A new mutation on the ATP1A2 gene in familial basilar migraine

被引:0
|
作者
D'Onofrio, M
Ambrosini, A
Santorelli, FM
Buzzi, MG
Grieco, G
Di Mambro, A
Valoppi, M
Nicoletti, F
Nappi, G
Schoenen, J
Pierelli, F
机构
[1] INM Neuromed, Headache Clin, Pozzilli, Isernia, Italy
[2] Univ Roma La Sapienza, Mondino Tor Vergata S Lucia Ctr Expt Neurobiol, Mol Neurobiol Lab, Rome, Italy
[3] Univ Roma La Sapienza, IRCCS Fdn Santa Lucia, Rome, Italy
[4] Univ Roma La Sapienza, Dept Human Physiol & Pharmacol, Rome, Italy
[5] Univ Pavia, Univ Ctr Adapt Disorders & Headache, I-27100 Pavia, Italy
[6] Univ Roma La Sapienza, Dept Clin Neurol & ORL, Rome, Italy
[7] Univ Liege, Dept Neurol & Neuroanat, Headache Res Unit, B-4000 Liege, Belgium
关键词
D O I
暂无
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
引用
收藏
页码:149 / 149
页数:1
相关论文
共 50 条
  • [21] A novel ATP1A2 mutation in a case of familial hemiplegic migraine with especially severe attacks
    Martinez, E.
    Moreno, R.
    Lopez-Mesonero, L.
    Ruiz, M.
    Vidriales, I.
    Mulero, P.
    Tellez, N.
    Guerrero, A.
    Telleria, J. J.
    JOURNAL OF HEADACHE AND PAIN, 2014, 15
  • [22] Identification of a novel ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2
    Kaunisto, MA
    Harno, H
    Vanmolkot, KRJ
    Gargus, JJ
    Sun, G
    Liukkonen, E
    Kallela, M
    Van Den Maagdenberg, AMJM
    Frants, RR
    Farkkila, M
    Palotie, A
    Wessman, M
    CEPHALALGIA, 2005, 25 (08) : 676 - 676
  • [23] A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2
    Kaunisto, MA
    Harno, H
    Vanmolkot, KRJ
    Gargus, JJ
    Sun, G
    Hämäläinen, E
    Liukkonen, E
    Kallela, M
    van den Maagdenberg, AMJM
    Frants, RR
    Färkkilä, M
    Palotie, A
    Wessman, M
    NEUROGENETICS, 2004, 5 (02) : 141 - 146
  • [24] A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2
    M. A. Kaunisto
    H. Harno
    K. R. J. Vanmolkot
    J. J. Gargus
    G. Sun
    E. Hämäläinen
    E. Liukkonen
    M. Kallela
    A. M. J. M. van den Maagdenberg
    R. R. Frants
    M. Färkkilä
    A. Palotie
    M. Wessman
    Neurogenetics, 2004, 5 : 141 - 146
  • [25] Alternating hemiplegia of childhood:: No mutations in the second familial hemiplegic migraine gene ATP1A2
    Kors, EE
    Vanmolkot, KRJ
    Haan, J
    Kia, SK
    Stroink, H
    Laan, LAEM
    Gill, DS
    Pascual, J
    van den Maagdenberg, AMJM
    Frants, RR
    Ferrari, MD
    NEUROPEDIATRICS, 2004, 35 (05) : 293 - 296
  • [26] ATP1A2 Mutations in 11 Families With Familial Hemiplegic Migraine
    Riant, Florence
    De Fusco, Maurizio
    Aridon, Paolo
    Ducros, Anne
    Ploton, Claire
    Marchelli, Florence
    Maciazek, Jacqueline
    Bousser, Marie Germaine
    Casari, Giorgio
    Tournier-Lasserve, Elisabeth
    HUMAN MUTATION, 2005, 26 (03) : 281
  • [27] A Chinese Family with Familial Hemiplegic Migraine type 2 Due to a Novel Missense Mutation in ATP1A2
    Zhao, D.
    Meicheng, Z.
    Wenjing, T.
    Yu, S.
    Huan-xian, L.
    HEADACHE, 2018, 58 : 143 - 144
  • [28] A Chinese family with familial hemiplegic migraine type 2 due to a novel missense mutation in ATP1A2
    Tang, Wenjing
    Zhang, Meichen
    Qiu, Enchao
    Kong, Shanshan
    Li, Yingji
    Liu, Huanxian
    Dong, Zhao
    Yu, Shengyuan
    CEPHALALGIA, 2019, 39 (11) : 1382 - 1395
  • [29] Novel missense mutation in the ATP1A2 gene associated with atypical sporadic hemiplegic migraine
    Rispoli, Marianna Gabriella
    Di Stefano, Vincenzo
    Mantuano, Elide
    De Angelis, Maria Vittoria
    BMJ CASE REPORTS, 2019, 12 (10)
  • [30] ATP1A2 gene mutations are not present in two sisters with basilar-type migraine associated with menses
    Cologno, Daniela
    d'Onofrio, Florindo
    Esposito, Teresa
    Gianfrancesco, Fernando
    Petretta, Vittorio
    Casucci, Gerardo
    Frediani, Fabio
    Buzzi, Maria Gabriella
    Bussone, Gennaro
    NEUROLOGICAL SCIENCES, 2008, 29 (02) : 113 - 115