Original Article

BRIEF REPORT Psychotic aura symptoms in familial hemiplegic migraine type 2 (ATP1A2)

Jose ́ Barros Alex
Re Mendes Ilda Matos
Jose ́ Pereira-monteiro

August 2016

The Author(s) 2012. This article is published with open access at Springerlink.com Introduction Neur...

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...

Rare missense variants in ATP1A2 in families with clustering of common forms of migraine.

Todt, U.
Dichgans, M.
Jurkat-Rott, K.
Heinze, A.
Zifarelli, G.
Koenderink, J.B.
Goebel, I.
Zumbroich, V.
Stiller, A.
Ramirez, A.
Friedrich, T.
Gobel, H.
Kubisch, C.

January 2005

Contains fulltext : 48486.pdf (publisher's version ) (Closed access)Migraine is a ...

Clinical spectrum in three families with familial hemiplegic migraine type 2 including a novel mutation in the ATP1A2 gene

Roth, Christian
Freilinger, Tobias
Kirovski, Georgi
Dunkel, Juliane
Shah, Yogesh
Wilken, Bernd
Rautenstrauß, Bernd
Ferbert, Andreas

January 2014

Introduction Familial hemiplegic migraine (FHM) is a rare subtype of migraine with transient hemipl...

A novel ATP1A2 mutation in a family with FHM type II

Pierelli, F
Grieco, G
Pauri, F
Pirro, C
Fiermonte, G
Ambrosini, A
Costa, A
Buzzi, M
Valoppi, M
Nappi, G
Santorelli, F.
CALTAGIRONE, CARLO

March 2006

Familial hemiplegic migraine (FHM) is a rare subtype of migraine with aura with an autosomal dominan...

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...

Familial Hemiplegic Migraine with Severe Attacks: A New Report with ATP1A2 Mutation

E. Martínez
R. Moreno
L. López-Mesonero
I. Vidriales
M. Ruiz
A. L. Guerrero
J. J. Tellería

January 2016

Introduction. Familial hemiplegic migraine (FHM) is a rare disorder characterized by migraine attack...

Familial Hemiplegic Migraine With ATP1A2 Mutations

J Gordon Millichap

May 2007

Three children with prolonged hemiplegia following severe unilateral headache and having mutations i...

Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraine.

Castro, M.J.
Stam, A.H.
Lemos, C.
Barros, J.
Gouveia, R.G.
Martins, I.P.
Koenderink, J.B.
Vanmolkot, K.R.
Mendes, A.P.
Frants, R.R.
Ferrari, M.D.
Sequeiros, J.
Pereira-Monteiro, J.M.
Maagdenberg, A.M.J.M. van den

January 2007

Contains fulltext : 53476.pdf (publisher's version ) (Closed access)Familial hemip...

Familial Hemiplegic Migraine: A New Gene in an Italian Family

Pietro Palumbo1#
Orazio Palumbo1#
Francesca Felicia Operto2
Stefano Castellana3
Ester Di Muro1
4
Maria Pia Leone1
Tommaso Biagini3
Grazia Pastorino2
Tommaso Mazza3
Massimo Carella
Giangennaro Coppola

January 2019

Hemiplegic migraine (HM) is a rare form of migraine characterized by severe attacks of unilateral an...

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

Familial hemiplegic migraine type 2 due to a novel missense mutation in ATP1A2

Antonaci, Fabio
Ravaglia, Sabrina
Grieco, Gaetano S
Gagliardi, Stella
Cereda, Cristina
Costa, Alfredo

January 2021

BACKGROUND: The mechanisms of genotype-phenotype interaction in Familiar Hemiplegic migraine type 2 ...

ATP1A2 mutations in 11 families with familial hemiplegic migraine.

Riant, F.
DE FUSCO, M.
Aridon, P.
Ducros, A.
Ploton, C.
Marchelli, F.
Maciazek, J.
Bousser, M.
Casari, G.
TOURNIER LASSERVE, E.

January 2005

Abstract Familial hemiplegic migraine (FHM) is an autosomal dominant form of migraine with aura. Th...

Familial hemiplegic migraine: a new gene in an italian family

Palumbo, Pietro
Palumbo, Orazio
Felicia Operto, Francesca
Castellana, Stefano
DI MURO, ESTER
Leone, Maria Pia
Biagini, Tommaso
Pastorino, Grazia
Mazza, Tommaso
Carella, Massimo
Coppola, Giangennaro

January 2019

Hemiplegic migraine (HM) is a rare form of migraine characterized by severe attacks of unilateral an...

Epilepsy as part of the phenotype associated with ATP1A2 mutations

Deprez, Liesbet
Weckhuysen, Sarah
Peeters, Katelijne
Deconinck, Tine
Claeys, Kristl
Claes, Lieve RF
Suls, Arvid
Van Dyck, Tine
Palmini, André
Matthijs, Gert
Van Paesschen, Wim
De Jonghe, Peter

March 2008

PURPOSE: Mutations in the ATP1A2 gene have been described in families with familial hemiplegic migra...

BRIEF REPORT Psychotic aura symptoms in familial hemiplegic migraine type 2 (ATP1A2)

Jose ́ Barros Alex
Re Mendes Ilda Matos
Jose ́ Pereira-monteiro

August 2016

The Author(s) 2012. This article is published with open access at Springerlink.com Introduction Neur...

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...

Rare missense variants in ATP1A2 in families with clustering of common forms of migraine.

