Works matching IS 02719142 AND DT 2022 AND VI 42 AND IP 4
Results: 35
Atypical Autosomal Recessive AID Deficiency—Yet Another Piece of the Hyper-IgM Puzzle.
- Published in:
- 2022
- By:
- Publication type:
- Editorial
Prevalence of APECED-Like Clinical Disease in an Electronic Health Record Database, USA.
- Published in:
- 2022
- By:
- Publication type:
- Letter
Oral Ulcers Resolution Using IL12/23 Blockade in an Infant with Leukocyte Adhesion Deficiency Type 1.
- Published in:
- 2022
- By:
- Publication type:
- Letter
PEPD-Related Prolidase Deficiency Presenting as Hyper-immunoglobulin E Syndrome.
- Published in:
- 2022
- By:
- Publication type:
- Letter
Recurrent Breast Abscesses in a Female with Autosomal Dominant Hyper-IgE Syndrome.
- Published in:
- 2022
- By:
- Publication type:
- Letter
Lung MRI- Changing Paradigms in Evaluation of Chronic Granulomatous Disease in Children.
- Published in:
- 2022
- By:
- Publication type:
- Letter
22q11.2 Deletion and Duplication Syndromes and COVID-19.
- Published in:
- 2022
- By:
- Publication type:
- Letter
Diagnosis of APS-1 in Two Siblings Following Life-Threatening COVID-19 Pneumonia.
- Published in:
- 2022
- By:
- Publication type:
- Letter
Elevated CD21<sup>low</sup> B Cell Frequency Is a Marker of Poor Immunity to Pfizer-BioNTech BNT162b2 mRNA Vaccine Against SARS-CoV-2 in Patients with Common Variable Immunodeficiency.
- Published in:
- Journal of Clinical Immunology, 2022, v. 42, n. 4, p. 716, doi. 10.1007/s10875-022-01244-2
- By:
- Publication type:
- Article
Loss of Function Mutation in ELF4 Causes Autoinflammatory and Immunodeficiency Disease in Human.
- Published in:
- Journal of Clinical Immunology, 2022, v. 42, n. 4, p. 798, doi. 10.1007/s10875-022-01243-3
- By:
- Publication type:
- Article
Correction to: Fatal and Unresponsive Cytomegalovirus Infection in a New Homozygous FOXN1 Gene Variation Causing Nude SCID.
- Published in:
- 2022
- By:
- Publication type:
- Correction Notice
Low Lymphocytes and IFN-Neutralizing Autoantibodies as Biomarkers of COVID-19 Mortality.
- Published in:
- 2022
- By:
- Publication type:
- Letter
A Novel Kindred with MyD88 Deficiency.
- Published in:
- 2022
- By:
- Publication type:
- Letter
TCRαβ-Depleted Haploidentical Grafts Are a Safe Alternative to HLA-Matched Unrelated Donor Stem Cell Transplants for Infants with Severe Combined Immunodeficiency.
- Published in:
- Journal of Clinical Immunology, 2022, v. 42, n. 4, p. 851, doi. 10.1007/s10875-022-01239-z
- By:
- Publication type:
- Article
Hematopoietic Cell Transplantation for Adenosine Deaminase Severe Combined Immunodeficiency—Improved Outcomes in the Modern Era.
- Published in:
- Journal of Clinical Immunology, 2022, v. 42, n. 4, p. 819, doi. 10.1007/s10875-022-01238-0
- By:
- Publication type:
- Article
X-Linked Agammaglobulinemia: Infection Frequency and Infection-Related Mortality in the USIDNET Registry.
- Published in:
- Journal of Clinical Immunology, 2022, v. 42, n. 4, p. 827, doi. 10.1007/s10875-022-01237-1
- By:
- Publication type:
- Article
A Case of XIAP Deficiency Successfully Managed with Tadekinig Alfa (rhIL-18BP).
- Published in:
- 2022
- By:
- Publication type:
- Letter
Transient Increase of Pre-existing Anti-IFN-α2 Antibodies Induced by SARS-CoV-2 Infection.
