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

Atypical presentation of probable Creutzfeldt-Jakob disease associated with anti-Zic4 antibody: Literature review of neuronal antibodies in Creutzfeldt-Jakob disease.

Clinical neurology and neurosurgery - 1 May 2018

Salazar Richard

Abstract excerpt

INTRODUCTION: Sporadic Creutzfeldt-Jakob disease is a prion disease characterized by rapidly progressive dementia, ataxia and myoclonus. Atypical phenotype masquerading as stroke, movement disorders or autoimmune encephalitis have been described. Here, I report a probable case of sCJD with an atypical presentation associated with anti-Zic4 antibody and review the literature of neuronal antibodies in CJD. CASE...

Read the complete abstract on PubMed

Topics

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

Share to Autoantibodies
Share to Brain
Share to Creutzfeldt-Jakob Syndrome

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Diagnosis, Differential

Share to Encephalitis

Share to Hashimoto Disease

Share to Nerve Tissue Proteins

Share to Probability

Source

Identifiers

PMID: 29525731
DOI: 10.1016/j.clineuro.2018.02.043

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

Atypical presentation of probable Creutzfeldt-Jakob disease associated with anti-Zic4 antibody: Literature review of neuronal antibodies in Creutzfeldt-Jakob disease.PMID 29525731Read ↗

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

Clinical Utility and Correlates of Cerebrospinal Fluid 14-3-3 Protein in the Evaluation of Rapid Progressive DementiaSemantic proximity Read ↗

A Unique Case of Genetic Creutzfeldt-Jakob Disease (E200K Mutation) with CSF-restricted Anti Myelin Oligodendrocyte Glycoprotein Antibody.Semantic proximity Read ↗

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

Unusual presentations in patients with E200K familial Creutzfeldt-Jakob disease.Semantic proximity Read ↗

The epidemiological, clinical, and laboratory features of sporadic Creutzfeldt-Jakob disease patients in China: surveillance data from 2006 to 2010.Semantic proximity Read ↗

New variant Creutzfeldt-Jakob disease: neurological features and diagnostic tests.Semantic proximity Read ↗

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

Creutzfeldt-Jakob Disease with Initial Typical Parkinsonism Precipitated by COVID-19? A Case ReportSemantic proximity Read ↗

Clinical diagnosis and differential diagnosis of CJD and vCJD. With special emphasis on laboratory tests.Semantic proximity Read ↗

14-3-3 CSF levels in sporadic Creutzfeldt-Jakob disease differ across molecular subtypes.Semantic proximity Read ↗

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