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

Chronic cutaneous pustulosis due to a 175-kb deletion on chromosome 2q13: excellent response to anakinra.

Archives of dermatology - 1 Mar 2012

Brau-Javier Cristina N, Gonzales-Chavez Jose, Toro Jorge R

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 Genes, Recessive
Share to Antirheumatic Agents
Share to Chromosome Deletion
Share to Chromosomes, Human, Pair 2

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hereditary Autoinflammatory Diseases

Share to Interleukin 1 Receptor Antagonist Protein

Share to Psoriasis

Source

Open in PubMed Open full text

Identifiers

PMID: 22431772
DOI: 10.1001/archdermatol.2011.2857
PMCID: PMC3313085

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

Chronic cutaneous pustulosis due to a 175-kb deletion on chromosome 2q13: excellent response to anakinra.PMID 22431772Read ↗

Common cutaneous signs unmasking a severe hematological disorder: GATA2 deficiency.Semantic proximity Read ↗

Hailey-Hailey disease successfully treated with tralokinumab and literature review of successful treatment with dupilumabSemantic proximity Read ↗

Majeed syndrome: description of a novel mutation and therapeutic response to bisphosphonates and IL-1 blockade with anakinraSemantic proximity Read ↗

A transient epidermolysis bullosa simplex-like phenotype associated with bexarotene treatment in a G138E KRT5 heterozygote.Semantic proximity Read ↗

Successful therapy with anakinra in a patient with generalized pustular psoriasis carrying IL36RN mutations.Semantic proximity Read ↗

Clinical and molecular characterization of a 13-year-old Indian boy with cutis laxa type 2B: Identification of two novel PYCR1 mutations by amplicon-based semiconductor exome sequencing.Semantic proximity Read ↗

Segmental stiff skin syndrome: a novel case with an interleukin-17C mutation successfully treated with secukinumab.Semantic proximity Read ↗

Targeting of Th17-related cytokines in patients with Darier DiseaseSemantic proximity Read ↗

Lasting remission of a Muckle-Wells syndrome with CIAS-1 mutation using half-dose anakinra.Semantic proximity Read ↗

Successful treatment with anakinra in generalized spiculated porokeratosis and severe hidradenitis suppurativa in a patient with MVK and MEFV mutations.Semantic proximity Read ↗

Mutation of TNFRSF13B in a child with 22q11 deletion syndrome associated with granulomatous lymphoproliferation.Semantic proximity Read ↗

Splice site and de novo variants can cause PLCG2-associated immune dysregulation with cold urticaria.Semantic proximity Read ↗

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