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Journal Abstract Search

166 related items for PubMed ID: 38467645

  • 1.
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  • 2. Cross-sectional study of patients with VCP multisystem proteinopathy 1 using dual-energy x-ray absorptiometry.
    Columbres RCA, Luu V, Nguyen M, Kimonis V.
    Muscle Nerve; 2024 Jun; 69(6):699-707. PubMed ID: 38551101
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  • 3. Characteristics of VCP mutation-associated cardiomyopathy.
    Wang SC, Smith CD, Lombardo DM, Kimonis V.
    Neuromuscul Disord; 2021 Aug; 31(8):701-705. PubMed ID: 34244020
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  • 4. Novel Variants in the VCP Gene Causing Multisystem Proteinopathy 1.
    Columbres RCA, Chin Y, Pratti S, Quinn C, Gonzalez-Cuyar LF, Weiss M, Quintero-Rivera F, Kimonis V.
    Genes (Basel); 2023 Mar 08; 14(3):. PubMed ID: 36980948
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  • 5. The Cure VCP Scientific Conference 2021: Molecular and clinical insights into neurodegeneration and myopathy linked to multisystem proteinopathy-1 (MSP-1).
    Johnson MA, Klickstein JA, Khanna R, Gou Y, Cure VCP Disease Research Consortium, Raman M.
    Neurobiol Dis; 2022 Jul 08; 169():105722. PubMed ID: 35405261
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  • 7. A novel VCP mutation as the cause of atypical IBMPFD in a Chinese family.
    Gu JM, Ke YH, Yue H, Liu YJ, Zhang Z, Zhang H, Hu WW, Wang C, He JW, Hu YQ, Li M, Fu WZ, Zhang ZL.
    Bone; 2013 Jan 08; 52(1):9-16. PubMed ID: 23000505
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  • 9. 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 08; 37(4):1129-1136. PubMed ID: 29127544
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  • 11. Clinical, Biochemical, Radiological, and Genetic Analyses of a Patient with VCP Gene Variant-Induced Paget's Disease of Bone.
    Zhang Y, Gao P, Yan S, Zhang Q, Wang O, Jiang Y, Xing X, Xia W, Li M.
    Calcif Tissue Int; 2022 Apr 08; 110(4):518-528. PubMed ID: 34800131
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  • 12. 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 08; 20(2):251-8. PubMed ID: 22900631
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  • 13. 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 08; 45(3):522-31. PubMed ID: 21892620
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  • 16. [Inclusion body myopathy with Paget's disease of bone and frontotemporal dementia].
    Hayashi Y.
    Rinsho Shinkeigaku; 2013 Nov 08; 53(11):947-50. PubMed ID: 24291843
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  • 17. 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 08; 36(4):203-206. PubMed ID: 29770363
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  • 18. Evaluation of the role of Valosin-containing protein in the pathogenesis of familial and sporadic Paget's disease of bone.
    Lucas GJ, Mehta SG, Hocking LJ, Stewart TL, Cundy T, Nicholson GC, Walsh JP, Fraser WD, Watts GD, Ralston SH, Kimonis VE.
    Bone; 2006 Feb 08; 38(2):280-5. PubMed ID: 16199218
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  • 19. Valosin-containing protein disease: inclusion body myopathy with Paget's disease of the bone and fronto-temporal dementia.
    Weihl CC, Pestronk A, Kimonis VE.
    Neuromuscul Disord; 2009 May 08; 19(5):308-15. PubMed ID: 19380227
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  • 20. Inclusion body myopathy, Paget's disease of the bone and frontotemporal dementia: recurrence of the VCP R155H mutation in an Italian family and implications for genetic counselling.
    Viassolo V, Previtali SC, Schiatti E, Magnani G, Minetti C, Zara F, Grasso M, Dagna-Bricarelli F, Di Maria E.
    Clin Genet; 2008 Jul 08; 74(1):54-60. PubMed ID: 18341608
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