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 Clinical Stages of Sporadic Creutzfeldt-Jakob Disease with Met/Met Genotype in Korean Patients.

European neurology - 1 Jan 2016

Park So Young, Wang Min Jeong, Jang Jae-Won, Park Young Ho, Lim Jae-Sung, Youn Young Chul, Kim Jungeun, Kim SangYun

Abstract excerpt

BACKGROUND: Clinical diagnosis of sporadic Creutzfeldt-Jakob disease (sCJD) is currently based on changes occurring in the late disease stages, which limits early-stage detection. Therefore, we investigated the disease course from the vague symptomatic to the terminal phase. METHODS: We retrospectively reviewed 36 sCJD patient records, classifying the disease progression into 4 stages based on clinical...

Read the complete abstract on PubMed

Topics

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

Share to 14-3-3 Proteins
Share to Aged
Share to Creutzfeldt-Jakob Syndrome

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Diffusion Magnetic Resonance Imaging

Share to Disease Progression

Share to Electroencephalography

Share to Genotype

Source

Identifiers

PMID: 27104644
DOI: 10.1159/000445768

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 Clinical Stages of Sporadic Creutzfeldt-Jakob Disease with Met/Met Genotype in Korean Patients.PMID 27104644Read ↗

The advances in the early and accurate diagnosis of Creutzfeldt-Jakob disease and other prion diseases: where are we today?Semantic proximity Read ↗

Clinical and laboratory features of 14 young Chinese probable sCJD patients.Semantic proximity Read ↗

Clinical and Genetic Characteristics of the Heidenhain Variant of Creutzfeldt-Jakob Disease.Semantic proximity Read ↗

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

[Creutzfeldt-Jakob Disease].Semantic proximity Read ↗

Current clinical diagnosis in Creutzfeldt-Jakob disease: identification of uncommon variants.Semantic proximity Read ↗

Clinical course in young patients with sporadic 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 ↗

The Phenotypic Spectrum of Sporadic Creutzfeldt-Jakob Disease Cortical Subtype.Semantic proximity Read ↗

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

Sporadic human prion diseases: molecular insights and diagnosis.Semantic proximity Read ↗

EEG - Imaging Evolution of the MV2 Subtype of Sporadic Creutzfeldt-Jakob Disease During the two-Year Course of the Disease.Semantic proximity Read ↗

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