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

Clinical and MRI phenotype of children with MOG antibodies.

Multiple sclerosis (Houndmills, Basingstoke, England) - 1 Feb 2016

Fernandez-Carbonell Cristina, Vargas-Lowy David, Musallam Alexander, Healy Brian, McLaughlin Katherine, Wucherpfennig Kai W, Chitnis Tanuja

Abstract excerpt

OBJECTIVE: To investigate the clinical and magnetic resonance imaging (MRI) features of anti-myelin oligodendrocyte glycoprotein (MOG) antibody-seropositive pediatric demyelinating syndromes. METHODS: Serum samples collected from 74 children with suspected demyelinating disorders whom were being followed at Massachusetts General Hospital were incubated with control green fluorescent protein (GFP)- and...

Read the complete abstract on PubMed

Topics

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

Share to Aquaporin 4
Share to Autoantibodies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Demyelinating Diseases

Share to Flow Cytometry

Share to Multiple Sclerosis

Share to Myelin-Oligodendrocyte Glycoprotein

Share to Neuromyelitis Optica

Share to Spinal Cord

Source

Open in PubMed Open full text

Identifiers

PMID: 26041801
DOI: 10.1177/1352458515587751
PMCID: PMC4669239

Genes

MOG
AQP4

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clinical and MRI phenotype of children with MOG antibodies.PMID 26041801Read ↗

E.U. paediatric MOG consortium consensus: Part 1 - Classification of clinical phenotypes of paediatric myelin oligodendrocyte glycoprotein antibody-associated disorders.Semantic proximity Read ↗

Anti-MOG antibodies are present in a subgroup of patients with a neuromyelitis optica phenotypeSemantic proximity Read ↗

'Leukodystrophy-like' phenotype in children with myelin oligodendrocyte glycoprotein antibody-associated disease.Semantic proximity Read ↗

Myelin Oligodendrocyte Glycoprotein: Deciphering a Target in Inflammatory Demyelinating DiseasesSemantic proximity Read ↗

Less common phenotypes of myelin oligodendrocyte glycoprotein antibody-related diseases in children deserve more attention.Semantic proximity Read ↗

Attack phenotypes and disease course in pediatric MOGAD.Semantic proximity Read ↗

Anti-MOG antibody: The history, clinical phenotype, and pathogenicity of a serum biomarker for demyelination.Semantic proximity Read ↗

Myelin Oligodendrocyte Glycoprotein–Associated DisordersSemantic proximity Read ↗

Two Pediatric Cases of Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease Predominantly Presenting as Cortical Encephalitis: A Case Report and Literature ReviewSemantic proximity Read ↗

E.U. paediatric MOG consortium consensus: Part 4 - Outcome of paediatric myelin oligodendrocyte glycoprotein antibody-associated disorders.Semantic proximity Read ↗

Progressive Leukodystrophy-Like Demyelinating Syndromes with MOG-Antibodies in Children: A Rare Under-Recognized Phenotype.Semantic proximity Read ↗

Assessment of international MOGAD diagnostic criteria in patients with overlapping MOG-associated disease and multiple sclerosis phenotypes.Semantic proximity Read ↗

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