Pattern of brain involvement myotonic dystrophy type 1 (DM1) versus type 2 (DM2)

被引：0
|
作者：
Angelini, Corrado
Ferrati, Chiara
Romeo, Vincenzo
Ermani, Mario
机构：
来源：
NEUROLOGY | 2008年 / 70卷 / 11期
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：A306 / A306
页数：1
相关论文
共 50 条
  • [21] Effects of IPLEX™ in myotonic dystrophy type 1 (DM1)
    Heatwole, Chad R.
    Martens, William
    Quinn, Christine
    Hilbert, James
    Pandya, Shree
    Jackson, Carlayne
    Thornton, Charles
    Moxley, Richard
    NEUROLOGY, 2007, 68 (12) : A404 - A405
  • [22] Strategies for treating myotonic dystrophy type 1 (DM1)
    Thornton, C.
    NEUROMUSCULAR DISORDERS, 2018, 28 : S1 - S1
  • [23] Myotonic dystrophy type 2 (DM2) in Minnesota.
    Day, J
    Liquori, C
    Johnson, C
    Durand, A
    Ranum, L
    AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (04) : 333 - 333
  • [24] Myotonic dystrophy type 1 (DM1) infant and autism spectrum
    不详
    M S-MEDECINE SCIENCES, 2015, 31 : 33 - 33
  • [25] Transgenic mouse models for myotonic dystrophy type 1 (DM1)
    Wansink, DG
    Wieringa, B
    CYTOGENETIC AND GENOME RESEARCH, 2003, 100 (1-4) : 230 - 242
  • [26] Predictors of dysphagia and aspiration in myotonic dystrophy type 1 (DM1)
    Allen, J.
    Ramdharry, G.
    Astin, R.
    Turner, C.
    Smith, C.
    NEUROMUSCULAR DISORDERS, 2021, 31 : S119 - S119
  • [27] Alternative splicing alterations of Ca2+handling genes are associated with Ca2+signal dysregulation in myotonic dystrophy type 1 ( DM1) and type 2 ( DM2) myotubes
    Santoro, M.
    Piacentini, R.
    Masciullo, M.
    Bianchi, M. L. E.
    Modoni, A.
    Podda, M. V.
    Ricci, E.
    Silvestri, G.
    Grassi, C.
    NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 2014, 40 (04) : 464 - 476
  • [28] Myotonic dystrophy type 2 (DM2) may be misdiagnosed as fibromyalgia
    Suominen, T.
    Auvinen, S.
    Hannonen, P.
    Kontula, K.
    Krahe, R.
    Udd, B.
    NEUROMUSCULAR DISORDERS, 2007, 17 (9-10) : 858 - 859
  • [29] Gene expression analysis in myotonic dystrophy: Indications for a common molecular pathogenic pathway in DM1 and DM2
    Botta, Annalisa
    Vallo, Laura
    Rinaldi, Fabrizio
    Bonifazi, Emanuela
    Amati, Francesca
    Biancolella, Michela
    Gambardella, Stefano
    Mancinelli, Enzo
    Angelini, Corrado
    Meola, Giovanni
    Novelli, Giuseppe
    GENE EXPRESSION, 2007, 13 (06): : 339 - 351
  • [30] Cerebrospinal fluid (CSF) tau and amyloid beta42 (Aβ42) protein abnormalities correlate with executive dysfunction in myotonic dystrophy type 1 (DM1) and type 2 (DM2)
    Sansone, Valeria
    Gandossini, Sandra
    Milanese, San Donato
    Galimberti, Daniela
    Fenoglio, Chiara
    Cotelli, Maria
    Calabria, Marco
    Scarpini, Elio
    Meola, Giovanni
    NEUROLOGY, 2008, 70 (11) : A306 - A306
12345