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

Ocular Motor Abnormalities in Anti-IgLON5 Disease.

Frontiers in immunology - 1 Jan 2021

Macher Stefan, Milenkovic Ivan, Zrzavy Tobias, Höftberger Romana, Seidel Stefan, Berger-Sieczkowski Evelyn, Berger Thomas, Rommer Paulus S, Wiest Gerald

Abstract excerpt

Objective: Anti-IgLON5 disease forms an interface between neuroinflammation and neurodegeneration and includes clinical phenotypes that are often similar to those of neurodegenerative diseases. An early diagnosis of patients with anti-IgLON5 disease and differentiation from neurodegenerative diseases is necessary and may have therapeutic implications. Methods: In our small sample size study we investigated...

Read the complete abstract on PubMed

Topics

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

Share to Autoimmune Diseases of the Nervous System
Share to Electrooculography

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Neuroinflammatory Diseases

Share to Nystagmus, Pathologic

Share to Ocular Motility Disorders

Share to Reflex, Abnormal

Share to Saccades

Share to Video Recording

Source

Open in PubMed Open full text

Identifiers

PMID: 34659261
DOI: 10.3389/fimmu.2021.753856
PMCID: PMC8514941

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Ocular Motor Abnormalities in Anti-IgLON5 Disease.PMID 34659261Read ↗

Motor-neuron-disease-like phenotype associated with IgLON5 disease.Semantic proximity Read ↗

Progressive supranuclear palsy: current approach and challenges to diagnosis and treatment.Semantic proximity Read ↗

Ocular motor biomarkers in Niemann-Pick disease type C: A prospective cross-sectional multicontinental study in 72 patientsSemantic proximity Read ↗

Progressive Supranuclear Palsy: an Update.Semantic proximity Read ↗

Oculomotor phenotypes and longitudinal video-oculography dynamics in anti-GAD65 antibody-associated neurological syndromes: a case series and literature review.Semantic proximity Read ↗

The phenotypic spectrum of progressive supranuclear palsy.Semantic proximity Read ↗

Ocular Motor and Vestibular Profile in Spinocerebellar Ataxia Type 27B: Toward a Practical Bedside Diagnostic FrameworkSemantic proximity Read ↗

Abnormal Vertical Eye Movements as a Clue for Diagnosis of Niemann-Pick Type C.Semantic proximity Read ↗

Oculomotor deficits in spinocerebellar ataxia type 3: Potential biomarkers of preclinical detection and disease progression.Semantic proximity Read ↗

No anti-IgLON5 antibody in carefully diagnosed PSP patients with "atypical" or variant clinical features.Semantic proximity Read ↗

Eye movement biomarkers allow for the definition of phenotypes in Gaucher DiseaseSemantic proximity Read ↗

Quantitative Oculomotor Assessment in Hereditary Ataxia: Discriminatory Power, Correlation with Severity Measures, and Recommended Parameters for Specific Genotypes.Semantic proximity Read ↗

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