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Journal Abstract Search

434 related items for PubMed ID: 17278999

  • 1. Neuropathologic features of frontotemporal lobar degeneration with ubiquitin-positive inclusions with progranulin gene (PGRN) mutations.
    Josephs KA, Ahmed Z, Katsuse O, Parisi JF, Boeve BF, Knopman DS, Petersen RC, Davies P, Duara R, Graff-Radford NR, Uitti RJ, Rademakers R, Adamson J, Baker M, Hutton ML, Dickson DW.
    J Neuropathol Exp Neurol; 2007 Feb; 66(2):142-51. PubMed ID: 17278999
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  • 2. Neuropathologic heterogeneity in HDDD1: a familial frontotemporal lobar degeneration with ubiquitin-positive inclusions and progranulin mutation.
    Behrens MI, Mukherjee O, Tu PH, Liscic RM, Grinberg LT, Carter D, Paulsmeyer K, Taylor-Reinwald L, Gitcho M, Norton JB, Chakraverty S, Goate AM, Morris JC, Cairns NJ.
    Alzheimer Dis Assoc Disord; 2007 Feb; 21(1):1-7. PubMed ID: 17334266
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  • 3. Clinicopathologic correlation in PGRN mutations.
    Davion S, Johnson N, Weintraub S, Mesulam MM, Engberg A, Mishra M, Baker M, Adamson J, Hutton M, Rademakers R, Bigio EH.
    Neurology; 2007 Sep 11; 69(11):1113-21. PubMed ID: 17522386
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  • 5. 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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  • 6. Frontotemporal lobar degeneration with ubiquitin-positive inclusions: a molecular genetic update.
    van der Zee J, Gijselinck I, Pirici D, Kumar-Singh S, Cruts M, Van Broeckhoven C.
    Neurodegener Dis; 2007 Aug 24; 4(2-3):227-35. PubMed ID: 17596717
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  • 7. Frontotemporal lobar degeneration without lobar atrophy.
    Josephs KA, Whitwell JL, Jack CR, Parisi JE, Dickson DW.
    Arch Neurol; 2006 Nov 24; 63(11):1632-8. PubMed ID: 17101834
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  • 8. "Frontotemporoparietal" dementia: clinical phenotype associated with the c.709-1G>A PGRN mutation.
    Moreno F, Indakoetxea B, Barandiaran M, Alzualde A, Gabilondo A, Estanga A, Ruiz J, Ruibal M, Bergareche A, Martí-Massó JF, López de Munain A.
    Neurology; 2009 Oct 27; 73(17):1367-74. PubMed ID: 19858458
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  • 9. Ubiquitin-positive neuronal and tau 2-positive glial inclusions in frontotemporal dementia of motor neuron type.
    Forno LS, Langston JW, Herrick MK, Wilson JD, Murayama S.
    Acta Neuropathol; 2002 Jun 27; 103(6):599-606. PubMed ID: 12012092
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  • 10. Deletion of the progranulin gene in patients with frontotemporal lobar degeneration or Parkinson disease.
    Rovelet-Lecrux A, Deramecourt V, Legallic S, Maurage CA, Le Ber I, Brice A, Lambert JC, Frébourg T, Hannequin D, Pasquier F, Campion D.
    Neurobiol Dis; 2008 Jul 27; 31(1):41-5. PubMed ID: 18479928
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  • 13. 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 27; 28(9):846-55. PubMed ID: 17436289
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  • 16. Progranulin (PGRN) expression in ALS: an immunohistochemical study.
    Irwin D, Lippa CF, Rosso A.
    J Neurol Sci; 2009 Jan 15; 276(1-2):9-13. PubMed ID: 18848708
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  • 17. [Clinico-pathological investigation of two patients with dementia with motor neuron disease].
    Yamamoto R, Iseki E, Murayama N, Minegishi M, Kimura M, Eto K, Arai H, Ohbu S, Hatanaka D, Hino H, Fujisawa K.
    Brain Nerve; 2007 Mar 15; 59(3):263-9. PubMed ID: 17370652
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  • 18. Progranulin: normal function and role in neurodegeneration.
    Eriksen JL, Mackenzie IR.
    J Neurochem; 2008 Jan 15; 104(2):287-97. PubMed ID: 17953663
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  • 19. Late-onset frontotemporal dementia associated with a novel PGRN mutation.
    Lladó A, Sánchez-Valle R, Reñé R, Ezquerra M, Rey MJ, Tolosa E, Ferrer I, Molinuevo JL.
    J Neural Transm (Vienna); 2007 Jan 15; 114(8):1051-4. PubMed ID: 17417739
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  • 20. Progranulin mutations in Dutch familial frontotemporal lobar degeneration.
    Bronner IF, Rizzu P, Seelaar H, van Mil SE, Anar B, Azmani A, Donker Kaat L, Rosso S, Heutink P, van Swieten JC.
    Eur J Hum Genet; 2007 Mar 15; 15(3):369-74. PubMed ID: 17228326
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