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

Baricitinib treatment in children with COPA syndrome.

The journal of allergy and clinical immunology. In practice - 1 Aug 2024

Matucci-Cerinic Caterina, Corona Federica, Varnier Giulia Camilla, Pastore Serena, Bocca Paola, Palmeri Serena, Ravelli Angelo, Caorsi Roberta, Gattorno Marco, Tommasini Alberto, Volpi Stefano

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 Azetidines
Share to Child
Share to Child, Preschool
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Purines

Share to Pyrazoles

Share to Sulfonamides

Source

Identifiers

PMID: 38768895
DOI: 10.1016/j.jaip.2024.05.017

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

Baricitinib treatment in children with COPA syndrome.PMID 38768895Read ↗

Functional Validation of a COPA Mutation Broadens the Spectrum of COPA Syndrome.Semantic proximity Read ↗

Baricitinib treatment in a patient with a gain-of-function mutation in signal transducer and activator of transcription 1 (STAT1)Semantic proximity Read ↗

STAT1 Gain-of-Function and Hidradenitis Suppurativa Successfully Managed with BaricitinibSemantic proximity Read ↗

New Drug Treats Rare Genetic Overgrowth Disorder.Semantic proximity Read ↗

A Rare Cause of Hypercalcemia In Adults: Idiopathic Infantile HypercalcemiaSemantic proximity Read ↗

Cinacalcet for Symptomatic Hypercalcemia Caused by AP2S1 Mutations.Semantic proximity Read ↗

Screening for cancer in children with Costello syndrome.Semantic proximity Read ↗

Recommendations for the management of gastrointestinal comorbidities with or without trofinetide use in Rett syndromeSemantic proximity Read ↗

Baricitinib Treatment in RNU7-1-Associated Aicardi-Goutières Syndrome in a South African Child: A Case Report.Semantic proximity Read ↗

Rapamycin treatment for a child with germline PTEN mutationSemantic proximity Read ↗

[A pathogenic mutation in the COPA gene causes a family of COPA syndrome].Semantic proximity Read ↗

A Case of SLC29A3 Spectrum Disorder-Unresponsive to Multiple Immunomodulatory Therapies.Semantic proximity Read ↗

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