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Journal Abstract Search

246 related items for PubMed ID: 18328591

  • 1. Loss of progranulin function in frontotemporal lobar degeneration.
    Cruts M, Van Broeckhoven C.
    Trends Genet; 2008 Apr; 24(4):186-94. PubMed ID: 18328591
    [Abstract] [Full Text] [Related]

  • 2. Granulin mutations associated with frontotemporal lobar degeneration and related disorders: an update.
    Gijselinck I, Van Broeckhoven C, Cruts M.
    Hum Mutat; 2008 Dec; 29(12):1373-86. PubMed ID: 18543312
    [Abstract] [Full Text] [Related]

  • 3. 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; 33(3):379-85. PubMed ID: 19101631
    [Abstract] [Full Text] [Related]

  • 4. Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease.
    Brouwers N, Sleegers K, Engelborghs S, Maurer-Stroh S, Gijselinck I, van der Zee J, Pickut BA, Van den Broeck M, Mattheijssens M, Peeters K, Schymkowitz J, Rousseau F, Martin JJ, Cruts M, De Deyn PP, Van Broeckhoven C.
    Neurology; 2008 Aug 26; 71(9):656-64. PubMed ID: 18565828
    [Abstract] [Full Text] [Related]

  • 5. Low plasma progranulin levels predict progranulin mutations in frontotemporal lobar degeneration.
    Ghidoni R, Benussi L, Glionna M, Franzoni M, Binetti G.
    Neurology; 2008 Oct 14; 71(16):1235-9. PubMed ID: 18768919
    [Abstract] [Full Text] [Related]

  • 6. Serum biomarker for progranulin-associated frontotemporal lobar degeneration.
    Sleegers K, Brouwers N, Van Damme P, Engelborghs S, Gijselinck I, van der Zee J, Peeters K, Mattheijssens M, Cruts M, Vandenberghe R, De Deyn PP, Robberecht W, Van Broeckhoven C.
    Ann Neurol; 2009 May 14; 65(5):603-9. PubMed ID: 19288468
    [Abstract] [Full Text] [Related]

  • 7. 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
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  • 9. 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 14; 31(1):41-5. PubMed ID: 18479928
    [Abstract] [Full Text] [Related]

  • 10. 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 14; 15(3):369-74. PubMed ID: 17228326
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  • 12. 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 14; 66(2):142-51. PubMed ID: 17278999
    [Abstract] [Full Text] [Related]

  • 13. Progranulin variability has no major role in Parkinson disease genetic etiology.
    Nuytemans K, Pals P, Sleegers K, Engelborghs S, Corsmit E, Peeters K, Pickut B, Mattheijssens M, Cras P, De Deyn PP, Theuns J, Van Broeckhoven C.
    Neurology; 2008 Oct 07; 71(15):1147-51. PubMed ID: 18838661
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  • 15. Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family.
    Brouwers N, Nuytemans K, van der Zee J, Gijselinck I, Engelborghs S, Theuns J, Kumar-Singh S, Pickut BA, Pals P, Dermaut B, Bogaerts V, De Pooter T, Serneels S, Van den Broeck M, Cuijt I, Mattheijssens M, Peeters K, Sciot R, Martin JJ, Cras P, Santens P, Vandenberghe R, De Deyn PP, Cruts M, Van Broeckhoven C, Sleegers K.
    Arch Neurol; 2007 Oct 07; 64(10):1436-46. PubMed ID: 17923627
    [Abstract] [Full Text] [Related]

  • 16. 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 Oct 07; 21(1):1-7. PubMed ID: 17334266
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  • 18. 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]

  • 19. "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
    [Abstract] [Full Text] [Related]

  • 20. Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations.
    Pickering-Brown SM, Rollinson S, Du Plessis D, Morrison KE, Varma A, Richardson AM, Neary D, Snowden JS, Mann DM.
    Brain; 2008 Mar 27; 131(Pt 3):721-31. PubMed ID: 18192287
    [Abstract] [Full Text] [Related]

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