The electrophysiological footprint of CACNA1A disorders

被引:0
|
作者
Indelicato, E. [1 ]
Unterberger, I. [1 ]
Eigentler, A. [1 ]
Amprosi, M. [1 ]
Zeiner, F. [1 ]
Haberlandt, E.
Kaml, M. [1 ]
Boesch, S.
机构
[1] Med Univ Innsbruck, Innsbruck, Austria
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
EPR-233
引用
收藏
页码:364 / 364
页数:1
相关论文
共 50 条
  • [41] Related research in the polymorphism of CACNA1A of migraine in the southerners of China
    Fang, Y. N.
    Luo, N.
    JOURNAL OF HEADACHE AND PAIN, 2010, 11 : S64 - S64
  • [42] Phenotype and genotype variability of CACNA1A in a cohort of ataxia in Taiwan
    Fong, P. Y.
    Yeh, T. H.
    Lai, S. C.
    Lu, C. S.
    MOVEMENT DISORDERS, 2016, 31 : S196 - S196
  • [43] Stepwise Developmental Regression Associated With Novel CACNA1A Mutation
    Guerin, Andrea A.
    Feigenbaum, Annette
    Donner, Elizabeth J.
    Yoon, Grace
    PEDIATRIC NEUROLOGY, 2008, 39 (05) : 363 - 364
  • [44] Is benign paroxysmal torticollis related to mutations in the CACNA1A gene?
    Douglass, Laurie M.
    Rosman, N. Paul
    Milunsky, Jeff M.
    NEUROLOGY, 2007, 68 (12) : A47 - A47
  • [45] Investigation of the CACNA1A gene as a candidate for typical migraine susceptibility
    Lea, RA
    Curtain, RP
    Hutchins, C
    Brimage, PJ
    Griffiths, LR
    AMERICAN JOURNAL OF MEDICAL GENETICS, 2001, 105 (08): : 707 - 712
  • [46] Evidence for involvement of the CACNA1A gene in idiopathic generalised epilepsy
    Makoff, A.
    Lai, T.
    Barratt, C.
    Asherson, P.
    Moran, N.
    Nashef, N.
    JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2007, 78 (02): : 215 - 215
  • [47] Concomitant Calcium Channelopathies Involving CACNA1A and CACNA1F: A Case Report and Review of the Literature
    Schaare, Donna
    Sarasua, Sara M.
    Lusk, Laina
    Parthasarathy, Shridhar
    Wang, Liangjiang
    Helbig, Ingo
    Boccuto, Luigi
    GENES, 2023, 14 (02)
  • [48] A novel CACNA1A mutation in a neonate with severe encephalopathy at birth
    Ozdil, Mine
    Eroglu, Arzu
    Gerik-Celebi, Hamide Betul
    ACTA NEUROLOGICA BELGICA, 2024, 124 (02) : 705 - 708
  • [49] Clues from oculomotor phenotype to genotype in CACNA1A channelopathies
    Bostan, Alionka
    DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, 2016, 58 (06): : 539 - 540
  • [50] Characterization of CACNA1A mutations in familial and sporadic hemiplegic migraine
    Ducros, A
    Denier, C
    Joutel, A
    Vahedi, K
    Bousser, MG
    Tournier-Lasserve, E
    NEUROLOGY, 1999, 52 (06) : A273 - A274