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

Eye movement abnormalities in a patient with Zellweger spectrum disorder.

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology - 1 Jun 2016

Rosini F, Vinciguerra C, Mignarri A, Di Giovanni M, Federico A, Rufa A

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Membrane Proteins
Share to Mutation
Share to Ocular Motility Disorders
Share to Reaction Time

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Zellweger Syndrome

Source

Identifiers

PMID: 26850714
DOI: 10.1007/s10072-016-2499-8

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Eye movement abnormalities in a patient with Zellweger spectrum disorder.PMID 26850714Read ↗

Ophthalmic Features of Children Not Yet Diagnosed with Alstrom Syndrome.Semantic proximity Read ↗

CLINICAL EVALUATION OF GENETIC DISEASES OF THE EYE.Semantic proximity Read ↗

Spectrum of Ophthalmic Disorders in Prader-Willi Syndrome: Implications for Early Screening and Multidisciplinary ManagementSemantic proximity Read ↗

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

A Case of Chorea with Slow Saccades Caused by NKX2-1 Mutation.Semantic proximity Read ↗

Eye signs in a child with ROBO3 gene mutation.Semantic proximity Read ↗

Congenital and Genetic Ocular Motility Disorders: Update and Considerations.Semantic proximity Read ↗

Ophthalmic pathology of genotypically confirmed von Hippel Lindau disease type 1.Semantic proximity Read ↗

Benign hereditary chorea: more than meets the eye.Semantic proximity Read ↗

A case of de Barsy syndrome with a severe eye phenotype.Semantic proximity Read ↗

Abnormal saccadic eye movements associated with positive family history schizophrenics.Semantic proximity Read ↗

Chorea.Semantic proximity Read ↗

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