Introduction: Mutations in the progranulin (GRN) gene are a major source of inherited frontotemporal degeneration (FTD) spectrum disorders associated with TDP-43 proteinopathy. We use structural MRI to identify regions of baseline differences and longitudinal changes in gray matter (GM) and white matter (WM) in presymptomatic GRN mutation carriers (pGRN+) compared to young controls (yCTL). Methods: Cognitively intact first-degree relatives of symptomatic GRN+ FTD patients with identified GRN mutations (pGRN+; N = 11, mean age = 41.4) and matched yCTL (N = 11, mean age = 53.6) were identified. They completed a MRI session with T1-weighted imaging to assess GM density (GMD) and diffusion-weighted imaging (DWI) to assess fractional anisotropy ...
Frontotemporal dementia (FTD) is a neurodegenerative disease with a strong genetic basis. Understand...
Several causative gene mutations have been identified in frontotemporal lobar degeneration (FTLD), i...
International audienceThe preclinical stage of frontotemporal lobar degeneration (FTLD) is not well ...
Mutations in the progranulin (PGRN) gene have been recently demonstrated as a cause of frontotempora...
International audienceMutations in the progranulin (GRN) gene are responsible for 20% of familial ca...
In genetic frontotemporal dementia, cross-sectional studies have identified profiles of presymptomat...
Loss-of-function mutations in the progranulin gene (GRN) are one of the major causes of familial fro...
Frontotemporal dementia (FTD) is a heterogeneous group of neurodegenerative disorders with both spor...
Frontotemporal dementia (FTD) is a heterogeneous group of neurodegenerative disorders with both spor...
AbstractNeural network breakdown is a key issue in neurodegenerative disease, but the mechanisms are...
White matter hyperintensities (WMH) are often seen on MRI brain scans in frontotemporal dementia (FT...
Granulin (GRN) mutations have been identified as a major cause of frontotemporal lobar degeneration ...
Frontotemporal dementia (FTD) is a neurodegenerative disease with a strong genetic basis. Understand...
Frontotemporal dementia (FTD) is a neurodegenerative disease with a strong genetic basis. Understand...
Several causative gene mutations have been identified in frontotemporal lobar degeneration (FTLD), i...
International audienceThe preclinical stage of frontotemporal lobar degeneration (FTLD) is not well ...
Mutations in the progranulin (PGRN) gene have been recently demonstrated as a cause of frontotempora...
International audienceMutations in the progranulin (GRN) gene are responsible for 20% of familial ca...
In genetic frontotemporal dementia, cross-sectional studies have identified profiles of presymptomat...
Loss-of-function mutations in the progranulin gene (GRN) are one of the major causes of familial fro...
Frontotemporal dementia (FTD) is a heterogeneous group of neurodegenerative disorders with both spor...
Frontotemporal dementia (FTD) is a heterogeneous group of neurodegenerative disorders with both spor...
AbstractNeural network breakdown is a key issue in neurodegenerative disease, but the mechanisms are...
White matter hyperintensities (WMH) are often seen on MRI brain scans in frontotemporal dementia (FT...
Granulin (GRN) mutations have been identified as a major cause of frontotemporal lobar degeneration ...
Frontotemporal dementia (FTD) is a neurodegenerative disease with a strong genetic basis. Understand...
Frontotemporal dementia (FTD) is a neurodegenerative disease with a strong genetic basis. Understand...
Several causative gene mutations have been identified in frontotemporal lobar degeneration (FTLD), i...
International audienceThe preclinical stage of frontotemporal lobar degeneration (FTLD) is not well ...