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Journal Abstract Search

476 related items for PubMed ID: 21908872

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  • 3. 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; 18(4):307-312. PubMed ID: 30133939
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  • 4. 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; 134(Pt 9):2548-64. PubMed ID: 21752791
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  • 5. Neuropathological fingerprints of survival, atrophy and language in primary progressive aphasia.
    Mesulam MM, Coventry CA, Bigio EH, Sridhar J, Gill N, Fought AJ, Zhang H, Thompson CK, Geula C, Gefen T, Flanagan M, Mao Q, Weintraub S, Rogalski EJ.
    Brain; 2022 Jun 30; 145(6):2133-2148. PubMed ID: 35441216
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  • 7. Motor neuron TDP-43 proteinopathy in progressive supranuclear palsy and corticobasal degeneration.
    Riku Y, Iwasaki Y, Ishigaki S, Akagi A, Hasegawa M, Nishioka K, Li Y, Riku M, Ikeuchi T, Fujioka Y, Miyahara H, Sone J, Hattori N, Yoshida M, Katsuno M, Sobue G.
    Brain; 2022 Aug 27; 145(8):2769-2784. PubMed ID: 35274674
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  • 13. TDP-43 subtypes are associated with distinct atrophy patterns in frontotemporal dementia.
    Rohrer JD, Geser F, Zhou J, Gennatas ED, Sidhu M, Trojanowski JQ, Dearmond SJ, Miller BL, Seeley WW.
    Neurology; 2010 Dec 14; 75(24):2204-11. PubMed ID: 21172843
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  • 14. [Clinicopathological features of sporadic frontotemporal lobar degeneration with TDP-43-positive inclusions].
    Yokota O.
    Rinsho Shinkeigaku; 2010 Nov 14; 50(11):1018-21. PubMed ID: 21921551
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  • 15. Frontotemporal lobar degeneration: diversity of FTLD lesions.
    Seilhean D, Bielle F, Plu I, Duyckaerts C.
    Rev Neurol (Paris); 2013 Oct 14; 169(10):786-92. PubMed ID: 24035575
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  • 16. 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 14; 122(1):99-110. PubMed ID: 21424531
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  • 18. Mixed TDP-43 proteinopathy and tauopathy in frontotemporal lobar degeneration: nine case series.
    Kim EJ, Brown JA, Deng J, Hwang JL, Spina S, Miller ZA, DeMay MG, Valcour V, Karydas A, Ramos EM, Coppola G, Miller BL, Rosen HJ, Seeley WW, Grinberg LT.
    J Neurol; 2018 Dec 14; 265(12):2960-2971. PubMed ID: 30324308
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  • 19. Right temporal degeneration and socioemotional semantics: semantic behavioural variant frontotemporal dementia.
    Younes K, Borghesani V, Montembeault M, Spina S, Mandelli ML, Welch AE, Weis E, Callahan P, Elahi FM, Hua AY, Perry DC, Karydas A, Geschwind D, Huang E, Grinberg LT, Kramer JH, Boxer AL, Rabinovici GD, Rosen HJ, Seeley WW, Miller ZA, Miller BL, Sturm VE, Rankin KP, Gorno-Tempini ML.
    Brain; 2022 Nov 21; 145(11):4080-4096. PubMed ID: 35731122
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  • 20. Redefining the multidimensional clinical phenotypes of frontotemporal lobar degeneration syndromes.
    Murley AG, Coyle-Gilchrist I, Rouse MA, Jones PS, Li W, Wiggins J, Lansdall C, Rodríguez PV, Wilcox A, Tsvetanov KA, Patterson K, Lambon Ralph MA, Rowe JB.
    Brain; 2020 May 01; 143(5):1555-1571. PubMed ID: 32438414
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