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Journal Abstract Search

372 related items for PubMed ID: 21424531

  • 1. The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS gene.
    Snowden JS, Hu Q, Rollinson S, Halliwell N, Robinson A, Davidson YS, Momeni P, Baborie A, Griffiths TD, Jaros E, Perry RH, Richardson A, Pickering-Brown SM, Neary D, Mann DM.
    Acta Neuropathol; 2011 Jul; 122(1):99-110. PubMed ID: 21424531
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  • 3. FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration.
    Urwin H, Josephs KA, Rohrer JD, Mackenzie IR, Neumann M, Authier A, Seelaar H, Van Swieten JC, Brown JM, Johannsen P, Nielsen JE, Holm IE, FReJA Consortium, Dickson DW, Rademakers R, Graff-Radford NR, Parisi JE, Petersen RC, Hatanpaa KJ, White CL, Weiner MF, Geser F, Van Deerlin VM, Trojanowski JQ, Miller BL, Seeley WW, van der Zee J, Kumar-Singh S, Engelborghs S, De Deyn PP, Van Broeckhoven C, Bigio EH, Deng HX, Halliday GM, Kril JJ, Munoz DG, Mann DM, Pickering-Brown SM, Doodeman V, Adamson G, Ghazi-Noori S, Fisher EM, Holton JL, Revesz T, Rossor MN, Collinge J, Mead S, Isaacs AM.
    Acta Neuropathol; 2010 Jul; 120(1):33-41. PubMed ID: 20490813
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  • 4. Expanding the Phenotype of Frontotemporal Lobar Degeneration With FUS-Positive Pathology (FTLD-FUS).
    Chornenka K, Hirsch-Reinshagen V, Perez-Rosendahl M, Feldman H, Segal-Gidan F, Vinters HV, Mackenzie IR.
    J Neuropathol Exp Neurol; 2020 Jul 01; 79(7):809-812. PubMed ID: 32483606
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  • 5. Neuronal intermediate filament inclusion disease may be incorrectly classified as a subtype of FTLD-FUS.
    Bieniek KF, Josephs KA, Lin WL, Dickson DW.
    Free Neuropathol; 2020 Jul 01; 1():. PubMed ID: 34386806
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  • 8. Pathological features of FTLD-FUS in a Japanese population: analyses of nine cases.
    Kobayashi Z, Kawakami I, Arai T, Yokota O, Tsuchiya K, Kondo H, Shimomura Y, Haga C, Aoki N, Hasegawa M, Hosokawa M, Oshima K, Niizato K, Ishizu H, Terada S, Onaya M, Ikeda M, Oyanagi K, Nakano I, Murayama S, Akiyama H, Mizusawa H.
    J Neurol Sci; 2013 Dec 15; 335(1-2):89-95. PubMed ID: 24050818
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  • 9. A comparative clinical, pathological, biochemical and genetic study of fused in sarcoma proteinopathies.
    Lashley T, Rohrer JD, Bandopadhyay R, Fry C, Ahmed Z, Isaacs AM, Brelstaff JH, Borroni B, Warren JD, Troakes C, King A, Al-Saraj S, Newcombe J, Quinn N, Ostergaard K, Schrøder HD, Bojsen-Møller M, Braendgaard H, Fox NC, Rossor MN, Lees AJ, Holton JL, Revesz T.
    Brain; 2011 Sep 15; 134(Pt 9):2548-64. PubMed ID: 21752791
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  • 10. Frontotemporal lobar degeneration: epidemiology, pathology, diagnosis and management.
    Seltman RE, Matthews BR.
    CNS Drugs; 2012 Oct 01; 26(10):841-70. PubMed ID: 22950490
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  • 11. Clinical features of the behavioural variant of frontotemporal dementia that are useful for predicting underlying pathological subtypes of frontotemporal lobar degeneration.
    Kobayashi Z, Arai T, Kawakami I, Yokota O, Hosokawa M, Oshima K, Niizato K, Shiraishi A, Akiyama H, Mizusawa H.
    Psychogeriatrics; 2018 Jul 01; 18(4):307-312. PubMed ID: 30133939
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  • 12. Frontotemporal lobar degeneration: diversity of FTLD lesions.
    Seilhean D, Bielle F, Plu I, Duyckaerts C.
    Rev Neurol (Paris); 2013 Oct 01; 169(10):786-92. PubMed ID: 24035575
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  • 13. FUS pathology in basophilic inclusion body disease.
    Munoz DG, Neumann M, Kusaka H, Yokota O, Ishihara K, Terada S, Kuroda S, Mackenzie IR.
    Acta Neuropathol; 2009 Nov 01; 118(5):617-27. PubMed ID: 19830439
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  • 14. Expression of Fused in sarcoma mutations in mice recapitulates the neuropathology of FUS proteinopathies and provides insight into disease pathogenesis.
    Verbeeck C, Deng Q, Dejesus-Hernandez M, Taylor G, Ceballos-Diaz C, Kocerha J, Golde T, Das P, Rademakers R, Dickson DW, Kukar T.
    Mol Neurodegener; 2012 Oct 10; 7():53. PubMed ID: 23046583
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  • 15. Diffuse argyrophilic grain disease with TDP-43 proteinopathy and neuronal intermediate filament inclusion disease: FTLD with mixed tau, TDP-43 and FUS pathologies.
    Koga S, Murakami A, Soto-Beasley AI, Walton RL, Baker MC, Castanedes-Casey M, Josephs KA, Ross OA, Dickson DW.
    Acta Neuropathol Commun; 2023 Jul 06; 11(1):109. PubMed ID: 37415197
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  • 16. [Frontotemporal dementia: clinical features, genetics, pathogenesis and treatment].
    Rosenmann H, Meiner Z.
    Harefuah; 2013 Nov 06; 152(11):661-6, 687. PubMed ID: 24416825
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  • 17. Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degeneration.
    Rohrer JD, Lashley T, Schott JM, Warren JE, Mead S, Isaacs AM, Beck J, Hardy J, de Silva R, Warrington E, Troakes C, Al-Sarraj S, King A, Borroni B, Clarkson MJ, Ourselin S, Holton JL, Fox NC, Revesz T, Rossor MN, Warren JD.
    Brain; 2011 Sep 06; 134(Pt 9):2565-81. PubMed ID: 21908872
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  • 18. Frontotemporal lobar degeneration: Pathogenesis, pathology and pathways to phenotype.
    Mann DMA, Snowden JS.
    Brain Pathol; 2017 Nov 06; 27(6):723-736. PubMed ID: 28100023
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  • 19. Clinical, genetic and pathological heterogeneity of frontotemporal dementia: a review.
    Seelaar H, Rohrer JD, Pijnenburg YA, Fox NC, van Swieten JC.
    J Neurol Neurosurg Psychiatry; 2011 May 06; 82(5):476-86. PubMed ID: 20971753
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  • 20. Chorea as a clinical feature of the basophilic inclusion body disease subtype of fused-in-sarcoma-associated frontotemporal lobar degeneration.
    Kawakami I, Kobayashi Z, Arai T, Yokota O, Nonaka T, Aoki N, Niizato K, Oshima K, Higashi S, Katsuse O, Hosokawa M, Hasegawa M, Akiyama H.
    Acta Neuropathol Commun; 2016 Apr 04; 4():36. PubMed ID: 27044537
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