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Journal Abstract Search

313 related items for PubMed ID: 19638255

  • 1. The molecular basis of frontotemporal dementia.
    Neumann M, Tolnay M, Mackenzie IR.
    Expert Rev Mol Med; 2009 Jul 29; 11():e23. PubMed ID: 19638255
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  • 2. 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 Jul 29; 4(2-3):227-35. PubMed ID: 17596717
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  • 8. Pathology and genetics of frontotemporal lobar degeneration: an update.
    Tolnay M, Frank S.
    Clin Neuropathol; 2007 Jul 29; 26(4):143-56. PubMed ID: 17702495
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  • 11. [The molecular pathology of frontotemporal lobar degeneration].
    Fujishiro H, Hasegawa M, Arai T.
    Seishin Shinkeigaku Zasshi; 2010 Jul 29; 112(4):313-24. PubMed ID: 20496755
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  • 14. 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
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  • 16. Valosin-containing protein and the pathogenesis of frontotemporal dementia associated with inclusion body myopathy.
    Guinto JB, Ritson GP, Taylor JP, Forman MS.
    Acta Neuropathol; 2007 Jul 29; 114(1):55-61. PubMed ID: 17457594
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