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

Case report of a patient with VEXAS syndrome.

Medicine - 29 Dec 2023

Tsourveloudis Ioannis, Georgiadi Eleni C, Vatalis Georgios, Kotsi Paraskevi

Abstract excerpt

RATIONALE: Hematological malignancies have always been a challenge for scientists because there is a constant need to better define these entities. Myelodysplastic syndromes (MDS) are clonal hematopoietic disorders characterized by ineffective hematopoiesis. Cytogenetics and molecular findings are a prerequisite for these syndromes as they confirm the clonal nature of the disease. However, MDS is often linked to...

Read the complete abstract on PubMed

Topics

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

Share to Affect
Share to Hematologic Neoplasms
Share to Inflammation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Myelodysplastic Syndromes

Share to Skin Diseases, Genetic

Source

Open in PubMed Open full text

Identifiers

PMID: 38206689
DOI: 10.1097/MD.0000000000036738
PMCID: PMC10754568

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

Case report of a patient with VEXAS syndrome.PMID 38206689Read ↗

VEXAS syndrome: Clinical, hematologic features and a practical approach to diagnosis and management.Semantic proximity Read ↗

How I diagnose and manage VEXAS syndrome.Semantic proximity Read ↗

Looking beyond VEXAS: Coexistence of undifferentiated systemic autoinflammatory disease and myelodysplastic syndrome.Semantic proximity Read ↗

VEXAS syndrome: a new paradigm for adult-onset monogenic autoinflammatory diseases.Semantic proximity Read ↗

Further characterization of clinical and laboratory features in VEXAS syndrome: large-scale analysis of a multicentre case series of 116 French patients.Semantic proximity Read ↗

American College of Rheumatology Guidance Statement for Diagnosis and Management of VEXAS Developed by the International VEXAS Working Group Expert Panel.Semantic proximity Read ↗

VEXAS syndrome: An update.Semantic proximity Read ↗

VEXAS syndrome: relapsing polychondritis and myelodysplastic syndrome with associated immunoglobulin A vasculitisSemantic proximity Read ↗

Clinical features in VEXAS syndrome: a systematic review.Semantic proximity Read ↗

VEXAS syndrome: Clinical manifestations, diagnosis, and treatment.Semantic proximity Read ↗

Case report: diagnosis of VEXAS syndrome in a patient with therapy-resistant large vessel vasculitis.Semantic proximity Read ↗

Ocular and orbital manifestations in VEXAS syndrome.Semantic proximity Read ↗

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