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509 related items for PubMed ID: 18703462

  • 1. Distinct genetic forms of frontotemporal dementia.
    Seelaar H, Kamphorst W, Rosso SM, Azmani A, Masdjedi R, de Koning I, Maat-Kievit JA, Anar B, Donker Kaat L, Breedveld GJ, Dooijes D, Rozemuller JM, Bronner IF, Rizzu P, van Swieten JC.
    Neurology; 2008 Oct 14; 71(16):1220-6. PubMed ID: 18703462
    [Abstract] [Full Text] [Related]

  • 2. 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 14; 28(9):846-55. PubMed ID: 17436289
    [Abstract] [Full Text] [Related]

  • 3. The molecular basis of frontotemporal dementia.
    Neumann M, Tolnay M, Mackenzie IR.
    Expert Rev Mol Med; 2009 Jul 29; 11():e23. PubMed ID: 19638255
    [Abstract] [Full Text] [Related]

  • 4. Mutations in progranulin (GRN) within the spectrum of clinical and pathological phenotypes of frontotemporal dementia.
    van Swieten JC, Heutink P.
    Lancet Neurol; 2008 Oct 29; 7(10):965-74. PubMed ID: 18771956
    [Abstract] [Full Text] [Related]

  • 5. Histopathological changes underlying frontotemporal lobar degeneration with clinicopathological correlation.
    Shi J, Shaw CL, Du Plessis D, Richardson AM, Bailey KL, Julien C, Stopford C, Thompson J, Varma A, Craufurd D, Tian J, Pickering-Brown S, Neary D, Snowden JS, Mann DM.
    Acta Neuropathol; 2005 Nov 29; 110(5):501-12. PubMed ID: 16222525
    [Abstract] [Full Text] [Related]

  • 6. Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study.
    Le Ber I, Camuzat A, Hannequin D, Pasquier F, Guedj E, Rovelet-Lecrux A, Hahn-Barma V, van der Zee J, Clot F, Bakchine S, Puel M, Ghanim M, Lacomblez L, Mikol J, Deramecourt V, Lejeune P, de la Sayette V, Belliard S, Vercelletto M, Meyrignac C, Van Broeckhoven C, Lambert JC, Verpillat P, Campion D, Habert MO, Dubois B, Brice A, French research network on FTD/FTD-MND.
    Brain; 2008 Mar 29; 131(Pt 3):732-46. PubMed ID: 18245784
    [Abstract] [Full Text] [Related]

  • 7. Frontotemporal dementia in The Netherlands: patient characteristics and prevalence estimates from a population-based study.
    Rosso SM, Donker Kaat L, Baks T, Joosse M, de Koning I, Pijnenburg Y, de Jong D, Dooijes D, Kamphorst W, Ravid R, Niermeijer MF, Verheij F, Kremer HP, Scheltens P, van Duijn CM, Heutink P, van Swieten JC.
    Brain; 2003 Sep 29; 126(Pt 9):2016-22. PubMed ID: 12876142
    [Abstract] [Full Text] [Related]

  • 8. Progranulin Leu271LeufsX10 is one of the most common FTLD and CBS associated mutations worldwide.
    Benussi L, Ghidoni R, Pegoiani E, Moretti DV, Zanetti O, Binetti G.
    Neurobiol Dis; 2009 Mar 29; 33(3):379-85. PubMed ID: 19101631
    [Abstract] [Full Text] [Related]

  • 9. 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 Mar 29; 7(10):1064-74. PubMed ID: 12476321
    [Abstract] [Full Text] [Related]

  • 10. [Frontotemporal lobar degeneration: a descriptive study of 42 patients].
    Reñé R, Campdelacreu J, Escrig A, Gascón-Bayarri J, Hernández-Pardo M, Jaumà S, Rubio F.
    Neurologia; 2008 Oct 29; 23(8):511-7. PubMed ID: 18802798
    [Abstract] [Full Text] [Related]

  • 11. The genetics of frontotemporal dementia.
    Haugarvoll K, Wszolek ZK, Hutton M.
    Neurol Clin; 2007 Aug 29; 25(3):697-715, vi. PubMed ID: 17659186
    [Abstract] [Full Text] [Related]

