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Journal Abstract Search

224 related items for PubMed ID: 16008820

  • 1. A new family with frontotemporal dementia with intronic 10+3 splice site mutation in the tau gene: neuropathology and molecular effects.
    Neumann M, Mittelbronn M, Simon P, Vanmassenhove B, de Silva R, Lees A, Klapp J, Meyermann R, Kretzschmar HA.
    Neuropathol Appl Neurobiol; 2005 Aug; 31(4):362-73. PubMed ID: 16008820
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  • 2. Variable phenotypic expression and extensive tau pathology in two families with the novel tau mutation L315R.
    van Herpen E, Rosso SM, Serverijnen LA, Yoshida H, Breedveld G, van de Graaf R, Kamphorst W, Ravid R, Willemsen R, Dooijes D, Majoor-Krakauer D, Kros JM, Crowther RA, Goedert M, Heutink P, van Swieten JC.
    Ann Neurol; 2003 Nov; 54(5):573-81. PubMed ID: 14595646
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  • 3. The L266V tau mutation is associated with frontotemporal dementia and Pick-like 3R and 4R tauopathy.
    Hogg M, Grujic ZM, Baker M, Demirci S, Guillozet AL, Sweet AP, Herzog LL, Weintraub S, Mesulam MM, LaPointe NE, Gamblin TC, Berry RW, Binder LI, de Silva R, Lees A, Espinoza M, Davies P, Grover A, Sahara N, Ishizawa T, Dickson D, Yen SH, Hutton M, Bigio EH.
    Acta Neuropathol; 2003 Oct; 106(4):323-36. PubMed ID: 12883828
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  • 5. Frontotemporal dementia with novel tau pathology and a Glu342Val tau mutation.
    Lippa CF, Zhukareva V, Kawarai T, Uryu K, Shafiq M, Nee LE, Grafman J, Liang Y, St George-Hyslop PH, Trojanowski JQ, Lee VM.
    Ann Neurol; 2000 Dec; 48(6):850-8. PubMed ID: 11117541
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  • 7. Search for a mutation in the tau gene in a Swiss family with frontotemporal dementia.
    Savioz A, Kövari E, Anastasiu R, Rossier C, Saini K, Bouras C, Leuba G.
    Exp Neurol; 2000 Jan; 161(1):330-5. PubMed ID: 10683298
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  • 9. Contrasting genotypes of the tau gene in two phenotypically distinct patients with P301L mutation of frontotemporal dementia and parkinsonism linked to chromosome 17.
    Kobayashi T, Mori H, Okuma Y, Dickson DW, Cookson N, Tsuboi Y, Motoi Y, Tanaka R, Miyashita N, Anno M, Narabayashi H, Mizuno Y.
    J Neurol; 2002 Jun; 249(6):669-75. PubMed ID: 12111297
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  • 15. A novel mutation at position +12 in the intron following exon 10 of the tau gene in familial frontotemporal dementia (FTD-Kumamoto).
    Yasuda M, Takamatsu J, D'Souza I, Crowther RA, Kawamata T, Hasegawa M, Hasegawa H, Spillantini MG, Tanimukai S, Poorkaj P, Varani L, Varani G, Iwatsubo T, Goedert M, Schellenberg DG, Tanaka C.
    Ann Neurol; 2000 Apr; 47(4):422-9. PubMed ID: 10762152
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  • 16. [Frontotemporal dementia: tau mutations, deposition, and molecular mechanisms of neuronal cell death].
    Hasegawa M.
    Rinsho Shinkeigaku; 2004 Nov; 44(11):879-81. PubMed ID: 15651320
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  • 17. A novel mutation (K317M) in the MAPT gene causes FTDP and motor neuron disease.
    Zarranz JJ, Ferrer I, Lezcano E, Forcadas MI, Eizaguirre B, Atarés B, Puig B, Gómez-Esteban JC, Fernández-Maiztegui C, Rouco I, Pérez-Concha T, Fernández M, Rodríguez O, Rodríguez-Martínez AB, de Pancorbo MM, Pastor P, Pérez-Tur J.
    Neurology; 2005 May 10; 64(9):1578-85. PubMed ID: 15883319
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  • 18. Tau is a candidate gene for chromosome 17 frontotemporal dementia.
    Poorkaj P, Bird TD, Wijsman E, Nemens E, Garruto RM, Anderson L, Andreadis A, Wiederholt WC, Raskind M, Schellenberg GD.
    Ann Neurol; 1998 Jun 10; 43(6):815-25. PubMed ID: 9629852
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  • 19. A non-DM1, non-DM2 multisystem myotonic disorder with frontotemporal dementia: phenotype and suggestive mapping of the DM3 locus to chromosome 15q21-24.
    Le Ber I, Martinez M, Campion D, Laquerrière A, Bétard C, Bassez G, Girard C, Saugier-Veber P, Raux G, Sergeant N, Magnier P, Maisonobe T, Eymard B, Duyckaerts C, Delacourte A, Frebourg T, Hannequin D.
    Brain; 2004 Sep 10; 127(Pt 9):1979-92. PubMed ID: 15215218
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  • 20. A novel L266V mutation of the tau gene causes frontotemporal dementia with a unique tau pathology.
    Kobayashi T, Ota S, Tanaka K, Ito Y, Hasegawa M, Umeda Y, Motoi Y, Takanashi M, Yasuhara M, Anno M, Mizuno Y, Mori H.
    Ann Neurol; 2003 Jan 10; 53(1):133-7. PubMed ID: 12509859
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