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Journal Abstract Search

340 related items for PubMed ID: 17457594

  • 1. 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; 114(1):55-61. PubMed ID: 17457594
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  • 2. Inclusion body myopathy-associated mutations in p97/VCP impair endoplasmic reticulum-associated degradation.
    Weihl CC, Dalal S, Pestronk A, Hanson PI.
    Hum Mol Genet; 2006 Jan 15; 15(2):189-99. PubMed ID: 16321991
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  • 3. Valosin-containing protein gene mutations: clinical and neuropathologic features.
    Guyant-Maréchal L, Laquerrière A, Duyckaerts C, Dumanchin C, Bou J, Dugny F, Le Ber I, Frébourg T, Hannequin D, Campion D.
    Neurology; 2006 Aug 22; 67(4):644-51. PubMed ID: 16790606
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  • 4. A novel mutation in the VCP gene (G157R) in a German family with inclusion-body myopathy with Paget disease of bone and frontotemporal dementia.
    Djamshidian A, Schaefer J, Haubenberger D, Stogmann E, Zimprich F, Auff E, Zimprich A.
    Muscle Nerve; 2009 Mar 22; 39(3):389-91. PubMed ID: 19208399
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  • 5. TDP-43 in the ubiquitin pathology of frontotemporal dementia with VCP gene mutations.
    Neumann M, Mackenzie IR, Cairns NJ, Boyer PJ, Markesbery WR, Smith CD, Taylor JP, Kretzschmar HA, Kimonis VE, Forman MS.
    J Neuropathol Exp Neurol; 2007 Feb 22; 66(2):152-7. PubMed ID: 17279000
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  • 6. An Italian family with inclusion-body myopathy and frontotemporal dementia due to mutation in the VCP gene.
    Gidaro T, Modoni A, Sabatelli M, Tasca G, Broccolini A, Mirabella M.
    Muscle Nerve; 2008 Jan 22; 37(1):111-4. PubMed ID: 17763460
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  • 7. Pathological consequences of VCP mutations on human striated muscle.
    Hübbers CU, Clemen CS, Kesper K, Böddrich A, Hofmann A, Kämäräinen O, Tolksdorf K, Stumpf M, Reichelt J, Roth U, Krause S, Watts G, Kimonis V, Wattjes MP, Reimann J, Thal DR, Biermann K, Evert BO, Lochmüller H, Wanker EE, Schoser BG, Noegel AA, Schröder R.
    Brain; 2007 Feb 22; 130(Pt 2):381-93. PubMed ID: 16984901
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  • 9. Clinical heterogeneity in 3 unrelated families linked to VCP p.Arg159His.
    van der Zee J, Pirici D, Van Langenhove T, Engelborghs S, Vandenberghe R, Hoffmann M, Pusswald G, Van den Broeck M, Peeters K, Mattheijssens M, Martin JJ, De Deyn PP, Cruts M, Haubenberger D, Kumar-Singh S, Zimprich A, Van Broeckhoven C.
    Neurology; 2009 Aug 25; 73(8):626-32. PubMed ID: 19704082
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  • 10. Enhanced ATPase activities as a primary defect of mutant valosin-containing proteins that cause inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia.
    Manno A, Noguchi M, Fukushi J, Motohashi Y, Kakizuka A.
    Genes Cells; 2010 Aug 25; 15(8):911-22. PubMed ID: 20604808
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  • 18. The multiple faces of valosin-containing protein-associated diseases: inclusion body myopathy with Paget's disease of bone, frontotemporal dementia, and amyotrophic lateral sclerosis.
    Nalbandian A, Donkervoort S, Dec E, Badadani M, Katheria V, Rana P, Nguyen C, Mukherjee J, Caiozzo V, Martin B, Watts GD, Vesa J, Smith C, Kimonis VE.
    J Mol Neurosci; 2011 Nov 25; 45(3):522-31. PubMed ID: 21892620
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