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Journal Abstract Search

874 related items for PubMed ID: 27604643

  • 1. Screening of SOD1, FUS and TARDBP genes in patients with amyotrophic lateral sclerosis in central-southern China.
    Hou L, Jiao B, Xiao T, Zhou L, Zhou Z, Du J, Yan X, Wang J, Tang B, Shen L.
    Sci Rep; 2016 Sep 08; 6():32478. PubMed ID: 27604643
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  • 2. Mutation analysis of SOD1, C9orf72, TARDBP and FUS genes in ethnically-diverse Malaysian patients with amyotrophic lateral sclerosis (ALS).
    Edgar S, Ellis M, Abdul-Aziz NA, Goh KJ, Shahrizaila N, Kennerson ML, Ahmad-Annuar A.
    Neurobiol Aging; 2021 Dec 08; 108():200-206. PubMed ID: 34404558
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  • 9. Improving the knowledge of amyotrophic lateral sclerosis genetics: novel SOD1 and FUS variants.
    Bertolin C, D'Ascenzo C, Querin G, Gaiani A, Boaretto F, Salvoro C, Vazza G, Angelini C, Cagnin A, Pegoraro E, Sorarù G, Mostacciuolo ML.
    Neurobiol Aging; 2014 May 08; 35(5):1212.e7-1212.e10. PubMed ID: 24325798
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  • 10. De novo truncating FUS gene mutation as a cause of sporadic amyotrophic lateral sclerosis.
    DeJesus-Hernandez M, Kocerha J, Finch N, Crook R, Baker M, Desaro P, Johnston A, Rutherford N, Wojtas A, Kennelly K, Wszolek ZK, Graff-Radford N, Boylan K, Rademakers R.
    Hum Mutat; 2010 May 08; 31(5):E1377-89. PubMed ID: 20232451
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  • 11. FUS mutations in amyotrophic lateral sclerosis: clinical, pathological, neurophysiological and genetic analysis.
    Blair IP, Williams KL, Warraich ST, Durnall JC, Thoeng AD, Manavis J, Blumbergs PC, Vucic S, Kiernan MC, Nicholson GA.
    J Neurol Neurosurg Psychiatry; 2010 Jun 08; 81(6):639-45. PubMed ID: 19965854
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  • 13. Amyotrophic lateral sclerosis patients with various gene mutations show diverse motor phenotypes and survival in China.
    Jiang Q, Lin J, Wei Q, Yang T, Hou Y, Zhang L, Ou R, Xiao Y, Wang S, Zheng X, Li C, Shang H.
    J Med Genet; 2024 Aug 29; 61(9):839-846. PubMed ID: 38886047
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  • 14. Genetic analysis of amyotrophic lateral sclerosis in the Slovenian population.
    Vrabec K, Koritnik B, Leonardis L, Dolenc-Grošelj L, Zidar J, Smith B, Vance C, Shaw C, Rogelj B, Glavač D, Ravnik-Glavač M.
    Neurobiol Aging; 2015 Mar 29; 36(3):1601.e17-20. PubMed ID: 25585530
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  • 16. TARDBP (TDP-43) sequence analysis in patients with familial and sporadic ALS: identification of two novel mutations.
    Del Bo R, Ghezzi S, Corti S, Pandolfo M, Ranieri M, Santoro D, Ghione I, Prelle A, Orsetti V, Mancuso M, Sorarù G, Briani C, Angelini C, Siciliano G, Bresolin N, Comi GP.
    Eur J Neurol; 2009 Jun 29; 16(6):727-32. PubMed ID: 19236453
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  • 17. Mutations in FUS are the most frequent genetic cause in juvenile sporadic ALS patients of Chinese origin.
    Zou ZY, Liu MS, Li XG, Cui LY.
    Amyotroph Lateral Scler Frontotemporal Degener; 2016 Jun 29; 17(3-4):249-52. PubMed ID: 26972116
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  • 18. Comprehensive analysis of the mutation spectrum in 301 German ALS families.
    Müller K, Brenner D, Weydt P, Meyer T, Grehl T, Petri S, Grosskreutz J, Schuster J, Volk AE, Borck G, Kubisch C, Klopstock T, Zeller D, Jablonka S, Sendtner M, Klebe S, Knehr A, Günther K, Weis J, Claeys KG, Schrank B, Sperfeld AD, Hübers A, Otto M, Dorst J, Meitinger T, Strom TM, Andersen PM, Ludolph AC, Weishaupt JH, German ALS network MND-NET.
    J Neurol Neurosurg Psychiatry; 2018 Aug 29; 89(8):817-827. PubMed ID: 29650794
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  • 19. Genetics of familial Amyotrophic lateral sclerosis.
    Ticozzi N, Tiloca C, Morelli C, Colombrita C, Poletti B, Doretti A, Maderna L, Messina S, Ratti A, Silani V.
    Arch Ital Biol; 2011 Mar 29; 149(1):65-82. PubMed ID: 21412717
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  • 20. Effect of familial clustering in the genetic screening of 235 French ALS families.
    Corcia P, Camu W, Brulard C, Marouillat S, Couratier P, Camdessanché JP, Cintas P, Verschueren A, Soriani MH, Desnuelle C, Fleury MC, Guy N, Cassereau J, Viader F, Pittion-Vouyovitch S, Danel V, Kolev I, Le Masson G, Beltran S, Salachas F, Bernard E, Pradat PF, Blasco H, Lanznaster D, Hergesheimer R, Laumonnier F, Andres CR, Meininger V, Vourc'h P.
    J Neurol Neurosurg Psychiatry; 2021 May 29; 92(5):479-484. PubMed ID: 33408239
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