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To cite this version:

Paolo Scalmani
Raffaella Rusconi
Benedetta Terragni
Silvana Franceschetti
Massimo Mantegazza
Paolo Scalmani
Raffaella Rusconi
Benedetta Terragni
Silvana Franceschetti
Hal Id Inserm
Cest Leè S
Scalmani Paolo
Rusconi Raffaella
Terragni Benedetta
Franceschetti Silvana
Mantegazza Massimo

Publication date

January 2009

Abstract

hyperexcitability: functional effect of a familial hemiplegic migraine mutation of the Nav1.

Extracted data

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Dib-Hajj, S.D.

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Horisberger, J.D.

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Mantegazza, Massimo

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Dhifallah, Sandra
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July 2018

International audienceThe SCN1A gene encodes for the voltage-dependent Nav1.1 Na+ channel, an isofor...

Two de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraine.

Vanmolkot, K.R.
Kors, E.E.
Turk, U.
Turkdogan, D.
Keyser, A.J.M.
Broos, L.A.
Kia, S.K.
Heuvel, J.J.M.W. van den
Black, D.F.
Haan, J.H.A. de

January 2006

Contains fulltext : 51118.pdf (publisher's version ) (Closed access

Two novel functional mutations in the Na+,K+-ATPase alpha2-subunit ATP1A2 gene in patients with familial hemiplegic migraine and associated neurological phenotypes.

Castro, M.J.
Figueiredo Nunes, P.M.
Vries, B. de
Lemos, C.
Vanmolkot, K.R.
Heuvel, J.J.M.W. van den
Temudo, T.
Barros, J.
Sequeiros, J.
Frants, R.R.
Koenderink, J.B.
Pereira-Monteiro, J.M.
Maagdenberg, A.M.J.M. van den

January 2008

Contains fulltext : 70562.pdf (publisher's version ) (Closed access)Mutations in t...

Compound heterozygosity in sodium channel Nav1.7 in a family with hereditary erythermalgia.

Samuels, M.E.
Morsche, R.H.M. te
Lynch, M.E.
Drenth, J.P.H.

January 2008

Contains fulltext : 71477.pdf (publisher's version ) (Open Access)Hereditary eryth...

Habituation of evoked responses is greater in patients with familial hemiplegic migraine than in controls: a contrast with the common forms of migraine.

Hansen, Jacob Moller
Bolla, Monica
Magis, Delphine
De Pasqua, Victor
Ashina, Messoud
Thomsen, L. L.
Olesen, Jens
Schoenen, Jean

January 2011

Background: Familial hemiplegic migraine (FHM) is a rare, dominantly inherited subtype of migraine w...

Intra- and interfamily phenotypic diversity in pain syndromes associated with a gain-of-function variant of NaV1.7.

Estacion, M.
Han, C.
Choi, J.S.
Hoeijmakers, J.G.J.
Lauria, G.
Drenth, J.P.H.
Gerrits, M.M.
Dib-Hajj, S.D.
Faber, C.G.
Merkies, I.S.
Waxman, S.G.

January 2011

Contains fulltext : 96030.pdf (publisher's version ) (Open Access

Diverse functional consequences of mutations in the Na+/K+-ATPase alpha2-subunit causing familial hemiplegic migraine type 2.

Tavraz, N.N.
Friedrich, T.
Durr, K.L.
Koenderink, J.B.
Bamberg, E.
Freilinger, T.
Dichgans, M.

January 2008

Contains fulltext : 70493.pdf (Publisher’s version ) (Open Access)Mutations in ATP...

NaV1.7 gain-of-function mutations as a continuum: A1632E displays physiological changes associated with erythromelalgia and paroxysmal extreme pain disorder mutations and produces symptoms of both disorders.

Estacion, M.
Dib-Hajj, S.D.
Benke, P.J.
Morsche, R.H.M. te
Eastman, E.M.
Macala, L.
Drenth, J.P.H.
Waxman, S.G.

January 2008

Contains fulltext : 70933.pdf (publisher's version ) (Open Access)Gain-of-function...

Divergent effects of the T1174S SCN1A mutation associated with seizures and hemiplegic migraine.

Cestèle, Sandrine
Labate, Angelo
Rusconi, Raffaella
Tarantino, Patrizia
Mumoli, Laura
Franceschetti, Silvana
Annesi, Grazia
Mantegazza, Massimo
Gambardella, Antonio

May 2013

International audiencePURPOSE: To report the identification of the T1174S SCN1A (NaV 1.1) mutation i...

preceding article

Marı́a A G
Ro S
Ricardo Felix

September 2016

The familial hemiplegic migraine type 1 mutation K1336E affects direct G protein-mediated regulation...

CACNA1A R1347Q: a frequent recurrent mutation in hemiplegic migraine.

Stam, A.H.
Vanmolkot, K.R.
Kremer, H.P.H.
Gartner, J.
Brown, J.
Leshinsky-Silver, E.
Gilad, R.
Kors, E.E.
Frankhuizen, W.S.
Ginjaar, H.B.
Haan, J.
Frants, R.R.
Ferrari, M.D.
Maagdenberg, A.M.J.M. van den
Terwindt, G.M.

January 2008

Contains fulltext : 70291.pdf (publisher's version ) (Closed access)Of the 18 miss...

Familial gain-of-function Nav1.9 mutation in a painful channelopathy

Han, C.
Yang, Y
Morsche, R.H. te
Drenth, J.P.H.
Politei, J.M.
Waxman, S.G.
Dib-Hajj, S.D.

January 2017

Item does not contain fulltextOBJECTIVE: Gain-of-function mutations in Nav1.9 have been identified i...

Functional effects of Na+,K+-ATPase gene mutations linked to familial hemiplegic migraine.

Capendeguy, O.
Horisberger, J.D.

January 2004

Familial hemiplegic migraine type 2, an autosomal dominant form of migraine with aura, has been asso...