CASE REPORT
Published on 18 Sep 2024
A case report navigating CVID and sarcoidosis overlaps in pediatric nephritis
doi 10.3389/fped.2024.1417724
- 1,227 views
- Frontiers in Pediatrics
- Pediatric Immunology
- Research Topics
- Meaningful Cases of Primary Immunodeficiencies, volume IV
Meaningful Cases of Primary Immunodeficiencies, volume IV
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Articles
CASE REPORT
Published on 20 Aug 2024
Case Report: p40phox deficiency underlying pediatric-onset systemic lupus erythematosus
doi 10.3389/fped.2024.1425874
- 876 views
CASE REPORT
Published on 16 Aug 2024
Case Report: Aplastic anemia related to a novel CTLA4 variant
doi 10.3389/fped.2024.1434076
- 1,343 views
CASE REPORT
Published on 24 Jul 2024
Case Report: C3 deficiency in two siblings
doi 10.3389/fped.2024.1424380
- 1,303 views
- 2 citations
ORIGINAL RESEARCH
Published on 23 Jul 2024
An efficient and successful outcome after haematopoietic stem cell transplantation in a patient with an LPS-responsive beige-like anchor gene mutation
doi 10.3389/fped.2024.1420118
- 781 views
CASE REPORT
Published on 28 Jun 2024
Case Report: Common variable immunodeficiency phenotype and granulomatous–lymphocytic interstitial lung disease with a novel SOCS1 variant
doi 10.3389/fped.2024.1423858
- 953 views
CASE REPORT
Published on 24 Jun 2024
Case Report: Early presentation of hereditary angioedema symptoms in a 2-year-old boy
doi 10.3389/fped.2024.1408110
- 1,291 views
CASE REPORT
Published on 07 Mar 2024
Case Report: Profound newborn leukopenia related to a novel RAC2 variant
doi 10.3389/fped.2024.1365187
- 1,840 views
- 1 citation
CASE REPORT
Published on 28 Feb 2024
A case report of a patient with recurrent and severe infections highlighting the importance of considering inborn errors of immunity
doi 10.3389/fped.2024.1340367
- 1,743 views
- 1 citation
PERSPECTIVE
Published on 23 Nov 2023
Opinion paper: effectiveness of sirolimus in treating partial Di George syndrome with autoimmune lymphoproliferative syndrome-like features
doi 10.3389/fped.2023.1242652
- 738 views
CASE REPORT
Published on 13 Jul 2023
Case report: Artemis deficiency and 3M syndrome—coexistence of two distinct genetic disorders
doi 10.3389/fped.2023.1211254
- 2,150 views
- 4 citations
