Found: 22
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Complete IFN-γR1 Deficiency in a Boy Due to UPD(6)mat with IFNGR1 Novel Splicing Variant.
- Published in:
- 2021
- By:
- Publication type:
- Letter
The First Case of BENTA Disease (B Cell Expansion with NF-κB and T Cell Anergy) from Iran.
- Published in:
- 2021
- By:
- Publication type:
- Letter
Correction to: Helicobacter cinaedi-Associated Refractory Cellulitis in Patients with X-Linked Agammaglobulinemia.
- Published in:
- 2021
- By:
- Publication type:
- Correction Notice
Genetic Mosaicism as a Cause of Inborn Errors of Immunity.
- Published in:
- Journal of Clinical Immunology, 2021, v. 41, n. 4, p. 718, doi. 10.1007/s10875-021-01037-z
- By:
- Publication type:
- Article
Correction to: Clinical and Immunological Heterogeneity in Japanese Patients with Gain-of-Function Variants in STAT3.
- Published in:
- 2021
- By:
- Publication type:
- Correction Notice
Personalized IgG Replacement Therapy for Patients with B cell Inborn Errors of Immunity.
- Published in:
- 2021
- By:
- Publication type:
- Editorial
Novel ADA2 Compound Heterozygous Mutations Resulting in Deficiency of Adenosine Deaminase 2 in a Pair of Siblings.
- Published in:
- 2021
- By:
- Publication type:
- Letter
Toxoplasmosis-Associated Hemophagocytic Lymphohistiocytosis in Allogeneic Transplantation.
- Published in:
- 2021
- By:
- Publication type:
- Letter
Clinical and Immunological Heterogeneity in Japanese Patients with Gain-of-Function Variants in STAT3.
- Published in:
- Journal of Clinical Immunology, 2021, v. 41, n. 4, p. 780, doi. 10.1007/s10875-021-00975-y
- By:
- Publication type:
- Article
C1 Esterase Inhibition: Targeting Multiple Systems in COVID-19.
- Published in:
- 2021
- By:
- Publication type:
- Letter
Infectious Complications Predict Premature CD8+ T-cell Senescence in CD40 Ligand-Deficient Patients.
- Published in:
- Journal of Clinical Immunology, 2021, v. 41, n. 4, p. 795, doi. 10.1007/s10875-021-00968-x
- By:
- Publication type:
- Article
Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations.
- Published in:
- Journal of Clinical Immunology, 2021, v. 41, n. 4, p. 756, doi. 10.1007/s10875-021-00967-y
- By:
- Publication type:
- Article
Inherited TOP2B Mutation: Possible Confirmation of Mutational Hotspots in the TOPRIM Domain.
- Published in:
- 2021
- By:
- Publication type:
- Letter
X-Linked Agammaglobulinemia Case with TH Domain Missense Mutation in Bruton Tyrosine Kinase.
- Published in:
- 2021
- By:
- Publication type:
- Letter
The Impact of the SARS-CoV-2 Pandemic in PID Patients Receiving Ig Replacement Therapy.
- Published in:
- 2021
- By:
- Publication type:
- Letter
Failure of Viral-Specific T Cells Administered in Pre-transplant Settings in Children with Inborn Errors of Immunity.
- Published in:
- Journal of Clinical Immunology, 2021, v. 41, n. 4, p. 748, doi. 10.1007/s10875-020-00961-w
- By:
- Publication type:
- Article
Successful Haploidentical Transplant Using Post-Transplant Cyclophosphamide in a Child with Chronic Granulomatous Disease—First Report from the Indian Subcontinent.
- Published in:
- 2021
- By:
- Publication type:
- Letter
Cytokine Profiles Before and After Immune Modulation in Hospitalized Patients with COVID-19.
- Published in:
- Journal of Clinical Immunology, 2021, v. 41, n. 4, p. 738, doi. 10.1007/s10875-020-00949-6
- By:
- Publication type:
- Article
Stepwise Reversal of Immune Dysregulation Due to STAT1 Gain-of-Function Mutation Following Ruxolitinib Bridge Therapy and Transplantation.
- Published in:
- Journal of Clinical Immunology, 2021, v. 41, n. 4, p. 769, doi. 10.1007/s10875-020-00943-y
- By:
- Publication type:
- Article
Aspergillus fumigatus Skull Bone Osteomyelitis and Native Valve Endocarditis in a Young Boy: an Unusual Presentation of Chronic Granulomatous Disease.
- Published in:
- 2021
- By:
- Publication type:
- Letter
Generalized Pustular Psoriasis in Patients with Interferon Gamma (IFN-γ) Receptor Deficiency and Mycobacterial Infection.
- Published in:
- 2021
- By:
- Publication type:
- Letter
Life-Saving, Dose-Adjusted, Targeted Therapy in a Patient with a STAT3 Gain-of-Function Mutation.
- Published in:
- 2021
- By:
- Publication type:
- Letter