Neuroimaging studies of familial Alzheimer's disease allow investigation of the disease process before clinical onset. We performed semi-automated MRI analysis to evaluate cortical thickness (CTh), grey matter (GM) volumes, and GM diffusivity indexes in PSEN1 mutation carriers (MC). We recruited 11 MC from 4 families with PSEN1 mutations (L286P, M139T, K239N) and 6 familial and 12 non-familial healthy controls. MC were classified as either asymptomatic (n=6) or symptomatic (n=5). Subjects underwent structural and diffusion-weighted 3-Tesla MRI scanning. CTh and GM volumes of subcortical structures and diffusivity indexes were calculated and group comparisons were performed. Structural images were reanalyzed with voxel-based morphometry meth...
Mutations in the granulin gene (GRN) cause familial frontotemporal dementia. Understanding the struc...
Noninvasive biomarkers of early neuronal injury may help identify cognitively normal individuals at ...
In this study, we analyzed differences in cortical thickness (CTH) between healthy controls (HC), su...
PSEN1 mutations are the most frequent cause of autosomal dominant Alzheimer's disease (ADAD), and sh...
BACKGROUND: There is increasing interest in improving understanding of the timing and nature of earl...
BACKGROUND: MRI in presymptomatic autosomal dominant Alzheimer's disease mutation carriers (MC) prov...
Amyloid imaging studies of presymptomatic familial Alzheimer’s disease have revealed the striatum an...
OBJECTIVE: To identify a cortical signature pattern of cortical thinning in familial Alzheimer disea...
Presenilin 1 (PSEN1) mutations cause autosomal dominant familial Alzheimer's disease (FAD). PSEN1 mu...
Presenilin 1 (PS1) mutation carriers provide the opportunity to asses early features of neurodegener...
Presenilin 1 (PS1) mutation carriers provide the opportunity to asses early features of neurodegener...
White matter hyperintensities (WMHs) are areas of increased signal on T2-weighted magnetic resonance...
Mutations in the granulin gene (GRN) cause familial frontotemporal dementia. Understanding the struc...
OBJECTIVE: To assess regional patterns of gray and white matter atrophy in familial Alzheimer diseas...
Objectives To investigate the global cortical and regional quantitative features of cortical neural ...
Mutations in the granulin gene (GRN) cause familial frontotemporal dementia. Understanding the struc...
Noninvasive biomarkers of early neuronal injury may help identify cognitively normal individuals at ...
In this study, we analyzed differences in cortical thickness (CTH) between healthy controls (HC), su...
PSEN1 mutations are the most frequent cause of autosomal dominant Alzheimer's disease (ADAD), and sh...
BACKGROUND: There is increasing interest in improving understanding of the timing and nature of earl...
BACKGROUND: MRI in presymptomatic autosomal dominant Alzheimer's disease mutation carriers (MC) prov...
Amyloid imaging studies of presymptomatic familial Alzheimer’s disease have revealed the striatum an...
OBJECTIVE: To identify a cortical signature pattern of cortical thinning in familial Alzheimer disea...
Presenilin 1 (PSEN1) mutations cause autosomal dominant familial Alzheimer's disease (FAD). PSEN1 mu...
Presenilin 1 (PS1) mutation carriers provide the opportunity to asses early features of neurodegener...
Presenilin 1 (PS1) mutation carriers provide the opportunity to asses early features of neurodegener...
White matter hyperintensities (WMHs) are areas of increased signal on T2-weighted magnetic resonance...
Mutations in the granulin gene (GRN) cause familial frontotemporal dementia. Understanding the struc...
OBJECTIVE: To assess regional patterns of gray and white matter atrophy in familial Alzheimer diseas...
Objectives To investigate the global cortical and regional quantitative features of cortical neural ...
Mutations in the granulin gene (GRN) cause familial frontotemporal dementia. Understanding the struc...
Noninvasive biomarkers of early neuronal injury may help identify cognitively normal individuals at ...
In this study, we analyzed differences in cortical thickness (CTH) between healthy controls (HC), su...