Works matching IS 02719142 AND DT 2022 AND VI 42 AND IP 7
Results: 26
Decoding the Human Genetic and Immunological Basis of COVID-19 mRNA Vaccine-Induced Myocarditis.
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- Journal of Clinical Immunology, 2022, v. 42, n. 7, p. 1354, doi. 10.1007/s10875-022-01372-9
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- Article
Correction to: Chronic Granulomatous Disease: an Updated Experience, with Emphasis on Newly Recognized Features.
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- Journal of Clinical Immunology, 2022, v. 42, n. 7, p. 1420, doi. 10.1007/s10875-022-01370-x
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- Article
Myocarditis in 13-Year-Old Monochorionic Diamniotic Twins After COVID-19 Vaccination.
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- Journal of Clinical Immunology, 2022, v. 42, n. 7, p. 1351, doi. 10.1007/s10875-022-01360-z
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- Article
The 2022 Update of IUIS Phenotypical Classification for Human Inborn Errors of Immunity.
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- Journal of Clinical Immunology, 2022, v. 42, n. 7, p. 1508, doi. 10.1007/s10875-022-01352-z
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- Article
Correction to: Hematopoietic Stem Cell Transplantation in late-onset X-linked Chronic Granulomatous Disease in a female carrier.
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- Journal of Clinical Immunology, 2022, v. 42, n. 7, p. 1400, doi. 10.1007/s10875-022-01334-1
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- Article
Deficiency of Adenosine Deaminase 2 Presenting as Periodic Fever at the Mainland of Familial Mediterranean Fever.
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- Journal of Clinical Immunology, 2022, v. 42, n. 7, p. 1409, doi. 10.1007/s10875-022-01328-z
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- Article
Circulating Innate Lymphoid Cells (ILCs) in Healthy Children: Reference Values for Evaluation of Treatment in Immunocompromised Pediatric Patients.
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- Journal of Clinical Immunology, 2022, v. 42, n. 7, p. 1405, doi. 10.1007/s10875-022-01326-1
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- Article
Clinical and Immunological Features of SARS-CoV-2 Breakthrough Infections in Vaccinated Individuals Requiring Hospitalization.
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- Journal of Clinical Immunology, 2022, v. 42, n. 7, p. 1379, doi. 10.1007/s10875-022-01325-2
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- Article
Variant Type X91<sup>+</sup> Chronic Granulomatous Disease: Clinical and Molecular Characterization in a Chinese Cohort.
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- Journal of Clinical Immunology, 2022, v. 42, n. 7, p. 1564, doi. 10.1007/s10875-022-01324-3
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- Article
Correction to: Characterization of Novel Pathogenic Variants Leading to Caspase-8 Cleavage-Resistant RIPK1-Induced Autoinflammatory Syndrome.
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- 2022
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- Correction Notice
Raised Serum Markers of T Cell Activation and Exhaustion in Granulomatous-Lymphocytic Interstitial Lung Disease in Common Variable Immunodeficiency.
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- Journal of Clinical Immunology, 2022, v. 42, n. 7, p. 1553, doi. 10.1007/s10875-022-01318-1
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- Article
Neutralizing Type I Interferon Autoantibodies in Japanese Patients with Severe COVID-19.
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- Journal of Clinical Immunology, 2022, v. 42, n. 7, p. 1360, doi. 10.1007/s10875-022-01308-3
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- Article
Immunologic Control of Disseminated Aichi Virus Infection in X-Linked Agammaglobulinemia by Transplantation of TcRαβ-Depleted Haploidentical Hematopoietic Cells.
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- Journal of Clinical Immunology, 2022, v. 42, n. 7, p. 1401, doi. 10.1007/s10875-022-01314-5
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- Article
Long-term SARS-CoV-2 Asymptomatic Carriage in an Immunocompromised Host: Clinical, Immunological, and Virological Implications.
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- Journal of Clinical Immunology, 2022, v. 42, n. 7, p. 1371, doi. 10.1007/s10875-022-01313-6
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- Article
B-Cell Immune Reconstitution with Mixed Chimerism After Hematopoietic Cell Transplantation in a Patient with Severe Combined Immunodeficiency.
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- Journal of Clinical Immunology, 2022, v. 42, n. 7, p. 1392, doi. 10.1007/s10875-022-01311-8
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- Article
Hematopoietic Stem Cell Transplantation in Late-onset X-linked Chronic Granulomatous Disease in a Female Carrier.
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- Journal of Clinical Immunology, 2022, v. 42, n. 7, p. 1396, doi. 10.1007/s10875-022-01310-9
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- Publication type:
- Article
Risk Factors of Pneumonia in Primary Antibody Deficiency Patients Receiving Immunoglobulin Therapy: Data from the US Immunodeficiency Network (USIDNET).
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- Journal of Clinical Immunology, 2022, v. 42, n. 7, p. 1545, doi. 10.1007/s10875-022-01317-2
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- Article
Hematopoietic Stem Cell Transplantation in ARPC1B Deficiency.
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- Journal of Clinical Immunology, 2022, v. 42, n. 7, p. 1535, doi. 10.1007/s10875-022-01305-6
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- Article
Human Inborn Errors of Immunity: 2022 Update on the Classification from the International Union of Immunological Societies Expert Committee.
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- Journal of Clinical Immunology, 2022, v. 42, n. 7, p. 1473, doi. 10.1007/s10875-022-01289-3
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- Article
Patients with Chromosome 11q Deletions Are Characterized by Inborn Errors of Immunity Involving both B and T Lymphocytes.
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- Journal of Clinical Immunology, 2022, v. 42, n. 7, p. 1521, doi. 10.1007/s10875-022-01303-8
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- Article
Protein-losing Enteropathy as a Complication and/or Differential Diagnosis of Common Variable Immunodeficiency.
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- Journal of Clinical Immunology, 2022, v. 42, n. 7, p. 1461, doi. 10.1007/s10875-022-01299-1
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- Publication type:
- Article
Characterization of Novel Pathogenic Variants Leading to Caspase-8 Cleavage-Resistant RIPK1-Induced Autoinflammatory Syndrome.
- Published in:
- Journal of Clinical Immunology, 2022, v. 42, n. 7, p. 1421, doi. 10.1007/s10875-022-01298-2
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- Publication type:
- Article
Chronic Granulomatous Disease: an Updated Experience, with Emphasis on Newly Recognized Features.
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- Journal of Clinical Immunology, 2022, v. 42, n. 7, p. 1411, doi. 10.1007/s10875-022-01294-6
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- Article
A Novel CEBPE Variant Causes Severe Infections and Profound Neutropenia.
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- Journal of Clinical Immunology, 2022, v. 42, n. 7, p. 1434, doi. 10.1007/s10875-022-01304-7
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- Article
Quality of Life and Social and Psychological Outcomes in Adulthood Following Allogeneic HSCT in Childhood for Inborn Errors of Immunity.
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- Journal of Clinical Immunology, 2022, v. 42, n. 7, p. 1451, doi. 10.1007/s10875-022-01286-6
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- Article
Correction to: Hematopoietic Cell Transplantation Cures Adenosine Deaminase 2 Deficiency: Report on 30 Patients.
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- Journal of Clinical Immunology, 2022, v. 42, n. 7, p. 1580, doi. 10.1007/s10875-022-01280-y
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- Article