Psychiatric presentation of frontotemporal dementia associated with inclusion body myopathy due to the VCP mutation (R155H) in a French family

Case Reports in Neurology

Volumn 5, Issue 3, 2013, Pages 187-194

  Jacquin, Agnès ^a   Rouaud, Olivier ^a   Soichot, Pierre ^a   Bejot, Yannick ^a   Dygai Cochet, Inna ^b   Sarazin, Marie ^c   Stojkovic, Tania ^d   Lemesle Martin, Martine ^a   Giroud, Maurice ^a   Moreau, Thibault ^a  

^a DIJON UNIVERSITY HOSPITAL   (France)

^b CENTRE GEORGES FRANÇOIS LECLERC   (France)

^c Pavillon Jean Lhermitte   (France)

^d PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

Author keywords

Frontotemporal dementia; Inclusion body myopathy; Psychiatric disorders; VCP mutation

Indexed keywords

VALOSIN CONTAINING PROTEIN;

ADULT; ANXIETY; APHASIA; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BASAL GANGLION; BEHAVIOR CHANGE; BRAIN DYSFUNCTION; CASE REPORT; COGNITIVE DEFECT; DISEASE SEVERITY; ELECTROMYOGRAPHY; EXECUTIVE FUNCTION; FAMILY; FRONTAL LOBE; GENE MUTATION; GENETIC ANALYSIS; HISTOPATHOLOGY; HOSPITALIZATION; HUMAN; INCLUSION BODY MYOPATHY WITH PAGET DISEASE OF THE BONE AND FRONTOTEMPORAL DEMENT; IRRITABILITY; LIMB WEAKNESS; MAJOR DEPRESSION; MALE; MENTAL DISEASE; MENTAL HOSPITAL; MINI MENTAL STATE EXAMINATION; MUSCLE ATROPHY; MUSCLE BIOPSY; NUCLEAR MAGNETIC RESONANCE IMAGING; POSITRON EMISSION TOMOGRAPHY; PRIORITY JOURNAL; RARE DISEASE; TEMPORAL LOBE; WHEELCHAIR;

EID: 84892981725     PISSN: 1662680X     EISSN: None     Source Type: Journal    
DOI: 10.1159/000356481     Document Type: Article

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