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Journal Abstract Search

203 related items for PubMed ID: 15888485

  • 1. Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region.
    Cruts M, Rademakers R, Gijselinck I, van der Zee J, Dermaut B, de Pooter T, de Rijk P, Del-Favero J, van Broeckhoven C.
    Hum Mol Genet; 2005 Jul 01; 14(13):1753-62. PubMed ID: 15888485
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  • 2. Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21.
    Cruts M, Gijselinck I, van der Zee J, Engelborghs S, Wils H, Pirici D, Rademakers R, Vandenberghe R, Dermaut B, Martin JJ, van Duijn C, Peeters K, Sciot R, Santens P, De Pooter T, Mattheijssens M, Van den Broeck M, Cuijt I, Vennekens K, De Deyn PP, Kumar-Singh S, Van Broeckhoven C.
    Nature; 2006 Aug 24; 442(7105):920-4. PubMed ID: 16862115
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  • 3. Progranulin mutations in ubiquitin-positive frontotemporal dementia linked to chromosome 17q21.
    Cruts M, Kumar-Singh S, Van Broeckhoven C.
    Curr Alzheimer Res; 2006 Dec 24; 3(5):485-91. PubMed ID: 17168647
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  • 4. [Clinical, pathological, and genetic characteristics of frontotemporal dementia and parkinsonism linked to chromosome 17 with mutations in the MAPT and PGRN].
    Tsuboi Y.
    Brain Nerve; 2009 Nov 24; 61(11):1285-91. PubMed ID: 19938685
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  • 5. Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM interval.
    Rademakers R, Cruts M, Dermaut B, Sleegers K, Rosso SM, Van den Broeck M, Backhovens H, van Swieten J, van Duijn CM, Van Broeckhoven C.
    Mol Psychiatry; 2002 Nov 24; 7(10):1064-74. PubMed ID: 12476321
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  • 7. A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD.
    van der Zee J, Rademakers R, Engelborghs S, Gijselinck I, Bogaerts V, Vandenberghe R, Santens P, Caekebeke J, De Pooter T, Peeters K, Lübke U, Van den Broeck M, Martin JJ, Cruts M, De Deyn PP, Van Broeckhoven C, Dermaut B.
    Brain; 2006 Apr 24; 129(Pt 4):841-52. PubMed ID: 16495329
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  • 9. Progranulin null mutations in both sporadic and familial frontotemporal dementia.
    Le Ber I, van der Zee J, Hannequin D, Gijselinck I, Campion D, Puel M, Laquerrière A, De Pooter T, Camuzat A, Van den Broeck M, Dubois B, Sellal F, Lacomblez L, Vercelletto M, Thomas-Antérion C, Michel BF, Golfier V, Didic M, Salachas F, Duyckaerts C, Cruts M, Verpillat P, Van Broeckhoven C, Brice A, French Research Network on FTD/FTD-MND.
    Hum Mutat; 2007 Sep 24; 28(9):846-55. PubMed ID: 17436289
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  • 12. The H2 MAPT haplotype is associated with familial frontotemporal dementia.
    Ghidoni R, Signorini S, Barbiero L, Sina E, Cominelli P, Villa A, Benussi L, Binetti G.
    Neurobiol Dis; 2006 May 24; 22(2):357-62. PubMed ID: 16410051
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  • 14. 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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  • 17. The G389R mutation in the MAPT gene presenting as sporadic corticobasal syndrome.
    Rossi G, Marelli C, Farina L, Laurà M, Maria Basile A, Ciano C, Tagliavini F, Pareyson D.
    Mov Disord; 2008 Apr 30; 23(6):892-5. PubMed ID: 18307268
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  • 18. Frontotemporal dementia--Part II. Differential diagnosis, genetics, molecular pathomechanism and pathology.
    Galariotis V, Bódi N, Janka Z, Kálmán J.
    Ideggyogy Sz; 2005 Jul 20; 58(7-8):220-4. PubMed ID: 16173270
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  • 19. From 1997 to 2007: a decade journey through the H1 haplotype on 17q21 chromosome.
    Kalinderi K, Fidani L, Bostantjopoulou S.
    Parkinsonism Relat Disord; 2009 Jan 20; 15(1):2-5. PubMed ID: 18424220
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  • 20. Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17.
    Baker M, Mackenzie IR, Pickering-Brown SM, Gass J, Rademakers R, Lindholm C, Snowden J, Adamson J, Sadovnick AD, Rollinson S, Cannon A, Dwosh E, Neary D, Melquist S, Richardson A, Dickson D, Berger Z, Eriksen J, Robinson T, Zehr C, Dickey CA, Crook R, McGowan E, Mann D, Boeve B, Feldman H, Hutton M.
    Nature; 2006 Aug 24; 442(7105):916-9. PubMed ID: 16862116
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