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Journal Abstract Search

165 related items for PubMed ID: 30029282

  • 1.
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  • 2. 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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  • 3. 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; 37(4):1129-1136. PubMed ID: 29127544
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  • 7. [Inclusion body myopathy with Paget's disease of bone and frontotemporal dementia].
    Hayashi Y.
    Rinsho Shinkeigaku; 2013 Apr; 53(11):947-50. PubMed ID: 24291843
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  • 8. 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; 20(2):251-8. PubMed ID: 22900631
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  • 11. [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 Feb; 53(6):465-9. PubMed ID: 23782825
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  • 13. Bone scan findings of Paget's disease of bone in patients with VCP Multisystem Proteinopathy 1.
    Columbres RCA, Din S, Gibbs L, Kimonis V.
    Sci Rep; 2024 Mar 11; 14(1):5917. PubMed ID: 38467645
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  • 14. 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 11; 169():105722. PubMed ID: 35405261
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  • 15. 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 11; 26(7):436-40. PubMed ID: 27209344
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  • 17. Ubiquitin- and ATP-dependent unfoldase activity of P97/VCP•NPLOC4•UFD1L is enhanced by a mutation that causes multisystem proteinopathy.
    Blythe EE, Olson KC, Chau V, Deshaies RJ.
    Proc Natl Acad Sci U S A; 2017 May 30; 114(22):E4380-E4388. PubMed ID: 28512218
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  • 18. Novel valosin containing protein mutation in a Swiss family with hereditary inclusion body myopathy and dementia.
    Peyer AK, Kinter J, Hench J, Frank S, Fuhr P, Thomann S, Fischmann A, Kneifel S, Camaño P, López de Munain A, Sinnreich M, Renaud S.
    Neuromuscul Disord; 2013 Feb 30; 23(2):149-54. PubMed ID: 23140793
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  • 19. 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 30; 52(1):9-16. PubMed ID: 23000505
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