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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

546 related items for PubMed ID: 18184915

  • 1.
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  • 2. 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
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  • 3. 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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  • 4. 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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  • 5. Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementia.
    van der Zee J, Le Ber I, Maurer-Stroh S, Engelborghs S, Gijselinck I, Camuzat A, Brouwers N, Vandenberghe R, Sleegers K, Hannequin D, Dermaut B, Schymkowitz J, Campion D, Santens P, Martin JJ, Lacomblez L, De Pooter T, Peeters K, Mattheijssens M, Vercelletto M, Van den Broeck M, Cruts M, De Deyn PP, Rousseau F, Brice A, Van Broeckhoven C.
    Hum Mutat; 2007 Apr 24; 28(4):416. PubMed ID: 17345602
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  • 6. 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 24; 64(10):1436-46. PubMed ID: 17923627
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  • 7. 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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  • 10. 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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  • 11. Lack of association between VEGF polymorphisms and ALS in a Dutch population.
    Van Vught PW, Sutedja NA, Veldink JH, Koeleman BP, Groeneveld GJ, Wijmenga C, Uitdehaag BM, de Jong JM, Baas F, Wokke JH, Van den Berg LH.
    Neurology; 2005 Nov 22; 65(10):1643-5. PubMed ID: 16301496
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  • 12. Association of the hOGG1 Ser326Cys polymorphism with sporadic amyotrophic lateral sclerosis.
    Coppedè F, Mancuso M, Lo Gerfo A, Carlesi C, Piazza S, Rocchi A, Petrozzi L, Nesti C, Micheli D, Bacci A, Migliore L, Murri L, Siciliano G.
    Neurosci Lett; 2007 Jun 13; 420(2):163-8. PubMed ID: 17531381
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  • 13. Is erythropoietin gene a modifier factor in amyotrophic lateral sclerosis?
    Ghezzi S, Del Bo R, Scarlato M, Nardini M, Carlesi C, Prelle A, Corti S, Mancuso M, Briani C, Siciliano G, Murri L, Bresolin N, Comi GP.
    Neurobiol Aging; 2009 May 13; 30(5):842-4. PubMed ID: 17888545
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  • 14. Progranulin locus deletion in frontotemporal dementia.
    Gijselinck I, van der Zee J, Engelborghs S, Goossens D, Peeters K, Mattheijssens M, Corsmit E, Del-Favero J, De Deyn PP, Van Broeckhoven C, Cruts M.
    Hum Mutat; 2008 Jan 13; 29(1):53-8. PubMed ID: 18157829
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  • 15. A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia.
    Morita M, Al-Chalabi A, Andersen PM, Hosler B, Sapp P, Englund E, Mitchell JE, Habgood JJ, de Belleroche J, Xi J, Jongjaroenprasert W, Horvitz HR, Gunnarsson LG, Brown RH.
    Neurology; 2006 Mar 28; 66(6):839-44. PubMed ID: 16421333
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  • 18. 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
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  • 20. Rare and common paraoxonase gene variants in amyotrophic lateral sclerosis patients.
    van Blitterswijk M, Blokhuis A, van Es MA, van Vught PW, Rowicka PA, Schelhaas HJ, van der Kooi AJ, de Visser M, Veldink JH, van den Berg LH.
    Neurobiol Aging; 2012 Aug 12; 33(8):1845.e1-3. PubMed ID: 22330174
    [Abstract] [Full Text] [Related]

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