Objective: To investigate possible effects of the C9orf72 repeat expansion before disease onset, we assessed brain morphology in asymptomatic carriers. Methods: Aiming to diminish the effects of genetic variation between subjects, apart from the C9orf72 repeat expansion, 16 carriers of the repeat expansion were compared with 23 noncarriers from the same large family with a history of amyotrophic lateral sclerosis (ALS). Cortical thickness, subcortical volumes, and white matter connectivity, as assessed from high-resolution T1-weighted and diffusion-weighted MRIs, were evaluated. For comparison, we included 14 C9orf72 carriers with ALS and 28 healthy, unrelated controls. Results: We found temporal, parietal, and occipital regions to be thinn...
BACKGROUND AND OBJECTIVES: The C9orf72 expansion is the most common genetic cause of frontotemporal ...
Background: The neuropathology of patients with frontotemporal dementia (FTD) or amyotrophic lateral...
Background: The neuropathology of patients with frontotemporal dementia (FTD) or amyotrophic lateral...
BACKGROUND: In patients with a C9orf72 repeat expansion (C9+), a neuroimaging phenotype with widespr...
Expansion mutations in the C9orf72 gene may cause amyotrophic lateral sclerosis (ALS), frontotempora...
AbstractExpansion mutations in the C9orf72 gene may cause amyotrophic lateral sclerosis (ALS), front...
Objective: Expansions of a hexanucleotide repeat in C9ORF72 are a common cause of familial amyotroph...
International audienceImportance Presymptomatic carriers of chromosome 9 open reading frame 72 (C9o...
Background: ALS patients with hexanucleotide expansion in C9orf72 are characterized by a specific cl...
International audienceOBJECTIVE:C9orf72 hexanucleotide repeats expansions account for almost half of...
Hexanucleotide repeat expansions in C9ORF72 are the most common known genetic cause of familial and ...
Objective To discern presymptomatic changes in brain structure or function using advanced MRI in car...
Objective: To understand the progressive nature of amyotrophic lateral sclerosis (ALS) by investigat...
OBJECTIVE: To understand the progressive nature of amyotrophic lateral sclerosis (ALS) by investigat...
Objective: To investigate cognitive function, gray matter volume, and white matter integrity in the ...
BACKGROUND AND OBJECTIVES: The C9orf72 expansion is the most common genetic cause of frontotemporal ...
Background: The neuropathology of patients with frontotemporal dementia (FTD) or amyotrophic lateral...
Background: The neuropathology of patients with frontotemporal dementia (FTD) or amyotrophic lateral...
BACKGROUND: In patients with a C9orf72 repeat expansion (C9+), a neuroimaging phenotype with widespr...
Expansion mutations in the C9orf72 gene may cause amyotrophic lateral sclerosis (ALS), frontotempora...
AbstractExpansion mutations in the C9orf72 gene may cause amyotrophic lateral sclerosis (ALS), front...
Objective: Expansions of a hexanucleotide repeat in C9ORF72 are a common cause of familial amyotroph...
International audienceImportance Presymptomatic carriers of chromosome 9 open reading frame 72 (C9o...
Background: ALS patients with hexanucleotide expansion in C9orf72 are characterized by a specific cl...
International audienceOBJECTIVE:C9orf72 hexanucleotide repeats expansions account for almost half of...
Hexanucleotide repeat expansions in C9ORF72 are the most common known genetic cause of familial and ...
Objective To discern presymptomatic changes in brain structure or function using advanced MRI in car...
Objective: To understand the progressive nature of amyotrophic lateral sclerosis (ALS) by investigat...
OBJECTIVE: To understand the progressive nature of amyotrophic lateral sclerosis (ALS) by investigat...
Objective: To investigate cognitive function, gray matter volume, and white matter integrity in the ...
BACKGROUND AND OBJECTIVES: The C9orf72 expansion is the most common genetic cause of frontotemporal ...
Background: The neuropathology of patients with frontotemporal dementia (FTD) or amyotrophic lateral...
Background: The neuropathology of patients with frontotemporal dementia (FTD) or amyotrophic lateral...