New forms of hereditary inclusion body myopathy (HIBM) and their genetic spectrum

被引：0
|
作者：
Argov, Z
Sadeh, M
Karpati, G
Eisenberg, I
Tiram, E
MitraniRosenbaum, S
机构：
来源：
NEUROLOGY | 1997年 / 48卷 / 03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：41001 / 41001
页数：1
相关论文
共 50 条
  • [11] Hypoglycosylation of alpha-dystroglycan in patients with hereditary inclusion body myopathy (HIBM) due to GNE mutations
    Rakocevic, G
    Huizing, M
    Sparks, SE
    Mamali, I
    Goldfarb, L
    Krasnewich, D
    Gahl, WA
    Dalakas, MC
    NEUROLOGY, 2004, 62 (07) : A171 - A171
  • [12] Hereditary inclusion body myopathy
    Zaremba, Jacek
    Hausmanowa-Petrusewicz, Irena
    AKTUALNOSCI NEUROLOGICZNE, 2005, 5 (04): : 261 - 264
  • [13] Hereditary inclusion body myopathy
    Sievert, M
    Zierz, S
    NERVENHEILKUNDE, 2004, 23 (08) : 454 - 456
  • [14] Hereditary inclusion body myopathy - The Middle Eastern genetic cluster
    Argov, Z
    Eisenberg, L
    Grabov-Nardini, G
    Sadeh, M
    Wirguin, I
    Soffer, D
    Mitrani-Rosenbaum, S
    NEUROLOGY, 2003, 60 (09) : 1519 - 1523
  • [15] A non-viral, GNE-lipoplex treatment to correct sialylation defects in hereditary inclusion body myopathy (HIBM)
    Yardeni, T.
    Manoli, I.
    Ciccone, C.
    Hoogstraten-Miller, S.
    Darvish, D.
    Anikster, Y.
    Maples, P.
    Jay, C. M.
    Gahl, W. A.
    Nemunaitis, J.
    Huizing, M.
    NEUROMUSCULAR DISORDERS, 2010, 20 (9-10) : 620 - 621
  • [16] Preclinical Assessment of wt GNE Gene Plasmid for Management of Hereditary Inclusion Body Myopathy 2 (HIBM2)
    Jay, Chris
    Nemunaitis, Gregory
    Nemunaitis, John
    Senzer, Neil
    Hinderlich, Stephan
    Darvish, Daniel
    Ogden, Julie
    Eager, John
    Tong, Alex
    Maples, Phillip B.
    GENE REGULATION AND SYSTEMS BIOLOGY, 2008, 2 : 243 - 252
  • [17] A phase 1 safety and pharmacokinetic study of sialic acid-extended release tablets in patients with Hereditary Inclusion Body Myopathy (HIBM or GNE myopathy)
    Kakkis, E.
    Maurer, M.
    Shah, P.
    Donikyan, M.
    Ahmed, R.
    NEUROMUSCULAR DISORDERS, 2012, 22 (9-10) : 850 - 850
  • [18] Physical and transcriptional map of the hereditary inclusion body myopathy (HIBM) locus on chromosome 9p12-p13.
    Eisenberg, I
    Hochner, H
    Shemesh, M
    Levi, T
    Potikha, T
    Barash, M
    Grabov, G
    Sadeh, M
    Argov, Z
    Jackson, CL
    Mitrani-Rosenbaum, S
    AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (04) : 611 - 611
  • [19] 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
  • [20] Prevalence of GNE p.M712T and hereditary inclusion body myopathy (HIBM) in Sangesar population of Northern Iran
    Khademian, H.
    Mehravar, E.
    Urtizberea, J. A.
    Sagoo, S.
    Sandoval, L.
    Carbajo, R.
    Darvish, B.
    Valles-Ayoub, Y.
    Darvish, D.
    CLINICAL GENETICS, 2013, 84 (06) : 589 - 592
12345