Functional connectivity changes show similar trajectories in autosomal dominant and sporadic Alzheimer disease

Nature Reviews Neurology

Volumn 10, Issue 9, 2014, Pages 483-

  Wood, Heather ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

AMYLOID PRECURSOR PROTEIN; PRESENILIN 1; PRESENILIN 2;

ALZHEIMER DISEASE; APP GENE; AUTOSOMAL DOMINANT ALZHEIMER DISEASE; AUTOSOMAL DOMINANT DISORDER; BRAIN REGION; CLINICAL FEATURE; DEFAULT MODE NETWORK; DISEASE COURSE; DISEASE MARKER; FAMILY HISTORY; FUNCTIONAL ANATOMY; GENE MUTATION; HETEROZYGOTE; HUMAN; ILLNESS TRAJECTORY; MILD COGNITIVE IMPAIRMENT; NOTE; ONSET AGE; PRIORITY JOURNAL; PSEN1 GENE; PSEN2 GENE; RESTING STATE NETWORK; SPORADIC ALZHEIMER DISEASE; SYMPTOM; TREATMENT RESPONSE; CONNECTOME; FEMALE; MALE; NERVE CELL NETWORK; PATHOPHYSIOLOGY; PROCEDURES;

ALZHEIMER DISEASE; CONNECTOME; FEMALE; HUMANS; MALE; NERVE NET;

EID: 84964697877     PISSN: 17594758     EISSN: 17594766     Source Type: Journal    
DOI: 10.1038/nrneurol.2014.149     Document Type: Note

References (2)

1. Thomas, J. B. et al. Functional connectivity in autosomal dominant and late-onset Alzheimer disease. JAMA Neurol. doi: 10.1001/jamaneurol.2014.1654
2. Bateman, R. J. et al. Clinical and biomarker changes in dominantly inherited Alzheimer's disease. N. Engl. J. Med. 367, 795-804 (2012) | Zhang, D. & Raichle, M. E. Disease and the brain's dark energy. Nat. Rev. Neurol. 6, 15-28 (2010)