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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

Publication date

January 2006

DOI

10.1038/sj.ejhg.5201607

Publisher

Springer Science and Business Media LLC

Abstract

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

Extracted data

Related items

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

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CACNA1A R1347Q: a frequent recurrent mutation in hemiplegic migraine.

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Terwindt, G.M.

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

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

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.
BROOS, L. A.
KIA, S. K.
VAN DEN HEUVEL, J. J.
BLACK, D. F.
HAAN, J.
FRANTS, R. R.
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CASARI, G.
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Familial hemiplegic migraine (FHM) is a rare autosomal dominantly inherited subtype of migraine, in ...

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

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

Todt, U.
Dichgans, M.
Jurkat-Rott, K.
Heinze, A.
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Koenderink, J.B.
Goebel, I.
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Friedrich, T.
Gobel, H.
Kubisch, C.

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

Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraine.

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Lemos, C.
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Amino acid changes in the amino terminus of the Na,K-adenosine triphosphatase alpha-2 subunit associated to familial and sporadic hemiplegic migraine

A. Tonelli
A. Gallanti
A. Bersano
V. Cardin
G. Airoldi
F. Redaelli
MT Bassi
E Ballabio
L Candelise
N Bresolin

January 2007

Familial hemiplegic migraine (FHM) is a rare subtype of migraine with aura inherited with an autosom...

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

E. Martínez
R. Moreno
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I. Vidriales
M. Ruiz
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January 2016

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

A novel de novo nonsense mutation in ATP1A2 associated with sporadic hemiplegic migraine and epileptic seizures

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V. Cardin
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January 2008

Familial hemiplegic migraine (FHM) is a severe dominant form of migraine with aura associated with t...

Na,K-ATPase mutations in familial hemiplegic migraine lead to functional inactivation.

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Qiu, L.Y.
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Friedrich, T.

January 2005

Contains fulltext : 48917.pdf (publisher's version ) (Closed access)The Na,K-ATPas...

Familial hemiplegic migraine mutations affect Na,K-ATPase domain interactions

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AbstractFamilial hemiplegic migraine (FHM) is a monogenic variant of migraine with aura. One of the ...

ATP1A2 mutations in 11 families with familial hemiplegic migraine.

Riant, F.
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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

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...

Familial hemiplegic migraine mutations affect Na,K-ATPase domain interactions

Swarts, H.G.P.
Weigand, K.M.
Venselaar, H.
Maagdenberg, A.M. van den
Russel, F.G.M.
Koenderink, J.B.

January 2013

Familial hemiplegic migraine (FHM) is a monogenic variant of migraine with aura. One of the three kn...

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...

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...

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.
BROOS, L. A.
KIA, S. K.
VAN DEN HEUVEL, J. J.
BLACK, D. F.
HAAN, J.
FRANTS, R. R.
BARONE, V.
FERRARI, M. D.
CASARI, G.
KOENDERINK, J. B.
VAN DEN MAAGDENBERG, A. M.

January 2006

Familial hemiplegic migraine (FHM) is a rare autosomal dominantly inherited subtype of migraine, in ...

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...

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 ...

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...

Alterations in the {alpha}2 isoform of Na,K-ATPase associated with familial hemiplegic migraine type 2

Segall, Laura
Mezzetti, Alessandra
Scanzano, Rosemarie
Gargus, J. Jay
Purisima, Enrico
Blostein, Rhoda

January 2005

A number of missense mutations in the Na,K-ATPase alpha2 catalytic subunit have been identified in f...

Amino acid changes in the amino terminus of the Na,K-adenosine triphosphatase alpha-2 subunit associated to familial and sporadic hemiplegic migraine

A. Tonelli
A. Gallanti
A. Bersano
V. Cardin
G. Airoldi
F. Redaelli
MT Bassi
E Ballabio
L Candelise
N Bresolin

January 2007

Familial hemiplegic migraine (FHM) is a rare subtype of migraine with aura inherited with an autosom...

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...

A novel de novo nonsense mutation in ATP1A2 associated with sporadic hemiplegic migraine and epileptic seizures

A. Gallanti
A. Tonelli
V. Cardin
G. Bussone
M. Bassi
N. Bresolin

January 2008

Familial hemiplegic migraine (FHM) is a severe dominant form of migraine with aura associated with t...

Na,K-ATPase mutations in familial hemiplegic migraine lead to functional inactivation.

Koenderink, J.B.
Zifarelli, G.
Qiu, L.Y.
Schwarz, W.
Pont, J.J.H.H.M. de
Bamberg, E.
Friedrich, T.

January 2005

Contains fulltext : 48917.pdf (publisher's version ) (Closed access)The Na,K-ATPas...

Familial hemiplegic migraine mutations affect Na,K-ATPase domain interactions

Swarts, Herman G.P.
Weigand, Karl M.
Venselaar, Hanka
van den Maagdenberg, Arn M. J.M.
Russel, Frans G.M.
Koenderink, Jan B.

December 2013

AbstractFamilial hemiplegic migraine (FHM) is a monogenic variant of migraine with aura. One of the ...

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

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...

Familial hemiplegic migraine mutations affect Na,K-ATPase domain interactions

Swarts, H.G.P.
Weigand, K.M.
Venselaar, H.
Maagdenberg, A.M. van den
Russel, F.G.M.
Koenderink, J.B.

January 2013

Familial hemiplegic migraine (FHM) is a monogenic variant of migraine with aura. One of the three kn...

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...