  • 12. TDP-43 pathology in familial frontotemporal dementia and motor neuron disease without Progranulin mutations.
    Seelaar H, Schelhaas HJ, Azmani A, Küsters B, Rosso S, Majoor-Krakauer D, de Rijk MC, Rizzu P, ten Brummelhuis M, van Doorn PA, Kamphorst W, Willemsen R, van Swieten JC.
    Brain; 2007 May 29; 130(Pt 5):1375-85. PubMed ID: 17360763
    [Abstract] [Full Text] [Related]

  • 13. Phenotypic heterogeneity of the GRN Asp22fs mutation in a large Italian kindred.
    Pietroboni AM, Fumagalli GG, Ghezzi L, Fenoglio C, Cortini F, Serpente M, Cantoni C, Rotondo E, Corti P, Carecchio M, Bassi M, Bresolin N, Galbiati D, Galimberti D, Scarpini E.
    J Alzheimers Dis; 2011 May 29; 24(2):253-9. PubMed ID: 21258152
    [Abstract] [Full Text] [Related]

  • 14. 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
    [Abstract] [Full Text] [Related]

  • 15. Sporadic and familial dementia with ubiquitin-positive tau-negative inclusions: clinical features of one histopathological abnormality underlying frontotemporal lobar degeneration.
    Godbolt AK, Josephs KA, Revesz T, Warrington EK, Lantos P, King A, Fox NC, Al Sarraj S, Holton J, Cipolotti L, Khan MN, Rossor MN.
    Arch Neurol; 2005 Jul 24; 62(7):1097-101. PubMed ID: 16009765
    [Abstract] [Full Text] [Related]

  • 16. Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease.
    Le Ber I, Camuzat A, Berger E, Hannequin D, Laquerrière A, Golfier V, Seilhean D, Viennet G, Couratier P, Verpillat P, Heath S, Camu W, Martinaud O, Lacomblez L, Vercelletto M, Salachas F, Sellal F, Didic M, Thomas-Anterion C, Puel M, Michel BF, Besse C, Duyckaerts C, Meininger V, Campion D, Dubois B, Brice A, French Research Network on FTD/FTD-MND.
    Neurology; 2009 May 12; 72(19):1669-76. PubMed ID: 19433740
    [Abstract] [Full Text] [Related]

  • 17. Total tau and phosphorylated tau 181 levels in the cerebrospinal fluid of patients with frontotemporal dementia due to P301L and G272V tau mutations.
    Rosso SM, van Herpen E, Pijnenburg YA, Schoonenboom NS, Scheltens P, Heutink P, van Swieten JC.
    Arch Neurol; 2003 Sep 12; 60(9):1209-13. PubMed ID: 12975285
    [Abstract] [Full Text] [Related]

  • 18. The heritability and genetics of frontotemporal lobar degeneration.
    Rohrer JD, Guerreiro R, Vandrovcova J, Uphill J, Reiman D, Beck J, Isaacs AM, Authier A, Ferrari R, Fox NC, Mackenzie IR, Warren JD, de Silva R, Holton J, Revesz T, Hardy J, Mead S, Rossor MN.
    Neurology; 2009 Nov 03; 73(18):1451-6. PubMed ID: 19884572
    [Abstract] [Full Text] [Related]

  • 19. Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohort.
    Van Langenhove T, van der Zee J, Gijselinck I, Engelborghs S, Vandenberghe R, Vandenbulcke M, De Bleecker J, Sieben A, Versijpt J, Ivanoiu A, Deryck O, Willems C, Dillen L, Philtjens S, Maes G, Bäumer V, Van Den Broeck M, Mattheijssens M, Peeters K, Martin JJ, Michotte A, Santens P, De Jonghe P, Cras P, De Deyn PP, Cruts M, Van Broeckhoven C.
    JAMA Neurol; 2013 Mar 01; 70(3):365-73. PubMed ID: 23338682
    [Abstract] [Full Text] [Related]

  • 20. 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 01; 103(6):599-606. PubMed ID: 12012092
    [Abstract] [Full Text] [Related]

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