Novel evidence of phenotypical variability in the hexanucleotide repeat expansion in chromosome 9

Journal of Alzheimer's Disease

Volumn 35, Issue 3, 2013, Pages 455-462

  Cerami, Chiara ^a,b   Marcone, Alessandra ^a   Galimberti, Daniela ^c   Zamboni, Michele ^a   Fenoglio, Chiara ^c   Serpente, Maria ^c   Scarpini, Elio ^c   Cappa, Stefano F ^a,b  

^a SAN RAFFAELE HOSPITAL   (Italy)

^b VITA SALUTE SAN RAFFAELE UNIVERSITY   (Italy)

^c UNIVERSITY OF MILAN   (Italy)

Author keywords

C9ORF72 mutation; frontotemporal dementia; frontotemporal lobar degeneration; mild cognitive impairment; motor neuron disorders; semantic dementia

Indexed keywords

DONEPEZIL; FLUORODEOXYGLUCOSE F 18; TECHNETIUM 99M;

ADULT; AGED; ALZHEIMER DISEASE; AMYOTROPHIC LATERAL SCLEROSIS; APATHY; ARTICLE; CHROMOSOME 9; FAMILY HISTORY; FEMALE; FRONTAL VARIANT FRONTOTEMPORAL DEMENTIA; FRONTOTEMPORAL DEMENTIA; GENE MUTATION; GENETIC HETEROGENEITY; GENETIC VARIABILITY; HEREDITY; HEXANUCLEOTIDE REPEAT EXPANSION; HUMAN; HYPERPHAGIA; MAJOR CLINICAL STUDY; MALE; MEMORY DISORDER; MINI MENTAL STATE EXAMINATION; MOTOR NEURON DISEASE; NEUROIMAGING; NEUROPSYCHOLOGICAL TEST; NUCLEAR MAGNETIC RESONANCE IMAGING; NUCLEOTIDE REPEAT; OPEN READING FRAME; PHENOTYPE; POSITRON EMISSION TOMOGRAPHY; PRIORITY JOURNAL; PSYCHOSOCIAL WITHDRAWAL; SCREENING TEST; SEMANTIC DEMENTIA; SINGLE PHOTON EMISSION COMPUTER TOMOGRAPHY; SYMPTOM;

EID: 84880202372     PISSN: 13872877     EISSN: 18758908     Source Type: Journal    
DOI: 10.3233/JAD-122302     Document Type: Article

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