Works matching IS 02719142 AND DT 2022 AND VI 42 AND IP 5
Results: 20
Intravenous Immunoglobulins Promote an Expansion of Monocytic Myeloid-Derived Suppressor Cells (MDSC) in CVID Patients.
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- Journal of Clinical Immunology, 2022, v. 42, n. 5, p. 1093, doi. 10.1007/s10875-022-01277-7
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- Article
Copy Number Analysis in a Large Cohort Suggestive of Inborn Errors of Immunity Indicates a Wide Spectrum of Relevant Chromosomal Losses and Gains.
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- Journal of Clinical Immunology, 2022, v. 42, n. 5, p. 1083, doi. 10.1007/s10875-022-01276-8
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- Article
Genetic Testing in Egyptian Patients with Inborn Errors of Immunity: a Single-Center Experience.
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- Journal of Clinical Immunology, 2022, v. 42, n. 5, p. 1051, doi. 10.1007/s10875-022-01272-y
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- Article
Common Variable Immunodeficiency in a Carrier of the ADA2 R169Q Variant: Coincidence or Causality?
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- Journal of Clinical Immunology, 2022, v. 42, n. 5, p. 959, doi. 10.1007/s10875-022-01271-z
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- Article
Candidalysin, a Virulence Factor of Candida albicans, Stimulates Mast Cells by Mediating Cross-Talk Between Signaling Pathways Activated by the Dectin-1 Receptor and MAPKs.
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- Journal of Clinical Immunology, 2022, v. 42, n. 5, p. 1009, doi. 10.1007/s10875-022-01267-9
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EPG5 Compound Heterozygous Unreported Pathogenic Variants in a Mexican Patient with Vici Syndrome.
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- Journal of Clinical Immunology, 2022, v. 42, n. 5, p. 952, doi. 10.1007/s10875-022-01266-w
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PAMI Syndrome: Two Cases of an Autoinflammatory Disease with an ALPS-Like Phenotype.
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- Journal of Clinical Immunology, 2022, v. 42, n. 5, p. 955, doi. 10.1007/s10875-022-01265-x
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A High-Throughput Amplicon Screen for Somatic UBA1 Variants in Cytopenic and Giant Cell Arteritis Cohorts.
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- Journal of Clinical Immunology, 2022, v. 42, n. 5, p. 947, doi. 10.1007/s10875-022-01258-w
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Development of Laboratory Parameters-Based Formulas in Predicting Short Outcomes for Adult Hemophagocytic Lymphohistiocytosis Patients with Different Underlying Diseases.
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- Journal of Clinical Immunology, 2022, v. 42, n. 5, p. 1000, doi. 10.1007/s10875-022-01263-z
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Clinical and Laboratory Factors Affecting the Prognosis of Severe Combined Immunodeficiency.
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- Journal of Clinical Immunology, 2022, v. 42, n. 5, p. 1036, doi. 10.1007/s10875-022-01262-0
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Granulocyte Transfusions in Patients with Chronic Granulomatous Disease Undergoing Hematopoietic Cell Transplantation or Gene Therapy.
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- Journal of Clinical Immunology, 2022, v. 42, n. 5, p. 1026, doi. 10.1007/s10875-022-01261-1
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- Article
Correction to: Dexamethasone Treatment for COVID-19-Related Lung Injury in an Adult with WHIM Syndrome.
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- Journal of Clinical Immunology, 2022, v. 42, n. 5, p. 1106, doi. 10.1007/s10875-022-01260-2
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- Article
The Impact of SARS-CoV-2 Infection in Patients with Inborn Errors of Immunity: the Experience of the Italian Primary Immunodeficiencies Network (IPINet).
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- Journal of Clinical Immunology, 2022, v. 42, n. 5, p. 935, doi. 10.1007/s10875-022-01264-y
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- Article
Impact of JAK Inhibitors in Pediatric Patients with STAT1 Gain of Function (GOF) Mutations—10 Children and Review of the Literature.
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- Journal of Clinical Immunology, 2022, v. 42, n. 5, p. 1071, doi. 10.1007/s10875-022-01257-x
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SARS-CoV-2-Specific and Functional Cytotoxic CD8 Cells in Primary Antibody Deficiency: Natural Infection and Response to Vaccine.
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- Journal of Clinical Immunology, 2022, v. 42, n. 5, p. 914, doi. 10.1007/s10875-022-01256-y
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- Article
Responses to SARS-CoV-2 Vaccines of Patients with Common Variable Immune Deficiencies and X-linked Agammaglobulinemia.
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- Journal of Clinical Immunology, 2022, v. 42, n. 5, p. 911, doi. 10.1007/s10875-022-01251-3
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Pulmonary Alveolar Proteinosis and Multiple Infectious Diseases in a Child with Autosomal Recessive Complete IRF8 Deficiency.
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- Journal of Clinical Immunology, 2022, v. 42, n. 5, p. 975, doi. 10.1007/s10875-022-01250-4
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SARS-CoV-2 Vaccine Responses in Individuals with Antibody Deficiency: Findings from the COV-AD Study.
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- Journal of Clinical Immunology, 2022, v. 42, n. 5, p. 923, doi. 10.1007/s10875-022-01231-7
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Interpretation of Dihydrorhodamine-1,2,3 Flow Cytometry in Chronic Granulomatous Disease: an Atypical Exemplar.
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- Journal of Clinical Immunology, 2022, v. 42, n. 5, p. 986, doi. 10.1007/s10875-022-01217-5
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Mutations in RNU7-1 Weaken Secondary RNA Structure, Induce MCP-1 and CXCL10 in CSF, and Result in Aicardi-Goutières Syndrome with Severe End-Organ Involvement.
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- Journal of Clinical Immunology, 2022, v. 42, n. 5, p. 962, doi. 10.1007/s10875-022-01209-5
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