Inherited neuropathies: an update

被引:0
|
作者
Anna Sagnelli
Giuseppe Piscosquito
Davide Pareyson
机构
[1] “C. Besta” Neurological Institute,Clinic of Central and Peripheral Degenerative Neuropathies Unit, Department of Clinical Neurosciences, IRCCS Foundation
来源
Journal of Neurology | 2013年 / 260卷
关键词
Charcot-Marie-Tooth disease; Familial amyloid polyneuropathy; Mitochondrial disease; Tangier disease; Allgrove syndrome; ARSACS;
D O I
暂无
中图分类号
学科分类号
摘要
In this review, progress in hereditary neuropathy research published in the Journal of Neurology over the last 18 months is summarised.
引用
收藏
页码:2684 / 2690
页数:6
相关论文
共 50 条
  • [31] Therapeutic strategies for the inherited neuropathies
    Shy, Michael E.
    NEUROMOLECULAR MEDICINE, 2006, 8 (1-2) : 255 - 278
  • [32] Molecular genetics of inherited neuropathies
    Takashima, Hiroshi
    NEUROSCIENCE RESEARCH, 2006, 55 : S20 - S20
  • [33] DISEASE BURDEN IN INHERITED NEUROPATHIES
    Ramchandren, S.
    Jaiswal, M.
    Bogue, L.
    Kirk, C.
    Dreibelbis, P.
    Shy, M. E.
    JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2015, 20 (02) : 216 - 216
  • [34] Finding the causes of inherited neuropathies
    Scherer, SS
    ARCHIVES OF NEUROLOGY, 2006, 63 (06) : 812 - 816
  • [35] The Schwann cell and the inherited neuropathies
    Marques Jr, W.
    BRAIN PATHOLOGY, 2014, 24 : 28 - 28
  • [36] Therapeutic tools for inherited neuropathies
    Pereon, Y.
    REVUE NEUROLOGIQUE, 2023, 179 (1-2) : 5 - 9
  • [37] Analysis of Inherited Optic Neuropathies
    Lazdinyte, Simona
    Schorderet, Daniel F.
    Schaller, Andre
    Valmaggia, Christophe
    Todorova, Margarita G.
    KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE, 2019, 236 (04) : 451 - 461
  • [38] Therapeutic strategies for the inherited neuropathies
    Michael E. Shy
    NeuroMolecular Medicine, 2006, 8 : 255 - 278
  • [39] Disease mechanisms in inherited neuropathies
    Ueli Suter
    Steven S. Scherer
    Nature Reviews Neuroscience, 2003, 4 : 714 - 726
  • [40] Inherited mitochondrial optic neuropathies
    Yu-Wai-Man, P.
    Griffiths, P. G.
    Hudson, G.
    Chinnery, P. F.
    JOURNAL OF MEDICAL GENETICS, 2009, 46 (03) : 145 - 158