Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

The imaging appearance of Creutzfeldt-Jakob disease caused by the E200K mutation.

Magnetic resonance imaging - 1 Nov 2006

Fulbright Robert K, Kingsley Peter B, Guo Xiaodong, Hoffmann Chen, Kahana Esther, Chapman Joab C, Prohovnik Isak

Abstract excerpt

The E200K mutation on chromosome 20 can cause familial Creutzfeldt-Jakob disease (CJD). Patients with this mutation are clinically similar to those with sporadic CJD, but their imaging features are not well documented. We report here the quantitative and qualitative evaluation of the magnetic resonance (MR) imaging characteristics of this unique group of patients using three-dimensional spoiled gradient recalled...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Brain
Share to Chromosomes, Human, Pair 20

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Creutzfeldt-Jakob Syndrome

Share to Diffusion Magnetic Resonance Imaging

Share to Israel

Share to Magnetic Resonance Spectroscopy

Share to Mutation

Source

Identifiers

PMID: 17071334
DOI: 10.1016/j.mri.2006.07.001

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The imaging appearance of Creutzfeldt-Jakob disease caused by the E200K mutation.PMID 17071334Read ↗

Magnetic resonance imaging in E200K and V210I mutations of the prion protein gene.Semantic proximity Read ↗

MR imaging of familial Creutzfeldt-Jakob disease: a blinded and controlled study.Semantic proximity Read ↗

White matter abnormalities in healthy E200K carriers may serve as an early biomarker for genetic Creutzfeldt-Jakob disease (gCJD).Semantic proximity Read ↗

Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease.Semantic proximity Read ↗

MRI lesion profiles in sporadic Creutzfeldt-Jakob disease.Semantic proximity Read ↗

Diffusion-weighted MRI in familial Creutzfeldt-Jakob disease with the codon 200 mutation in the prion protein gene.Semantic proximity Read ↗

Clinical radiological correlation in E200K familial Creutzfeldt-Jakob disease.Semantic proximity Read ↗

White Matter Integrity Involvement in Preclinical Stage of Familial Creutzfeldt-Jakob Disease: A Diffusion Tensor Imaging StudySemantic proximity Read ↗

Familial Creutzfeldt-Jakob disease with the E200K mutation: longitudinal neuroimaging from asymptomatic to symptomatic CJD.Semantic proximity Read ↗

Familial Creutzfeldt-Jakob disease homozygous to the E200K mutation: clinical characteristics and disease course.Semantic proximity Read ↗

Periodic sharp wave complexes identify a distinctive phenotype in Creutzfeldt-Jacob disease.Semantic proximity Read ↗

An atypical phenotype of CJD associated with the E200K mutation in the prion protein gene.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.