- Published in:
- 2022
- By:
- Publication type:
- Letter
Progressive Depletion of B and T Lymphocytes in Patients with Ataxia Telangiectasia: Results of the Italian Primary Immunodeficiency Network.
- Published in:
- Journal of Clinical Immunology, 2022, v. 42, n. 4, p. 783, doi. 10.1007/s10875-022-01234-4
- By:
- Publication type:
- Article
A Novel AICDA Splice-Site Mutation in Two Siblings with HIGM2 Permits Somatic Hypermutation but Abrogates Mutational Targeting.
- Published in:
- Journal of Clinical Immunology, 2022, v. 42, n. 4, p. 771, doi. 10.1007/s10875-022-01233-5
- By:
- Publication type:
- Article
STAT 3 GOF with Polycythemia: a Twist to the Tale-First Case Report from India.
- Published in:
- 2022
- By:
- Publication type:
- Letter
Pneumococcal IgG Antibody Responses to 23vPPV in Healthy Controls Using an Automated ELISA.
- Published in:
- Journal of Clinical Immunology, 2022, v. 42, n. 4, p. 760, doi. 10.1007/s10875-022-01230-8
- By:
- Publication type:
- Article
Inborn Errors of Immunity in Latvia: Analysis of Data from 1994 to 2020.
- Published in:
- 2022
- By:
- Publication type:
- Letter
First Identified Case of Fatal Fulminant Eosinophilic Myocarditis Following the Initial Dose of the Pfizer-BioNTech mRNA COVID-19 Vaccine (BNT162b2, Comirnaty): an Extremely Rare Idiosyncratic Necrotizing Hypersensitivity Reaction Different to Hypersensitivity or Drug-Induced Myocarditis
- Published in:
- 2022
- By:
- Publication type:
- Letter
Fatal JC-virus Granular Cerebellar Neuronopathy in a Patient Diagnosed with ALPS and Hypogammaglobulinemia.
- Published in:
- 2022
- By:
- Publication type:
- Letter
A Case Report of Fatal Mucormycosis in a 30-Year-Old Patient with Autoimmune Polyendocrine Syndrome Type 1.
- Published in:
- 2022
- By:
- Publication type:
- Letter
Post-SARS-CoV-2 Vaccine Monitoring of Disease Flares in Autoinflammatory Diseases.
- Published in:
- 2022
- By:
- Publication type:
- Letter
Lymphocytes Utilize Somatic Mutations, Epigenetic Silencing, and the Proteasome to Escape Truncated WASP Expression.
- Published in:
- Journal of Clinical Immunology, 2022, v. 42, n. 4, p. 753, doi. 10.1007/s10875-022-01224-6
- By:
- Publication type:
- Article
COVID-19 Vaccine Uptake and Efficacy in a National Immunodeficiency Cohort.
- Published in:
- 2022
- By:
- Publication type:
- Letter
Health-Related Quality of Life in 91 Patients with X-Linked Agammaglobulinemia.
- Published in:
- Journal of Clinical Immunology, 2022, v. 42, n. 4, p. 811, doi. 10.1007/s10875-022-01222-8
- By:
- Publication type:
- Article
Activated Phosphoinositide 3-Kinase δ Syndrome: a Large Pediatric Cohort from a Single Center in China.
- Published in:
- Journal of Clinical Immunology, 2022, v. 42, n. 4, p. 837, doi. 10.1007/s10875-022-01218-4
- By:
- Publication type:
- Article
Early Onset of TNFα-Driven Arthritis, Auto-inflammation, and Progressive Loss of Vision in a Patient with ALPK1 Mutation.
- Published in:
- 2022
- By:
- Publication type:
- Letter
Correction to: Hemophagocytic lymphohistiocytosis in activated PI3K delta syndrome, an illustrative case report.
- Published in:
- 2022
- By:
- Publication type:
- Correction Notice
Peeling Skin Syndrome Type 1: Dupilumab Reduces IgE, But Not Skin Anomalies.
- Published in:
- 2022
- By:
- Publication type:
- Letter
Fatal and Unresponsive Cytomegalovirus Infection in a New Homozygous FOXN1 Gene Variation Causing Nude SCID.
- Published in:
- 2022
- By:
- Publication type:
- Letter