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PLoS ONE, ISSN 1932-6203, 08/2012, Volume 7, Issue 8, p. e43993
There is increasing evidence that amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) lie on a clinical, pathological and genetic continuum... 
HEXANUCLEOTIDE REPEAT EXPANSION | LOBAR DEGENERATION | ATROPHY | TDP-43 | MULTIDISCIPLINARY SCIENCES | WHOLE-BRAIN | CLINICAL CHARACTERISTICS | COGNITIVE IMPAIRMENT | PATTERNS | BEHAVIORAL VARIANT | C9ORF72 | Frontotemporal Dementia - physiopathology | Amyotrophic Lateral Sclerosis - physiopathology | Brain - physiopathology | Humans | Middle Aged | Prefrontal Cortex - physiopathology | Male | Motor Cortex - physiopathology | Behavior - physiology | Cognition | Case-Control Studies | Motor Cortex - pathology | Diffusion Tensor Imaging | Prefrontal Cortex - pathology | Atrophy | Amyotrophic Lateral Sclerosis - pathology | Pyramidal Tracts - physiopathology | Brain - pathology | Female | Pyramidal Tracts - pathology | Frontotemporal Dementia - pathology | Amyotrophic lateral sclerosis | Research | Medical case management | Frontotemporal dementia | Neuroimaging | Brain | Neurosciences | Disease | Cortex (motor) | Substantia grisea | Apathy | Neurodegeneration | Cortex (frontal) | Imaging | Dementia disorders | Degeneration | Behavior | Cortex (temporal) | Cortex (prefrontal) | Temporal lobe | Cortex (cingulate) | Medical imaging | Magnetic resonance | Pyramidal tracts | Substantia alba | Disease control | Patients | Lobes | Studies | Neurology | Brain research | Magnetic resonance imaging | Cognition & reasoning | Morphometry | Dementia
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PLoS ONE, ISSN 1932-6203, 04/2012, Volume 7, Issue 4, p. e35241
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