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

Seropositive polyarthritis and diffuse lymphadenopathy associated with PRKCD mutation.

Rheumatology (Oxford, England) - 3 May 2024

Papa Riccardo, Schena Francesca, Corcione Anna, Bocca Paola, Drago Enrico, Malattia Clara, Grossi Alice, Ceccherini Isabella, Gattorno Marco

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 Arthritis
Share to Mutation

Source

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 38065692
DOI: 10.1093/rheumatology/kead639
PMCID: PMC11147532

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 25 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 8 closest

Seropositive polyarthritis and diffuse lymphadenopathy associated with PRKCD mutation.PMID 38065692Read ↗

Protein Kinase C-Delta Defect in Autoimmune Lymphoproliferative Syndrome-Like Disease: First Case from the National Iranian Registry and Review of the Literature.Semantic proximity Read ↗

PRKDC mutations associated with immunodeficiency, granuloma, and autoimmune regulator-dependent autoimmunity.Semantic proximity Read ↗

Sirolimus is effective in autoimmune lymphoproliferative syndrome-type III: A pedigree case report with homozygous variation PRKCD.Semantic proximity Read ↗

Phenotypic Variability in PRKCD: a Review of the LiteratureSemantic proximity Read ↗

Risk of Cancer in Patients With Primary Sjögren's Disease and Their Relatives.Semantic proximity Read ↗

A case of rheumatoid arthritis associated with SMAD3 gene mutation: a new clinical entity?Semantic proximity Read ↗

A 32-year-old female with relapsing polychondritis and common variable immunodeficiency due to a monogenic mutation in NFKB2.Semantic proximity Read ↗

Protein Kinase C δ: a Gatekeeper of Immune Homeostasis.Semantic proximity Read ↗

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