| P50 | author | Yannick Béjot | Q42746457 |
| P2093 | author name string | Maurice Giroud | |
| | Olivier Rouaud | |
| | Thibault Moreau | |
| | Marie Sarazin | |
| | Tania Stojkovic | |
| | Agnès Jacquin | |
| | Inna Dygai-Cochet | |
| | Pierre Soichot | |
| | Martine Lemesle-Martin | |
| P2860 | cites work | Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein | Q29619232 |
| | VCP disease associated with myopathy, Paget disease of bone and frontotemporal dementia: review of a unique disorder | Q34849448 |
| | Valosin-containing protein disease: inclusion body myopathy with Paget's disease of the bone and fronto-temporal dementia | Q37452177 |
| | Structural brain imaging in frontotemporal dementia. | Q37917017 |
| | TDP-43 accumulation in inclusion body myopathy muscle suggests a common pathogenic mechanism with frontotemporal dementia | Q41667459 |
| | Two Australian families with inclusion-body myopathy, Paget's disease of bone and frontotemporal dementia: novel clinical and genetic findings | Q43119772 |
| | Mutant valosin-containing protein causes a novel type of frontotemporal dementia | Q45283163 |
| | A novel mutation in the VCP gene (G157R) in a German family with inclusion-body myopathy with Paget disease of bone and frontotemporal dementia | Q46126082 |
| | Clinical outcome in 19 French and Spanish patients with valosin-containing protein myopathy associated with Paget's disease of bone and frontotemporal dementia | Q48012937 |
| | Valosin-containing protein gene mutations: clinical and neuropathologic features | Q48491139 |
| | Direct voxel-based comparison between grey matter hypometabolism and atrophy in Alzheimer's disease. | Q53390356 |
| | 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. | Q53492125 |
| | An Italian family with inclusion-body myopathy and frontotemporal dementia due to mutation in the VCP gene. | Q53531100 |
| | Inclusion body myopathy and Paget disease is linked to a novel mutation in the VCP gene | Q58050234 |
| | Inclusion body myopathy and frontotemporal dementia caused by a novel VCP mutation | Q59543699 |
| P433 | issue | 3 | |
| P921 | main subject | frontotemporal dementia | Q18592 |
| P304 | page(s) | 187-194 | |
| P577 | publication date | 2013-10-31 | |
| P1433 | published in | Case reports in neurology | Q27722665 |
| P1476 | title | Psychiatric Presentation of Frontotemporal Dementia Associated with Inclusion Body Myopathy due to the VCP Mutation (R155H) in a French Family | |
| P478 | volume | 5 | |