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Journal Abstract Search

110 related items for PubMed ID: 17417739

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  • 6. Mutations in progranulin gene: clinical, pathological, and ribonucleic acid expression findings.
    López de Munain A, Alzualde A, Gorostidi A, Otaegui D, Ruiz-Martínez J, Indakoetxea B, Ferrer I, Pérez-Tur J, Sáenz A, Bergareche A, Barandiarán M, Poza JJ, Zabalza R, Ruiz I, Urtasun M, Fernández-Manchola I, Olasagasti B, Espinal JB, Olaskoaga J, Ruibal M, Moreno F, Carrera N, Martí Massó JF.
    Biol Psychiatry; 2008 May 15; 63(10):946-52. PubMed ID: 17950702
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  • 7. 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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  • 10. Dissecting the complexity of frontotemporal dementia: genotypes, phenotypes, and phenocopies.
    Klein C, Bonifati V.
    Neurology; 2007 Jul 10; 69(2):129-30. PubMed ID: 17620543
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  • 11. Frontotemporal dementia and parkinsonism associated with the IVS1+1G->A mutation in progranulin: a clinicopathologic study.
    Boeve BF, Baker M, Dickson DW, Parisi JE, Giannini C, Josephs KA, Hutton M, Pickering-Brown SM, Rademakers R, Tang-Wai D, Jack CR, Kantarci K, Shiung MM, Golde T, Smith GE, Geda YE, Knopman DS, Petersen RC.
    Brain; 2006 Nov 10; 129(Pt 11):3103-14. PubMed ID: 17030535
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  • 14. 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 10; 15(3):369-74. PubMed ID: 17228326
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  • 15. Clinicopathologic features of frontotemporal dementia with progranulin sequence variation.
    Spina S, Murrell JR, Huey ED, Wassermann EM, Pietrini P, Baraibar MA, Barbeito AG, Troncoso JC, Vidal R, Ghetti B, Grafman J.
    Neurology; 2007 Mar 13; 68(11):820-7. PubMed ID: 17202431
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  • 16. 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 13; 110(5):501-12. PubMed ID: 16222525
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  • 18. Progranulin mutation analysis: Identification of one novel mutation in exon 12 associated with frontotemporal dementia.
    Aswathy PM, Jairani PS, Raghavan SK, Verghese J, Gopala S, Srinivas P, Mathuranath PS.
    Neurobiol Aging; 2016 Mar 13; 39():218.e1-3. PubMed ID: 26724960
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  • 19. Clinical, genetic, and pathologic characteristics of patients with frontotemporal dementia and progranulin mutations.
    Van Deerlin VM, Wood EM, Moore P, Yuan W, Forman MS, Clark CM, Neumann M, Kwong LK, Trojanowski JQ, Lee VM, Grossman M.
    Arch Neurol; 2007 Aug 13; 64(8):1148-53. PubMed ID: 17698705
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  • 20. Progranulin genetic variability contributes to amyotrophic lateral sclerosis.
    Sleegers K, Brouwers N, Maurer-Stroh S, van Es MA, Van Damme P, van Vught PW, van der Zee J, Serneels S, De Pooter T, Van den Broeck M, Cruts M, Schymkowitz J, De Jonghe P, Rousseau F, van den Berg LH, Robberecht W, Van Broeckhoven C.
    Neurology; 2008 Jul 22; 71(4):253-9. PubMed ID: 18184915
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