Heterogeneity in Familial Dominant Paget Disease of Bone and Muscular Dystrophy

Clinical Delineation and Localization to Chromosome 9p13.3–p12 of a Unique Dominant Disorder in Four Families: Hereditary Inclusion Body Myopathy, Paget Disease of Bone, and Frontotemporal Dementia

Clinical and molecular studies in a unique family with autosomal dominant limb-girdle muscular dystrophy and Paget disease of bone

Autosomal Dominant Inclusion Body Myopathy, Paget Disease of Bone, and Frontotemporal Dementia

Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused

Clinical and genetic heterogeneity in chromosome 9p associated hereditary inclusion body myopathy

Mapping autosomal dominant progressive limb-girdle myopathy with bone fragility to chromosome 9p21-p22

Novel ubiquitin neuropathology in frontotemporal dementia with

Pathological consequences of VCP mutations on human striated muscle

APOE is a Potential Modifier Gene in an Autosomal Dominant Form of Frontotemporal Dementia (IBMPFD)

TDP-43 in the Ubiquitin Pathology of Frontotemporal Dementia with VCP gene mutations

Novel VCP Mutations in Inclusion Body Myopathy associated with Paget Disease of Bone and Frontotemporal

Nuclear localization of valosin-containing protein in normal muscle

TDP43 accumulation in inclusion body myopathy

VCP Disease associated with myopathy, Paget Disease of Bone and Frontotemporal Dementia

 Valosin-containing protein disease Inclusion body myopathy with Paget’s disease of the bone

 Valosin containing protein associated inclusion body myopathy abnormal vacuolization autophagy and cell fusion in myo

 VCP p97 is essential for maturation of ubiquitin-containing autophagosomes

 VCP Associated Inclusion Body Myopathy and Paget Disease of Bone Knock-In Mouse

A Brazilian family with hereditary inclusion body myopathy associated with Paget disease of bone

 Radiological Features of Paget Disease of Bone Associated with VCP Inclusion Body Myopathy

  Valosin-containing protein mutation and Parkinson disease

  Inclusion Body Myopathy with Paget Disease of Bone and or Frontotemporal Dementia

  The Multiple Faces of Valosin-95 Containing Protein-Associated Diseases Inclusion Body

  Global gene profiling of VCP-associated inclusion body

  Genotype-Phenotype studies of VCP-associated Inclusion Body

 Clinical and radiological features in young individuals with nevoid basal cell carcinoma syndrome

 The Homozygote VCPR155H-R155H Mouse Model Exhibits Accelerated Human VCP Associated Disease Pathology

 Cytokine Profiling in Patients with VCP-Associated Disease

 Exercise Training Reverses Skeletal Muscle Atrophy in an Experimental Model of VCP Disease

 Lipid-enriched diet rescues lethality and slows down progression in a murine model of VCP-associated disease

 Disease-specific induced pluripotent stem cell modeling insights into the pathophysiology of VCP disease

 The Influence of Diet and Exercise on the Physical Health of Affected Individuals with VCP Disease

 Psychological Impact of Predictive Genetic Testing in VCP Inclusion Body Myopathy, Paget Disease

 Global Gene Expression Profiling in R155H Knock-In Murine Model of VCP Disease

Targeted Excision of VCP R155H Mutation cy Cre-LOxP Technology as Promoting Theraputic Strategy for VCP Disease

Rapamycin and Chloroquine The In Vitro abd In Vitro Effects of Autophagy Modifying Drugs Show Promising Results in VCP M

 In vitro studies in VCP-associated multisystem proteinopathy suggest altered mitochondrial bioenergetic

 A Fine Balance of Dietary Lipids Improves Pathology of a Murine Modelof VCPAssociated Multimodel Proteinopathy

 Myoblast C2C12

  VCP-related multi-system proteinopathy 215th ENMC International Workshop

  Activation of the NLRP3 Inflammasome Is Associated with Valosin-Containing Protein Myopathy

  Valosin-containing protein (VCP) Disease and Familial Alzheimer’s Disease

  Clinical spectrum of VCP myopathy FINAL

  VCP Disease

  Myogenic differentiation of VCP disease-induced pluripotent stem cells

  Genotype-phenotype study in VCP disease

  Novel Valosin-Containing Protein Mutations Associated With Multisystem Proteinopathy

 Genotype–phenotype studies of VCP-associated inclusion body myopathy with Paget disease of bone and/or frontotemporal dementia