CASE REPORT
Published on 24 Oct 2019
Vasculitis in a Child With the Hyper-IgM Variant of Ataxia-Telangiectasia
doi 10.3389/fped.2019.00390
- 4,165 views
- 8 citations
- Frontiers in Pediatrics
- Pediatric Immunology
- Research Topics
- Meaningful Cases of Primary Immunodeficiencies: Volume 2
Meaningful Cases of Primary Immunodeficiencies: Volume 2
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Articles
CASE REPORT
Published on 15 Oct 2019
Rare TACI Mutation in a 3-Year-Old Boy With CVID Phenotype
doi 10.3389/fped.2019.00418
- 3,699 views
- 2 citations
CASE REPORT
Published on 30 Jul 2019
Novel Heterozygous Mutation in NFKB2 Is Associated With Early Onset CVID and a Functional Defect in NK Cells Complicated by Disseminated CMV Infection and Severe Nephrotic Syndrome
doi 10.3389/fped.2019.00303
- 4,333 views
- 24 citations
CASE REPORT
Published on 05 Jul 2019
Arthritis in Two Patients With Partial Recombination Activating Gene Deficiency
doi 10.3389/fped.2019.00235
- 2,229 views
- 8 citations
CASE REPORT
Published on 14 May 2019
Hematopoietic Stem Cell Transplant for the Treatment of X-MAID
doi 10.3389/fped.2019.00170
- 3,210 views
- 13 citations
CASE REPORT
Published on 30 Apr 2019
Gain-of-Function STAT1 Mutation With Familial Lymphadenopathy and Hodgkin Lymphoma
doi 10.3389/fped.2019.00160
- 3,103 views
- 10 citations
CASE REPORT
Published on 24 Apr 2019
Familial Immune Thrombocytopenia Associated With a Novel Variant in IKZF1
doi 10.3389/fped.2019.00139
- 2,361 views
- 17 citations
CASE REPORT
Published on 24 Apr 2019
A Novel STAT3 Mutation in a Qatari Patient With Hyper-IgE Syndrome
doi 10.3389/fped.2019.00130
- 3,174 views
- 7 citations
CASE REPORT
Published on 16 Apr 2019
Combined Immunodeficiency With Late-Onset Progressive Hypogammaglobulinemia and Normal B Cell Count in a Patient With RAG2 Deficiency
doi 10.3389/fped.2019.00122
- 3,580 views
- 10 citations
CASE REPORT
Published on 05 Apr 2019
Two Unique Cases of X-linked SCID: A Diagnostic Challenge in the Era of Newborn Screening
doi 10.3389/fped.2019.00055
- 7,151 views
- 12 citations
CASE REPORT
Published on 29 Mar 2019
Treatment-Responsive Granulomatous-Lymphocytic Interstitial Lung Disease in a Pediatric Case of Common Variable Immunodeficiency
doi 10.3389/fped.2019.00105
- 5,426 views
- 12 citations
CASE REPORT
Published on 28 Mar 2019
A Novel Mutation in Chronic Granulomatous Disease: Treating the Family, Not Just the Patient
doi 10.3389/fped.2019.00107
- 3,327 views
- 3 citations
Published in
Frontiers in Pediatrics
- Pediatric Immunology
Impact
- 78kTopic views
- 59kArticle views
- 17kArticle downloads