EDITORIAL
Published on 19 Feb 2025
Editorial: Community series in primary immunodeficiencies worldwide, volume II
doi 10.3389/fimmu.2025.1564959
- Frontiers in Immunology
- Primary Immunodeficiencies
- Research Topics
- Community Series in Primary Immunodeficiencies Worldwide, volume II
Community Series in Primary Immunodeficiencies Worldwide, volume II
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Articles
CASE REPORT
Published on 10 Dec 2024
Case report: Identification of a Chinese patient with RAG1 mutations initially presenting as autoimmune hemolytic anemia
doi 10.3389/fimmu.2024.1498066
- 597 views
CASE REPORT
Published on 20 Nov 2024
Perspectives in newborn screening for SCID in Japan. Case report: newborn screening identified X-linked severe combined immunodeficiency with a novel IL2RG variant
doi 10.3389/fimmu.2024.1478411
- 768 views
ORIGINAL RESEARCH
Published on 23 Oct 2024
Calculated globulin can be used as a screening test for antibody deficiency in children and adolescents
doi 10.3389/fimmu.2024.1495564
- 588 views
REVIEW
Published on 08 Aug 2024
X-linked severe combined immunodeficiency complicated by disseminated bacillus Calmette-Guérin disease caused by a novel pathogenic mutation in exon 3 of the IL2RG gene: a case report and literature review
doi 10.3389/fimmu.2024.1453046
- 1,540 views
- 1 citation
ORIGINAL RESEARCH
Published on 06 Aug 2024
Immune profiling and functional analysis of NK and T cells in ataxia telangiectasia
doi 10.3389/fimmu.2024.1377955
- 1,116 views
CASE REPORT
Published on 24 Jul 2024
Retrospective identification of the first cord blood–transplanted severe aplastic anemia in a STAT1-associated chronic mucocutaneous candidiasis family: case report, review of literature and pathophysiologic background
doi 10.3389/fimmu.2024.1430938
- 1,347 views
ORIGINAL RESEARCH
Published on 12 Jul 2024
Flow cytometry-based diagnostic approach for inborn errors of immunity: experience from Algeria
doi 10.3389/fimmu.2024.1402038
- 2,324 views
- 1 citation
ORIGINAL RESEARCH
Published on 28 Jun 2024
Nijmegen breakage syndrome: 25-year experience of diagnosis and treatment in Ukraine
doi 10.3389/fimmu.2024.1428724
- 1,248 views
CASE REPORT
Published on 01 Feb 2024
A unique STK4 mutation truncating only the C-terminal SARAH domain results in a mild clinical phenotype despite severe T cell lymphopenia: Case report
doi 10.3389/fimmu.2024.1329610
- 1,184 views
- 1 citation
CASE REPORT
Published on 12 Sep 2023
Case report: IKZF1-related early-onset CID is expected to be missed in TREC-based SCID screening but can be identified by determination of KREC levels
doi 10.3389/fimmu.2023.1257581
- 1,378 views
- 1 citation
Published in
Frontiers in Immunology
- Primary Immunodeficiencies
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