Todt, U.
Dichgans, M.
Jurkat-Rott, K.
Heinze, A.
Zifarelli, G.
Koenderink, J.B.
Goebel, I.
Zumbroich, V.
Stiller, A.
Ramirez, A.
Friedrich, T.
Gobel, H.
Kubisch, C.

January 2005

Contains fulltext : 48486.pdf (publisher's version ) (Closed access)Migraine is a ...

Clinical spectrum in three families with familial hemiplegic migraine type 2 including a novel mutation in the ATP1A2 gene

Roth, Christian
Freilinger, Tobias
Kirovski, Georgi
Dunkel, Juliane
Shah, Yogesh
Wilken, Bernd
Rautenstrauß, Bernd
Ferbert, Andreas

January 2014

Introduction Familial hemiplegic migraine (FHM) is a rare subtype of migraine with transient hemipl...

A novel ATP1A2 mutation in a family with FHM type II

Pierelli, F
Grieco, G
Pauri, F
Pirro, C
Fiermonte, G
Ambrosini, A
Costa, A
Buzzi, M
Valoppi, M
Nappi, G
Santorelli, F.
CALTAGIRONE, CARLO

March 2006

Familial hemiplegic migraine (FHM) is a rare subtype of migraine with aura with an autosomal dominan...

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...

Familial Hemiplegic Migraine with Severe Attacks: A New Report with ATP1A2 Mutation

E. Martínez
R. Moreno
L. López-Mesonero
I. Vidriales
M. Ruiz
A. L. Guerrero
J. J. Tellería

January 2016

Introduction. Familial hemiplegic migraine (FHM) is a rare disorder characterized by migraine attack...

Familial Hemiplegic Migraine With ATP1A2 Mutations

J Gordon Millichap

May 2007

Three children with prolonged hemiplegia following severe unilateral headache and having mutations i...

Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraine.

Castro, M.J.
Stam, A.H.
Lemos, C.
Barros, J.
Gouveia, R.G.
Martins, I.P.
Koenderink, J.B.
Vanmolkot, K.R.
Mendes, A.P.
Frants, R.R.
Ferrari, M.D.
Sequeiros, J.
Pereira-Monteiro, J.M.
Maagdenberg, A.M.J.M. van den

January 2007

Contains fulltext : 53476.pdf (publisher's version ) (Closed access)Familial hemip...

Familial Hemiplegic Migraine: A New Gene in an Italian Family

Pietro Palumbo1#
Orazio Palumbo1#
Francesca Felicia Operto2
Stefano Castellana3
Ester Di Muro1
4
Maria Pia Leone1
Tommaso Biagini3
Grazia Pastorino2
Tommaso Mazza3
Massimo Carella
Giangennaro Coppola

January 2019

Hemiplegic migraine (HM) is a rare form of migraine characterized by severe attacks of unilateral an...

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

Familial hemiplegic migraine type 2 due to a novel missense mutation in ATP1A2

Antonaci, Fabio
Ravaglia, Sabrina
Grieco, Gaetano S
Gagliardi, Stella
Cereda, Cristina
Costa, Alfredo

January 2021

BACKGROUND: The mechanisms of genotype-phenotype interaction in Familiar Hemiplegic migraine type 2 ...

ATP1A2 mutations in 11 families with familial hemiplegic migraine.

Riant, F.
DE FUSCO, M.
Aridon, P.
Ducros, A.
Ploton, C.
Marchelli, F.
Maciazek, J.
Bousser, M.
Casari, G.
TOURNIER LASSERVE, E.

January 2005

Abstract Familial hemiplegic migraine (FHM) is an autosomal dominant form of migraine with aura. Th...

Familial hemiplegic migraine: a new gene in an italian family

Palumbo, Pietro
Palumbo, Orazio
Felicia Operto, Francesca
Castellana, Stefano
DI MURO, ESTER
Leone, Maria Pia
Biagini, Tommaso
Pastorino, Grazia
Mazza, Tommaso
Carella, Massimo
Coppola, Giangennaro

January 2019

Hemiplegic migraine (HM) is a rare form of migraine characterized by severe attacks of unilateral an...

Epilepsy as part of the phenotype associated with ATP1A2 mutations

Deprez, Liesbet
Weckhuysen, Sarah
Peeters, Katelijne
Deconinck, Tine
Claeys, Kristl
Claes, Lieve RF
Suls, Arvid
Van Dyck, Tine
Palmini, André
Matthijs, Gert
Van Paesschen, Wim
De Jonghe, Peter

March 2008

PURPOSE: Mutations in the ATP1A2 gene have been described in families with familial hemiplegic migra...

BRIEF REPORT Psychotic aura symptoms in familial hemiplegic migraine type 2 (ATP1A2)

Jose ́ Barros Alex
Re Mendes Ilda Matos
Jose ́ Pereira-monteiro

August 2016

The Author(s) 2012. This article is published with open access at Springerlink.com Introduction Neur...

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...

Rare missense variants in ATP1A2 in families with clustering of common forms of migraine.

Todt, U.
Dichgans, M.
Jurkat-Rott, K.
Heinze, A.
Zifarelli, G.
Koenderink, J.B.
Goebel, I.
Zumbroich, V.
Stiller, A.
Ramirez, A.
Friedrich, T.
Gobel, H.
Kubisch, C.

January 2005

Contains fulltext : 48486.pdf (publisher's version ) (Closed access)Migraine is a ...

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Original Article

Abstract

Extracted data

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