Found: 16
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A Novel FOXN1 Variant Is Identified in Two Siblings with Nude Severe Combined Immunodeficiency.
- Published in:
- 2019
- By:
- Publication type:
- Letter
Nasal Nitric Oxide in Primary Immunodeficiency and Primary Ciliary Dyskinesia: Helping to Distinguish Between Clinically Similar Diseases.
- Published in:
- Journal of Clinical Immunology, 2019, v. 39, n. 2, p. 216, doi. 10.1007/s10875-019-00613-8
- By:
- Publication type:
- Article
Immune Dysregulation and Disease Pathogenesis due to Activating Mutations in PIK3CD—the Goldilocks' Effect.
- Published in:
- Journal of Clinical Immunology, 2019, v. 39, n. 2, p. 148, doi. 10.1007/s10875-019-00612-9
- By:
- Publication type:
- Article
Correction to: Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group.
- Published in:
- 2019
- By:
- Publication type:
- Correction Notice
Severe Transitory Neonatal Neutropenia Associated with Maternal Autoimmune or Idiopathic Neutropenia.
- Published in:
- Journal of Clinical Immunology, 2019, v. 39, n. 2, p. 200, doi. 10.1007/s10875-019-00608-5
- By:
- Publication type:
- Article
Health-Related Quality of Life and Emotional Health in X-Linked Carriers of Chronic Granulomatous Disease in the United Kingdom.
- Published in:
- Journal of Clinical Immunology, 2019, v. 39, n. 2, p. 195, doi. 10.1007/s10875-019-00607-6
- By:
- Publication type:
- Article
Alternative Splicing Rescues Loss of Common Gamma Chain Function and Results in IL-21R-like Deficiency.
- Published in:
- Journal of Clinical Immunology, 2019, v. 39, n. 2, p. 207, doi. 10.1007/s10875-019-00606-7
- By:
- Publication type:
- Article
In Memoriam: Fernando Aiuti, MD (June 8, 1935–January 9, 2019).
- Published in:
- 2019
- By:
- Publication type:
- Letter
Novel Heterogeneous Mutation of TNFAIP3 in a Chinese Patient with Behçet-Like Phenotype and Persistent EBV Viremia.
- Published in:
- Journal of Clinical Immunology, 2019, v. 39, n. 2, p. 188, doi. 10.1007/s10875-019-00604-9
- By:
- Publication type:
- Article
IFN-g:IL-10 Ratio: a Putative Predictive Biomarker to Discriminate HLH From Severe Viral Infections.
- Published in:
- 2019
- By:
- Publication type:
- Letter
Haploidentical Stem Cell Transplantation with Post-Transplant Cyclophosphamide for Primary Immune Deficiency Disorders in Children: Challenges and Outcome from a Tertiary Care Center in South India.
- Published in:
- Journal of Clinical Immunology, 2019, v. 39, n. 2, p. 182, doi. 10.1007/s10875-019-00600-z
- By:
- Publication type:
- Article
Auto-inflammation in a Patient with a Novel Homozygous OTULIN Mutation.
- Published in:
- 2019
- By:
- Publication type:
- Letter
Compound Heterozygous Mutations of IL2-Inducible T cell Kinase in a Swedish Patient: the Importance of Early Genetic Diagnosis.
- Published in:
- 2019
- By:
- Publication type:
- Letter
A Novel Recessive Mutation of Interferon-γ Receptor 1 in a Patient with Mycobacterium tuberculosis in Bone Marrow Aspirate.
- Published in:
- 2019
- By:
- Publication type:
- Letter
Neurological Involvement in Childhood Evans Syndrome.
- Published in:
- Journal of Clinical Immunology, 2019, v. 39, n. 2, p. 171, doi. 10.1007/s10875-019-0594-3
- By:
- Publication type:
- Article
Health-Related Quality of Life in Patients with CVID Under Different Schedules of Immunoglobulin Administration: Prospective Multicenter Study.
- Published in:
- Journal of Clinical Immunology, 2019, v. 39, n. 2, p. 159, doi. 10.1007/s10875-019-0592-5
- By:
- Publication type:
- Article