Recurrent transient hemiparesis and a novel ATP1A2 mutation

被引:0
|
作者
Stredny, Coral [1 ]
Winden, Kellen [1 ]
Danehy, Amy [2 ]
Robertson, Richard [2 ]
Trenor, Cameron [3 ,4 ]
Rivkin, Michael [1 ,2 ,4 ,5 ]
Lehman, Laura [1 ,4 ]
Bemson-Leung, Miya [1 ]
机构
[1] Dept Neurol, Boston, MA USA
[2] Dept Radiol, Boston, MA USA
[3] Div Hematol Oncol, Boston, MA USA
[4] Stroke & Cerebrovasc Ctr, Boston, MA USA
[5] Boston Childrens Hosp, Dept Psychiat, Boston, MA USA
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
P3.220
引用
收藏
页数:2
相关论文
共 50 条
  • [1] 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
  • [2] Sporadic hemiplegic migraine associated with a novel mutation in ATP1A2
    Freilinger, T. M.
    Popovici, M.
    Tavraz, N.
    Friedrich, T.
    Dichgans, M.
    [J]. CEPHALALGIA, 2006, 26 (11) : 1365 - 1365
  • [3] A novel ATP1A2 mutation in a family with FHM type II
    Pierelli, F
    Grieco, GS
    Pauri, F
    Pirro, C
    Fiermonte, G
    Ambrosini, A
    Costa, A
    Buzzi, MG
    Valoppi, M
    Caltagirone, C
    Nappi, G
    Santorelli, FM
    [J]. CEPHALALGIA, 2006, 26 (03) : 324 - 328
  • [4] A novel ATP1A2 mutation in a familial hemiplegic migraine with cognitive impairment
    Chagot, C.
    Frismand, S.
    Riant, F.
    Tournier-Lasserve, E.
    Tyvaert, L.
    [J]. EUROPEAN JOURNAL OF NEUROLOGY, 2016, 23 : 379 - 379
  • [5] A novel mutation in the amino terminus of ATP1A2 associated to hemiplegic migraine
    Gallanti, A.
    Tonelli, A.
    Cardin, V.
    Airoldi, G.
    Redaelli, F.
    Bresolin, N.
    Bassi, M. T.
    [J]. NEUROLOGICAL SCIENCES, 2007, 28 : S243 - S243
  • [6] A novel ATP1A2 gene mutation in familial hemiplegic migraine and epilepsy
    Costa, Cinzia
    Prontera, Paolo
    Sarchielli, Paola
    Tonelli, Alessandra
    Bassi, Maria Teresa
    Cupini, Letizia Maria
    Caproni, Stefano
    Siliquini, Sabrina
    Donti, Emilio
    Calabresi, Paolo
    [J]. CEPHALALGIA, 2014, 34 (01) : 68 - 72
  • [7] A novel mutation in the ATP1A2 gene causes alternating hemiplegia of childhood
    Bassi, MT
    Bresolin, N
    Tonelli, A
    Nazos, K
    Crippa, F
    Baschirotto, C
    Zucca, C
    Bersano, A
    Dolcetta, D
    Boneschi, FM
    Barone, V
    Casari, G
    [J]. JOURNAL OF MEDICAL GENETICS, 2004, 41 (08) : 621 - 628
  • [8] Alternating hemiplegia of childhood or familial hemiplegic migraine?:: A novel ATP1A2 mutation
    Swoboda, KJ
    Kanavakis, E
    Xaidara, A
    Johnson, JE
    Leppert, MF
    Schlesinger-Massart, MB
    Ptacek, LJ
    Silver, K
    Youroukos, S
    [J]. ANNALS OF NEUROLOGY, 2004, 55 (06) : 884 - 887
  • [9] A Case of Familial Hemiplegic Migraine Associated With a Novel ATP1A2 Gene Mutation
    De Cunto, Angela
    Bensa, Marco
    Tonelli, Alessandra
    [J]. PEDIATRIC NEUROLOGY, 2012, 47 (02) : 133 - 136
  • [10] 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
    [J]. JOURNAL OF HEADACHE AND PAIN, 2021, 22 (01):