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Journal Abstract Search

134 related items for PubMed ID: 31740511

  • 1. Clinical Reasoning: Progressive proximal weakness in a 56-year-old man with bone pain.
    Torabi T, Huttner A, Nowak RJ, Roy B.
    Neurology; 2019 Nov 19; 93(21):939-944. PubMed ID: 31740511
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  • 3. The multifaceted clinical presentation of VCP-proteinopathy in a Greek family.
    Papadimas GK, Paraskevas GP, Zambelis T, Karagiaouris C, Bourbouli M, Bougea A, Walter MC, Schumacher NU, Krause S, Kapaki E.
    Acta Myol; 2017 Dec 19; 36(4):203-206. PubMed ID: 29770363
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  • 4. Phenotypic variability in three families with valosin-containing protein mutation.
    Spina S, Van Laar AD, Murrell JR, Hamilton RL, Kofler JK, Epperson F, Farlow MR, Lopez OL, Quinlan J, DeKosky ST, Ghetti B.
    Eur J Neurol; 2013 Feb 19; 20(2):251-8. PubMed ID: 22900631
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  • 6. A cross-sectional analysis of clinical evaluation in 35 individuals with mutations of the valosin-containing protein gene.
    Plewa J, Surampalli A, Wencel M, Milad M, Donkervoort S, Caiozzo VJ, Goyal N, Mozaffar T, Kimonis V.
    Neuromuscul Disord; 2018 Sep 19; 28(9):778-786. PubMed ID: 30097247
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  • 8. The heterozygous R155C VCP mutation: Toxic in humans! Harmless in mice?
    Clemen CS, Winter L, Strucksberg KH, Berwanger C, Türk M, Kornblum C, Florin A, Aguilar-Pimentel JA, Amarie OV, Becker L, Garrett L, Hans W, Moreth K, Neff F, Pingen L, Rathkolb B, Rácz I, Rozman J, Treise I, Fuchs H, Gailus-Durner V, de Angelis MH, Vorgerd M, Eichinger L, Schröder R.
    Biochem Biophys Res Commun; 2018 Sep 18; 503(4):2770-2777. PubMed ID: 30100055
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  • 9. Muscle wasting, bone pain and cognitive decline: a unifying diagnosis.
    St John L, Larner AJ.
    Br J Hosp Med (Lond); 2015 Oct 18; 76(10):602-3. PubMed ID: 26457944
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  • 11. Motor neuron involvement in multisystem proteinopathy: implications for ALS.
    Benatar M, Wuu J, Fernandez C, Weihl CC, Katzen H, Steele J, Oskarsson B, Taylor JP.
    Neurology; 2013 May 14; 80(20):1874-80. PubMed ID: 23635965
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  • 13. 215th ENMC International Workshop VCP-related multi-system proteinopathy (IBMPFD) 13-15 November 2015, Heemskerk, The Netherlands.
    Evangelista T, Weihl CC, Kimonis V, Lochmüller H, VCP related diseases Consortium.
    Neuromuscul Disord; 2016 Aug 14; 26(8):535-47. PubMed ID: 27312024
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  • 14. Nuclear inclusions mimicking poly(A)-binding protein nuclear 1 inclusions in a case of inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia with a novel mutation in the valosin-containing protein gene.
    Matsubara S, Shimizu T, Komori T, Mori-Yoshimura M, Minami N, Hayashi YK.
    Neuromuscul Disord; 2016 Jul 14; 26(7):436-40. PubMed ID: 27209344
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  • 15. The Myoblast C2C12 Transfected with Mutant Valosin-Containing Protein Exhibits Delayed Stress Granule Resolution on Oxidative Stress.
    Rodriguez-Ortiz CJ, Flores JC, Valenzuela JA, Rodriguez GJ, Zumkehr J, Tran DN, Kimonis VE, Kitazawa M.
    Am J Pathol; 2016 Jun 14; 186(6):1623-34. PubMed ID: 27106764
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  • 17. [A case of inclusion body myopathy with Paget's disease of bone and frontotemporal dementia (IBMPFD) showing clinical features of motor neuron disease].
    Igari R, Wada M, Sato H, K Hayashi Y, Nishino I, Kato T.
    Rinsho Shinkeigaku; 2013 Jun 14; 53(6):458-64. PubMed ID: 23782824
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  • 18. A Brazilian family with inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia linked to the VCP pGly97Glu mutation.
    Shinjo SK, Oba-Shinjo SM, Lerario AM, Marie SKN.
    Clin Rheumatol; 2018 Apr 14; 37(4):1129-1136. PubMed ID: 29127544
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  • 19. [An advanced case of myopathy and dementia with a new mutation in the valosin-containing protein gene].
    Kamiyama T, Sengoku R, Sasaki M, Hayashi Y, Nishino I, Mochio S, Iguchi Y.
    Rinsho Shinkeigaku; 2013 Apr 14; 53(6):465-9. PubMed ID: 23782825
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