Is hereditary inclusion body myopathy a ''familial prion disease''?

被引:1
|
作者
Cervenakova, L [1 ]
Sivakumar, K [1 ]
Nagle, J [1 ]
Dalakas, MC [1 ]
Goldfarb, LG [1 ]
机构
[1] NINCDS,MED NEUROL BRANCH,NIH,BETHESDA,MD 20892
关键词
D O I
10.1002/ana.410400122
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:128 / 128
页数:1
相关论文
共 50 条
  • [21] PHENOTYPIC HETEROGENEITY IN FAMILIAL INCLUSION-BODY MYOPATHY
    NEUFELD, MY
    SADEH, M
    ASSA, B
    KUSHNIR, M
    KORCZYN, AD
    MUSCLE & NERVE, 1995, 18 (05) : 546 - 548
  • [23] Proteomic analysis of myotubes from hereditary inclusion body myopathy
    Mitrani-Rosenbaurn, S.
    Salama, I.
    Milman, I.
    Shlomai, Z.
    Dagan, A.
    Ben, Bassat H.
    NEUROMUSCULAR DISORDERS, 2007, 17 (9-10) : 851 - 852
  • [24] The hereditary inclusion body myopathy enigma and its future therapy
    Zohar Argov
    Stella Mitrani-Rosenbaum
    Neurotherapeutics, 2008, 5 : 633 - 637
  • [25] The hereditary inclusion body myopathy enigma and its future therapy
    Argov, Zohar
    Mitrani-Rosenbaum, Stella
    NEUROTHERAPEUTICS, 2008, 5 (04) : 633 - 637
  • [26] Multiple mitochondrial DNA deletions in hereditary inclusion body myopathy
    Jansson, M
    Darin, N
    Kyllerman, M
    Martinsson, T
    Wahlström, J
    Oldfors, A
    ACTA NEUROPATHOLOGICA, 2000, 100 (01) : 23 - 28
  • [27] CLINICAL AND ELECTROMYOGRAPHIC FINDINGS IN PATIENTS WITH HEREDITARY INCLUSION BODY MYOPATHY
    Kazamel, Mohamed
    Sorenson, Eric
    Milone, Margherita
    MUSCLE & NERVE, 2014, 50 (04) : 669 - 669
  • [28] Multiple mitochondrial DNA deletions in hereditary inclusion body myopathy
    Monica Jansson
    Niklas Darin
    Mårten Kyllerman
    Tommy Martinsson
    Jan Wahlström
    A. Oldfors
    Acta Neuropathologica, 2000, 100 : 23 - 28
  • [29] Hereditary inclusion body myopathy and frontotemporal dementia in one family
    Jamrozik, Z.
    Kaliszek, A.
    Bojakowski, J.
    Kaminska, A.
    Kwiecinski, H.
    EUROPEAN JOURNAL OF NEUROLOGY, 2004, 11 : 36 - 36
  • [30] Muscle sonography in six patients with hereditary inclusion body myopathy
    Ronald S. Adler
    Giovanna Garolfalo
    Stephen Paget
    Lawrence Kagen
    Skeletal Radiology, 2008, 37 : 43 - 48