ALS and FTD: two sides of the same coin?

被引：8
作者：
Andersen, Peter M. [1 ]
机构：
[1] Umea Univ, Dept Clin Neurosci, SE-90185 Umea, Sweden
来源：
LANCET NEUROLOGY | 2013年 / 12卷 / 10期
关键词：
AMYOTROPHIC-LATERAL-SCLEROSIS; REPEAT EXPANSION; CAG REPEAT; MOSAICISM; DISEASE; COHORT;
D O I：
10.1016/S1474-4422(13)70218-7
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：937 / 938
页数：2
相关论文
共 10 条
  • [1] Clinical genetics of amyotrophic lateral sclerosis: what do we really know?
    Andersen, Peter M.
    Al-Chalabi, Ammar
    [J]. NATURE REVIEWS NEUROLOGY, 2011, 7 (11) : 603 - 615
  • [2] Pattern of ubiquilin pathology in ALS and FTLD indicates presence of C9ORF72 hexanucleotide expansion
    Brettschneider, Johannes
    Van Deerlin, Vivianna M.
    Robinson, John L.
    Kwong, Linda
    Lee, Edward B.
    Ali, Yousuf O.
    Safren, Nathaniel
    Monteiro, Mervyn J.
    Toledo, Jon B.
    Elman, Lauren
    McCluskey, Leo
    Irwin, David J.
    Grossman, Murray
    Molina-Porcel, Laura
    Lee, Virginia M. -Y.
    Trojanowski, John Q.
    [J]. ACTA NEUROPATHOLOGICA, 2012, 123 (06) : 825 - 839
  • [3] Byrne S, 2012, LANCET NEUROL, V11, P232, DOI 10.1016/S1474-4422(12)70014-5
  • [4] Cancel G, 1998, HUM MUTAT, V11, P23, DOI 10.1002/(SICI)1098-1004(1998)11:1<23::AID-HUMU4>3.0.CO
  • [5] 2-M
  • [6] Charcot JM, 1881, LECT DIS NERVOUS S 2, V2
  • [7] Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS
    DeJesus-Hernandez, Mariely
    Mackenzie, Ian R.
    Boeve, Bradley F.
    Boxer, Adam L.
    Baker, Matt
    Rutherford, Nicola J.
    Nicholson, Alexandra M.
    Finch, NiCole A.
    Flynn, Heather
    Adamson, Jennifer
    Kouri, Naomi
    Wojtas, Aleksandra
    Sengdy, Pheth
    Hsiung, Ging-Yuek R.
    Karydas, Anna
    Seeley, William W.
    Josephs, Keith A.
    Coppola, Giovanni
    Geschwind, Daniel H.
    Wszolek, Zbigniew K.
    Feldman, Howard
    Knopman, David S.
    Petersen, Ronald C.
    Miller, Bruce L.
    Dickson, Dennis W.
    Boylan, Kevin B.
    Graff-Radford, Neill R.
    Rademakers, Rosa
    [J]. NEURON, 2011, 72 (02) : 245 - 256
  • [8] A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study
    Gijselinck, Ilse
    Van Langenhove, Tim
    van der Zee, Julie
    Sleegers, Kristel
    Philtjens, Stephanie
    Kleinberger, Gernot
    Janssens, Jonathan
    Bettens, Karolien
    Van Cauwenberghe, Caroline
    Pereson, Sandra
    Engelborghs, Sebastiaan
    Sieben, Anne
    De Jonghe, Peter
    Vandenberghe, Rik
    Santens, Patrick
    De Bleecker, Jan
    Maes, Githa
    Baumer, Veerle
    Dillen, Lubina
    Joris, Geert
    Cuijt, Ivy
    Corsmit, Ellen
    Elinck, Ellen
    Van Dongen, Jasper
    Vermeulen, Steven
    Van den Broeck, Marleen
    Vaerenberg, Carolien
    Mattheijssens, Maria
    Peeters, Karin
    Robberecht, Wim
    Cras, Patrick
    Martin, Jean-Jacques
    De Deyn, Peter P.
    Cruts, Marc
    Van Broeckhoven, Christine
    [J]. LANCET NEUROLOGY, 2012, 11 (01) : 54 - 65
  • [9] SOMATIC AND GONADAL MOSAICISM OF THE HUNTINGTON DISEASE GENE CAG REPEAT IN BRAIN AND SPERM
    TELENIUS, H
    KREMER, B
    GOLDBERG, YP
    THEILMANN, J
    ANDREW, SE
    ZEISLER, T
    ADAM, S
    GREENBERG, C
    IVES, EJ
    CLARKE, LA
    HAYDEN, MR
    [J]. NATURE GENETICS, 1994, 6 (04) : 409 - 414
  • [10] van Blitterswijk M, 2013, LANCET NEUROL, DOI DOI 10.1016/51474-4422(13)70210-2
1