ATP1A2 from gene structure to clinical implications

被引：0
|
作者：
Harder, Aster V. E. [1 ,2 ]
Vijfhuizen, Lisanne S. [1 ]
de Boer, Irene [2 ]
Ferrari, Michel D. [2 ]
Terwindt, Gisela M. [2 ]
van den Maagdenberg, Arn M. J. M. [1 ,2 ]
机构：
[1] Leiden Univ, Med Ctr, Human Genet, Leiden, Netherlands
[2] Leiden Univ, Med Ctr, Neurol, Leiden, Netherlands
来源：
CEPHALALGIA | 2019年 / 39卷
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：
IHC-PO-274
引用
收藏
页码：81 / 82
页数：2
相关论文
共 50 条
  • [31] ATP1A2: a key player in familial hemiplegic migraine
    Blostein, R
    Segall, L
    Gargus, JJ
    [J]. M S-MEDECINE SCIENCES, 2006, 22 (04): : 341 - 343
  • [32] Screening of CACNA1A and ATP1A2 genes in hemiplegic migraine: clinical, genetic, and functional studies
    Carreno, Oriel
    Corominas, Roser
    Angelica Serra, Selma
    Sintas, Celia
    Fernandez-Castillo, Noelia
    Vila-Pueyo, Marta
    Toma, Claudio
    Gene, Gemma G.
    Pons, Roser
    Llaneza, Miguel
    Sobrido, Maria-Jesus
    Grinberg, Daniel
    Angel Valverde, Miguel
    Manuel Fernandez-Fernandez, Jose
    Macaya, Alfons
    Cormand, Bru
    [J]. MOLECULAR GENETICS & GENOMIC MEDICINE, 2013, 1 (04): : 206 - 222
  • [33] Pediatric sporadic hemiplegic migraine (ATP1A2 gene): a case report and brief literature review
    Ghil Schwarz
    Nicoletta Anzalone
    Cristina Baldoli
    Matteo Impellizzeri
    Fabio Minicucci
    Giancarlo Comi
    Bruno Colombo
    [J]. Neurological Sciences, 2018, 39 : 69 - 71
  • [34] Recurrent transient hemiparesis and a novel ATP1A2 mutation
    Stredny, Coral
    Winden, Kellen
    Danehy, Amy
    Robertson, Richard
    Trenor, Cameron
    Rivkin, Michael
    Lehman, Laura
    Bernson-Leung, Miya
    [J]. NEUROLOGY, 2017, 88
  • [35] Expanding the clinical spectrum and functional consequences associated with mutations in the Na+, K+-ATPase pump gene ATP1A2
    Vanmolkot, KRJ
    Dylsad, T
    Stroink, H
    Koenderink, JB
    Kors, EE
    Broos, L
    van den Heuvel, J
    Haan, J
    Frants, RR
    Ferrari, MD
    van den Maagdenberg, AMJM
    [J]. CEPHALALGIA, 2005, 25 (10) : 863 - 863
  • [36] Screening of cacna1a and ATP1A2 genes in hemiplegic migraine: clinical, genetic and functional studies
    Sintas, C.
    Carreno, O.
    Corominas, R.
    Serra, S. A.
    Vila, M.
    Fernandez-Castillo, N.
    Toma, C.
    Pons, R.
    Llaneza, M.
    Sobrido, M. J.
    Grinberg, D.
    Valverde, M. A.
    Fernandez-Fernandez, J. M.
    Macaya, A.
    Cormand, B.
    [J]. JOURNAL OF HEADACHE AND PAIN, 2013, 14
  • [37] Screening of cacna1a and ATP1A2 genes in hemiplegic migraine: clinical, genetic and functional studies
    C Sintas
    O Carreño
    R Corominas
    SA Serra
    M Vila
    N Fernández-Castillo
    C Toma
    R Pons
    M Llaneza
    MJ Sobrido
    D Grinberg
    MA Valverde
    JM Fernández-Fernández
    A Macaya
    B Cormand
    [J]. The Journal of Headache and Pain, 2013, 14
  • [38] Pediatric sporadic hemiplegic migraine (ATP1A2 gene): a case report and brief literature review
    Schwarz, Ghil
    Anzalone, Nicoletta
    Baldoli, Cristina
    Impellizzeri, Matteo
    Minicucci, Fabio
    Comi, Giancarlo
    Colombo, Bruno
    [J]. NEUROLOGICAL SCIENCES, 2018, 39 : S69 - S71
  • [39] HYPOKALAEMIC PERIODIC PARALYSIS DUE TO A NOVEL ATP1A2 MUTATION: A NEW PERIODIC PARALYSIS GENE?
    Matthews, E.
    Zanoteli, E.
    Scalco, R.
    O'Callaghan, B.
    Sud, R.
    McCall, S.
    Bugiardini, E.
    Phadke, R.
    Hanna, M. G.
    Poulsen, H.
    Castenada, M. S.
    Mannikko, R.
    [J]. MUSCLE & NERVE, 2017, 56 : S13 - S14
  • [40] Hypokalaemic periodic paralysis due to a novel ATP1A2 mutation: a new periodic paralysis gene?
    Matthews, E.
    Zanoteli, E.
    Scalco, R. S.
    O'Callaghan, B.
    Sud, R.
    McCall, S.
    Hanna, M. G.
    Castenada, M. Sampedro
    Mannikko, R.
    Poulson, H.
    [J]. NEUROMUSCULAR DISORDERS, 2017, 27 : S33 - S33
12345