification of an Nav1.1 sodium channel (SCN1A) loss-of-function mutation associated with familial simple febrile seizures. Proceedings of the National Academy of Sciences of the United States of America. 102: 18177-82. PMID 16326807 DOI: 10.1073/Pnas.0506818102  1
2005 Mantegazza M, Cestèle S. Beta-scorpion toxin effects suggest electrostatic interactions in domain II of voltage-dependent sodium channels. The Journal of Physiology. 568: 13-30. PMID 16020455 DOI: 10.1113/Jphysiol.2005.093484  1
2005 Mantegazza M, Yu FH, Powell AJ, Clare JJ, Catterall WA, Scheuer T. Molecular determinants for modulation of persistent sodium current by G-protein betagamma subunits. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 25: 3341-9. PMID 15800189 DOI: 10.1523/Jneurosci.0104-05.2005  1
2005 Srairi-Abid N, Guijarro JI, Benkhalifa R, Mantegazza M, Cheikh A, Ben Aissa M, Haumont PY, Delepierre M, El Ayeb M. A new type of scorpion Na+-channel-toxin-like polypeptide active on K+ channels. The Biochemical Journal. 388: 455-64. PMID 15656785 DOI: 10.1042/Bj20041407  1
2004 M'Barek S, Fajloun Z, Cestèle S, Devaux C, Mansuelle P, Mosbah A, Jouirou B, Mantegazza M, Van Rietschoten J, El Ayeb M, Rochat H, Sabatier JM, Sampieri F. First chemical synthesis of a scorpion alpha-toxin affecting sodium channels: the Aah I toxin of Androctonus australis hector. Journal of Peptide Science : An Official Publication of the European Peptide Society. 10: 666-77. PMID 15568681 DOI: 10.1002/Psc.582  1
2004 Curia G, Aracri P, Sancini G, Mantegazza M, Avanzini G, Franceschetti S. Protein-kinase C-dependent phosphorylation inhibits the effect of the antiepileptic drug topiramate on the persistent fraction of sodium currents. Neuroscience. 127: 63-8. PMID 15219669 DOI: 10.1016/J.Neuroscience.2004.04.040  1
2001 Mantegazza M, Yu FH, Catterall WA, Scheuer T. Role of the C-terminal domain in inactivation of brain and cardiac sodium channels. Proceedings of the National Academy of Sciences of the United States of America. 98: 15348-53. PMID 11742069 DOI: 10.1073/Pnas.211563298  1
2001 Cestèle S, Scheuer T, Mantegazza M, Rochat H, Catterall WA. Neutralization of gating charges in domain II of the sodium channel alpha subunit enhances voltage-sensor trapping by a beta-scorpion toxin. The Journal of General Physiology. 118: 291-302. PMID 11524459 DOI: 10.1085/Jgp.118.3.291  1
1999 Taverna S, Sancini G, Mantegazza M, Franceschetti S, Avanzini G. Inhibition of transient and persistent Na+ current fractions by the new anticonvulsant topiramate. The Journal of Pharmacology and Experimental Therapeutics. 288: 960-8. PMID 10027832  1
1998 Taverna S, Mantegazza M, Franceschetti S, Avanzini G. Valproate selectively reduces the persistent fraction of Na+ current in neocortical neurons. Epilepsy Research. 32: 304-8. PMID 9761329 DOI: 10.1016/S0920-1211(98)00060-6  1
1998 Magistretti J, Mantegazza M, de Curtis M, Wanke E. Modalities of distortion of physiological voltage signals by patch-clamp amplifiers: a modeling study. Biophysical Journal. 74: 831-42. PMID 9533695 DOI: 10.1016/S0006-3495(98)74007-X  1
1998 Mantegazza M, Franceschetti S, Avanzini G. Anemone toxin (ATX II)-induced increase in persistent sodium current: effects on the firing properties of rat neocortical pyramidal neurones. The Journal of Physiology. 507: 105-16. PMID 9490824 DOI: 10.1111/J.1469-7793.1998.105Bu.X  1
1996 Magistretti J, Mantegazza M, Guatteo E, Wanke E. Action potentials recorded with patch-clamp amplifiers: are they genuine? Trends in Neurosciences. 19: 530-4. PMID 8961481 DOI: 10.1016/S0166-2236(96)40004-2  1
1995 Mantegazza M, Fasolato C, Hescheler J, Pietrobon D. Stimulation of single L-type calcium channels in rat pituitary GH3 cells by thyrotropin-releasing hormone. The Embo Journal. 14: 1075-83. PMID 7720698  1
1994 Wanke E, Bianchi L, Mantegazza M, Guatteo E, Mancinelli E, Ferroni A. Muscarinic regulation of Ca2+ currents in rat sensory neurons: channel and receptor types, dose-response relationships and cross-talk pathways. The European Journal of Neuroscience. 6: 381-91. PMID 8019675 DOI: 10.1111/J.1460-9568.1994.Tb00281.X  1
Show low-probability matches.