Background: In patients with a C9orf72 repeat expansion (C9+), a neuroimaging phenotype with widespread structural cerebral changes has been found. We aimed to investigate the specificity of this neuroimaging phenotype in patients with amyotrophic lateral sclerosis (ALS). Methods: 156 C9- and 14 C9+ patients with ALS underwent high-resolution T1-weighted MRI; a subset (n=126) underwent diffusion-weighted imaging. Cortical thickness, subcortical volumes and white matter integrity were compared between C9+ and C9-patients. Using elastic net logistic regression, a model defining the neuroimaging phenotype of C9+ was determined and applied to C9-patients with ALS. Results: C9+ patients showed cortical thinning outside the precentral gyrus, exte...
Background: Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder clinically character...
Clinical and neuropathological characteristics associated with G4C2 repeat expansions in chromosome ...
The papers selected represent characterisation of amyotrophic lateral sclerosis (ALS) patients belon...
BACKGROUND: In patients with a C9orf72 repeat expansion (C9+), a neuroimaging phenotype with widespr...
Background: ALS patients with hexanucleotide expansion in C9orf72 are characterized by a specific cl...
Expansion mutations in the C9orf72 gene may cause amyotrophic lateral sclerosis (ALS), frontotempora...
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...
AbstractExpansion mutations in the C9orf72 gene may cause amyotrophic lateral sclerosis (ALS), front...
Objective: To investigate possible effects of the C9orf72 repeat expansion before disease onset, we ...
Objective: Expansions of a hexanucleotide repeat in C9ORF72 are a common cause of familial amyotroph...
AbstractAn expanded hexanucleotide repeat in the C9orf72 gene is the most common genetic cause of am...
International audienceBackground: In familial amyotrophic lateral sclerosis (ALS) cases, the presenc...
The GGGGCC (G4C2) repeat expansion in C9ORF72 is the most common cause of familial amyotrophic later...
Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are part of the same disease s...
Background: Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder clinically character...
Clinical and neuropathological characteristics associated with G4C2 repeat expansions in chromosome ...
The papers selected represent characterisation of amyotrophic lateral sclerosis (ALS) patients belon...
BACKGROUND: In patients with a C9orf72 repeat expansion (C9+), a neuroimaging phenotype with widespr...
Background: ALS patients with hexanucleotide expansion in C9orf72 are characterized by a specific cl...
Expansion mutations in the C9orf72 gene may cause amyotrophic lateral sclerosis (ALS), frontotempora...
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...
AbstractExpansion mutations in the C9orf72 gene may cause amyotrophic lateral sclerosis (ALS), front...
Objective: To investigate possible effects of the C9orf72 repeat expansion before disease onset, we ...
Objective: Expansions of a hexanucleotide repeat in C9ORF72 are a common cause of familial amyotroph...
AbstractAn expanded hexanucleotide repeat in the C9orf72 gene is the most common genetic cause of am...
International audienceBackground: In familial amyotrophic lateral sclerosis (ALS) cases, the presenc...
The GGGGCC (G4C2) repeat expansion in C9ORF72 is the most common cause of familial amyotrophic later...
Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are part of the same disease s...
Background: Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder clinically character...
Clinical and neuropathological characteristics associated with G4C2 repeat expansions in chromosome ...
The papers selected represent characterisation of amyotrophic lateral sclerosis (ALS) patients belon...