Disease: Inclusion body myopathy- autosomal dominant
- A clinicopathologic study of malignancy in VCP-associated multisystem proteinopathy
- A novel autosomal dominant inclusion body myopathy linked to 7q22.1-31.1
- A Novel Mutation (D395A) in Valosin-Containing Protein Gene Is Associated With Early Onset Frontotemporal Dementia in an Italian Family
- Another VCP interactor: NF is enough
- Autophagic vacuolar myopathy involving the phenotype of spinocerebellar ataxia type 3
- C-terminal frameshift variant of TDP-43 with pronounced aggregation-propensity causes rimmed vacuole myopathy but not ALS/FTD
- Characteristics of VCP mutation-associated cardiomyopathy
- Expression of the inclusion body myopathy 3 mutation in Drosophila depresses myosin function and stability and recapitulates muscle inclusions and weakness
- From neurodevelopment to neurodegeneration: the interaction of neurofibromin and valosin-containing protein/p97 in regulation of dendritic spine formation
- Genetic interaction of hnRNPA2B1 and DNAJB6 in a Drosophila model of multisystem proteinopathy
- Hereditary inclusion-body myopathies
- Inclusion Body Myopathy with Paget Disease of Bone and/or Frontotemporal Dementia
- Multisystem Proteinopathy Due to <em>VCP</em> Mutations: A Review of Clinical Heterogeneity and Genetic Diagnosis
- Myofibrillar myopathies due to a novel mutation in exon 8 of the LDB3 gene
- Myopathies with finger flexor weakness: Not only inclusion-body myositis
- Novel Variants in the <em>VCP</em> Gene Causing Multisystem Proteinopathy 1
- Positron emission tomography and magnetic resonance imaging methods and datasets within the Dominantly Inherited Alzheimer Network (DIAN)
- Prevalence of Frontotemporal Dementia in Females of 5 Hispanic Families With R159H VCP Multisystem Proteinopathy
- Remote respiratory resistance exercise training improves respiratory function in individuals with VCP multisystem proteinopathy
- Severe cardiomyopathy associated with the VCP p.R155C and c.177_187del MYBPC3 gene variants
- Sex influences clinical phenotype in valosin-containing protein mutations: A case family report and systematic literature review
- Skeletal muscle cell protein dysregulation highlights the pathogenesis mechanism of myopathy-associated p97/VCP R155H mutations
- Update on the pathogenesis and genetics of Paget's disease of bone
- Valosin-containing protein and neurofibromin interact to regulate dendritic spine density