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Journal Abstract Search

875 related items for PubMed ID: 27604643

  • 41. De novo nonsense mutation of the FUS gene in an apparently familial amyotrophic lateral sclerosis case.
    Calvo A, Moglia C, Canosa A, Brunetti M, Barberis M, Traynor BJ, Carrara G, Valentini C, Restagno G, Chiò A.
    Neurobiol Aging; 2014 Jun; 35(6):1513.e7-11. PubMed ID: 24439481
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  • 42. From Mouse Models to Human Disease: An Approach for Amyotrophic Lateral Sclerosis.
    Alrafiah AR.
    In Vivo; 2018 Jun; 32(5):983-998. PubMed ID: 30150420
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  • 43. Amyotrophic lateral sclerosis-frontotemporal lobar dementia in 3 families with p.Ala382Thr TARDBP mutations.
    Chiò A, Calvo A, Moglia C, Restagno G, Ossola I, Brunetti M, Montuschi A, Cistaro A, Ticca A, Traynor BJ, Schymick JC, Mutani R, Marrosu MG, Murru MR, Borghero G.
    Arch Neurol; 2010 Aug; 67(8):1002-9. PubMed ID: 20697052
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  • 44. De novo FUS mutations are the most frequent genetic cause in early-onset German ALS patients.
    Hübers A, Just W, Rosenbohm A, Müller K, Marroquin N, Goebel I, Högel J, Thiele H, Altmüller J, Nürnberg P, Weishaupt JH, Kubisch C, Ludolph AC, Volk AE.
    Neurobiol Aging; 2015 Nov; 36(11):3117.e1-3117.e6. PubMed ID: 26362943
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  • 46. Screening for TARDBP mutations in Japanese familial amyotrophic lateral sclerosis.
    Kamada M, Maruyama H, Tanaka E, Morino H, Wate R, Ito H, Kusaka H, Kawano Y, Miki T, Nodera H, Izumi Y, Kaji R, Kawakami H.
    J Neurol Sci; 2009 Sep 15; 284(1-2):69-71. PubMed ID: 19411082
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  • 47. Analysis of SOD1 mutations in a Chinese population with amyotrophic lateral sclerosis: a case-control study and literature review.
    Wei Q, Zhou Q, Chen Y, Ou R, Cao B, Xu Y, Yang J, Shang HF.
    Sci Rep; 2017 Mar 14; 7():44606. PubMed ID: 28291249
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  • 48. Mutations in FUS cause FALS and SALS in French and French Canadian populations.
    Belzil VV, Valdmanis PN, Dion PA, Daoud H, Kabashi E, Noreau A, Gauthier J, S2D team, Hince P, Desjarlais A, Bouchard JP, Lacomblez L, Salachas F, Pradat PF, Camu W, Meininger V, Dupré N, Rouleau GA.
    Neurology; 2009 Oct 13; 73(15):1176-9. PubMed ID: 19741216
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  • 51. Lymphoblastoid cell lines as a model to understand amyotrophic lateral sclerosis disease mechanisms.
    Pansarasa O, Bordoni M, Drufuca L, Diamanti L, Sproviero D, Trotti R, Bernuzzi S, La Salvia S, Gagliardi S, Ceroni M, Cereda C.
    Dis Model Mech; 2018 Mar 26; 11(3):. PubMed ID: 29419416
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  • 57. Unveiling the SOD1-mediated ALS phenotype: insights from a comprehensive meta-analysis.
    Domi T, Schito P, Sferruzza G, Russo T, Pozzi L, Agosta F, Carrera P, Riva N, Filippi M, Quattrini A, Falzone YM.
    J Neurol; 2024 Mar 26; 271(3):1342-1354. PubMed ID: 37930481
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  • 58. Novel FUS mutation in patients with sporadic amyotrophic lateral sclerosis and corticobasal degeneration.
    Nagayama S, Minato-Hashiba N, Nakata M, Kaito M, Nakanishi M, Tanaka K, Arai M, Akiyama H, Matsui M.
    J Clin Neurosci; 2012 Dec 26; 19(12):1738-9. PubMed ID: 22999566
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  • 59. Extensive genetics of ALS: a population-based study in Italy.
    Chiò A, Calvo A, Mazzini L, Cantello R, Mora G, Moglia C, Corrado L, D'Alfonso S, Majounie E, Renton A, Pisano F, Ossola I, Brunetti M, Traynor BJ, Restagno G, PARALS.
    Neurology; 2012 Nov 06; 79(19):1983-9. PubMed ID: 23100398
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