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Article

The metabolic signature of C9ORF72-related ALS: FDG PET comparison with nonmutated patients.

European journal of nuclear medicine and molecular imaging - 1 May 2014

Cistaro Angelina, Pagani Marco, Montuschi Anna, Calvo Andrea, Moglia Cristina, Canosa Antonio, Restagno Gabriella, Brunetti Maura, Traynor Bryan J, Nobili Flavio, Carrara Giovanna, Fania Piercarlo, Lopiano Leonardo, Valentini M Consuelo, Chiò Adriano

Abstract excerpt

PURPOSE: Recently, a GGGGCC hexanucleotide repeat expansion in the C9ORF72 gene, located on chromosome 9p21 has been demonstrated to be the commonest cause of familial amyotrophic lateral sclerosis (ALS) and to account for 5 to 10 % of apparently sporadic ALS. Relatively little is known about the...

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Identifiers

PMID: 24445987
DOI: 10.1007/s00259-013-2667-5
PMCID: PMC8957062

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24445987-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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