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Article

Combined FDG and raclopride PET study in a case of ALS with the R521C FUS gene mutation.

Journal of neurology - 1 Feb 2012

Kono Satoshi, Ouchi Yasuomi, Terada Tatsuhiro, Suzuki Makiko, Yagi Shunsuke, Miyajima Hiroaki

Abstract excerpt

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Topics

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Share to Amyotrophic Lateral Sclerosis
Share to Fluorodeoxyglucose F18
Share to FUS gene
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Positron-Emission Tomography

Share to Radiopharmaceuticals

Share to RNA-Binding Protein FUS

Source

Identifiers

PMID: 21761142
DOI: 10.1007/s00415-011-6168-9

Genes

FUS

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

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Combined FDG and raclopride PET study in a case of ALS with the R521C FUS gene mutation.PMID 21761142Read ↗

Molecular tracers for the PET and SPECT imaging of diseaseSemantic proximity Read ↗

Pilot PET Study to Assess the Functional Interplay Between ABCB1 and ABCG2 at the Human Blood-Brain Barrier.Semantic proximity Read ↗

FDG PET Findings in Rare Brain Sodium Channelopathy Associated with SCN2A Gene Mutation.Semantic proximity Read ↗

FUS mutations in frontotemporal lobar degeneration with amyotrophic lateral sclerosis.Semantic proximity Read ↗

An autopsy case of familial amyotrophic lateral sclerosis with FUS R521G mutation.Semantic proximity Read ↗

Amyotrophic lateral sclerosis caused by FUS mutations: advances with broad implicationsSemantic proximity Read ↗

Novel FUS mutations identified through molecular screening in a large cohort of familial and sporadic amyotrophic lateral sclerosis.Semantic proximity Read ↗

G507D mutation in FUS gene causes familial amyotrophic lateral sclerosis with a specific genotype-phenotype correlation.Semantic proximity Read ↗

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