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
来源：
ANNALS OF NEUROLOGY | 1996年 / 40卷 / 01期
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
  • [1] Is hereditary inclusion body myopathy a glycosylation disease?
    Hinderlich, S
    Eisenberg, I
    Horstkorte, R
    Reutter, W
    Mitrani-Rosenbaum, S
    GLYCOBIOLOGY, 2002, 12 (10) : 643 - 643
  • [2] Hereditary inclusion body myopathy
    Zaremba, Jacek
    Hausmanowa-Petrusewicz, Irena
    AKTUALNOSCI NEUROLOGICZNE, 2005, 5 (04): : 261 - 264
  • [3] Hereditary inclusion body myopathy
    Sievert, M
    Zierz, S
    NERVENHEILKUNDE, 2004, 23 (08) : 454 - 456
  • [4] MOLECULAR MIMICRY BETWEEN CELLULAR PHENOTYPES OF SPORADIC INCLUSION-BODY MYOSITIS, HEREDITARY INCLUSION-BODY MYOPATHY, ALZHEIMERS-DISEASE, AND PRION DISEASES
    ASKANAS, V
    ENGEL, WK
    ANNALS OF NEUROLOGY, 1995, 38 (02) : 282 - 282
  • [5] Distal myopathy with rimmed vacuoles and hereditary inclusion body myopathy
    Nonaka I.
    Noguchi S.
    Nishino I.
    Current Neurology and Neuroscience Reports, 2005, 5 (1) : 61 - 65
  • [6] Hereditary inclusion body myopathy in Bulgarian gypsies
    Tournev, I.
    Cirak, S.
    Herrmann, R.
    Guergueltcheva, V.
    Goebel, H.
    Chandler, D.
    Ishpekova, B.
    Petkov, R.
    Tzekov, H.
    Aneva, L.
    Raychev, R.
    Docheva, P.
    Kalaydjieva, L.
    Voit, T.
    EUROPEAN JOURNAL OF NEUROLOGY, 2005, 12 : 282 - 282
  • [7] Hereditary Inclusion Body Myopathy: A decade of progress
    Huizing, Marjan
    Krasnewich, Donna M.
    BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2009, 1792 (09): : 881 - 887
  • [8] The Proteomic Profile of Hereditary Inclusion Body Myopathy
    Sela, Ilan
    Krentsis, Irit Milman
    Shlomai, Zipora
    Sadeh, Menachem
    Dabby, Ron
    Argov, Zohar
    Ben-Bassat, Hannah
    Mitrani-Rosenbaum, Stella
    PLOS ONE, 2011, 6 (01):
  • [9] Familial inclusion body myopathy with desmin storage
    Fidzianska, A
    Drac, H
    Kaminska, AM
    ACTA NEUROPATHOLOGICA, 1999, 97 (05) : 509 - 514
  • [10] Familial inclusion body myopathy with desmin storage
    Anna Fidziańska
    Hanna Drac
    A. M. Kamińska
    Acta Neuropathologica, 1999, 97 : 509 - 514
12345