Iron accumulation in syndromes of neurodegeneration with brain iron accumulation 1 and 2: causative or consequential?

被引:30
作者
Schneider, S. A. [2 ]
Hardy, J.
Bhatia, K. P. [1 ]
机构
[1] UCL, Sobell Dept, Inst Neurol, London WC1N 3BG, England
[2] Univ Lubeck, Dept Neurol, Schilling Dept Clin & Mol Neurogenet, Lubeck, Germany
基金
英国医学研究理事会;
关键词
HALLERVORDEN-SPATZ-SYNDROME; THE-TIGER SIGN; PHOSPHOLIPASE A(2); DISEASE; MUTATION; PLA2G6; DISORDERS;
D O I
10.1136/jnnp.2008.169953
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:589 / 590
页数:2
相关论文
共 21 条
  • [1] The eye-of-the-tiger sign is not a reliable disease marker for Hallervorden-Spatz syndrome
    Baumeister, FAM
    Auer, DP
    Hörtnagel, K
    Freisinger, P
    Meitinger, T
    [J]. NEUROPEDIATRICS, 2005, 36 (03) : 221 - 222
  • [2] BOKRYSHA N, 2008, MULT SCLER, V14, P602
  • [3] INHIBITION OF AUTOIMMUNE NEUROPATHOLOGICAL PROCESS BY TREATMENT WITH AN IRON-CHELATING AGENT
    BOWERN, N
    RAMSHAW, IA
    CLARK, IA
    DOHERTY, PC
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1984, 160 (05) : 1532 - 1543
  • [4] Emerging pathways in genetic Parkinson's disease: Potential role of ceramide metabolism in Lewy body disease
    Bras, Jose
    Singleton, Andrew
    Cookson, Mark R.
    Hardy, John
    [J]. FEBS JOURNAL, 2008, 275 (23) : 5767 - 5773
  • [5] Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease
    Curtis, ARJ
    Fey, C
    Morris, CM
    Bindoff, LA
    Ince, PG
    Chinnery, PF
    Coulthard, A
    Jackson, MJ
    Jackson, AP
    McHale, DP
    Hay, D
    Barker, WA
    Markham, AF
    Bates, D
    Curtis, A
    Burn, J
    [J]. NATURE GENETICS, 2001, 28 (04) : 350 - 354
  • [6] Gerlach M, 2006, J NEURAL TRANSM-SUPP, P133
  • [7] Gregory A, 2005, FOLIA NEUROPATHOL, V43, P286, DOI 10.1016/B978-0-444-63233-3.00019-1
  • [8] THE EFFECT OF AGE ON THE NON-HAEMIN IRON IN THE HUMAN BRAIN
    HALLGREN, B
    SOURANDER, P
    [J]. JOURNAL OF NEUROCHEMISTRY, 1958, 3 (01) : 41 - 51
  • [9] Genetic, clinical, and radiographic delineation of Hallervorden-Spatz syndrome.
    Hayflick, SJ
    Westaway, SK
    Levinson, B
    Zhou, B
    Johnson, MA
    Ching, KHL
    Gitschier, J
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (01) : 33 - 40
  • [10] PLA2G6 mutation underlies infantile neuroaxonal dystrophy
    Khateeb, Shareef
    Flusser, Hagit
    Ofir, Rivka
    Shelef, Ilan
    Narkis, Ginat
    Vardi, Gideon
    Shorer, Zamir
    Levy, Rachel
    Galil, Aharon
    Elbedour, Khalil
    Birk, Ohad S.
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2006, 79 (05) : 942 - 948