HEM1 Actin Immunodysregulatory Disorder: Genotypes, Phenotypes, and Future Directions Sarah CookMichael J. LenardoAlexandra F. Freeman CME Review Open access 22 July 2022 Pages: 1583 - 1592
Anaphylaxis to SARS-CoV-2 Vaccines in the Setting of a Nationwide Passive Epidemiological Surveillance Program Carla Toledo-SalinasSelma Cecilia Scheffler-MendozaDavid Alejandro Mendoza-Hernández Original Article 17 August 2022 Pages: 1593 - 1599
Post-SARS-CoV-2 Atypical Inflammatory Syndrome in a Toddler with X-Linked Inhibitor of Apoptosis Deficiency After Stem Cell Transplant Prasanth G. NarahariJennifer GebbiaMelissa Gans Letter to Editor 11 July 2022 Pages: 1600 - 1603
Reduced Intensity Conditioning Allogeneic Transplant for SCID Associated with Cartilage Hair Hypoplasia Taylor FitchJack BleesingSharat Chandra Letter to Editor 15 July 2022 Pages: 1604 - 1607
First Successful Allogeneic Hematopoietic Stem Cell Transplantation for MKL1 Deficiency Sanne OegemaStefanie S. V. HenrietDagmar Berghuis Letter to Editor 20 July 2022 Pages: 1608 - 1610
Chronic Enteroviral Meningoencephalitis in a Patient with Good’s Syndrome Treated with Pocapavir Alexandros GrammatikosPhilip BrightMark Gompels Letter to Editor Open access 23 July 2022 Pages: 1611 - 1613
Optical Genomic Mapping Identified a Heterozygous Structural Variant in NCF2 Related to Chronic Granulomatous Disease Xiaoying HuiJingmin YangXiaochuan Wang Letter to Editor Open access 28 July 2022 Pages: 1614 - 1617
Adenosine Deaminase (ADA) Deficiency: Report of Six New Cases and Reappraisal of Cutaneous Hypermelanosis as an Early Feature Samin SharafianGabriella JacomelliNima Parvaneh Letter to Editor 29 July 2022 Pages: 1618 - 1621
Disseminated Cryptococcosis in a Patient with CD40 Ligand Deficiency Ugo FrançoiseEmmanuel LafontOlivier Lortholary Letter to Editor 06 August 2022 Pages: 1622 - 1625
Evaluation of Laboratory and Sonographic Parameters for Detection of Portal Hypertension in Patients with Common Variable Immunodeficiency Anna-Maria GlobigValentina StrohmeierKlaus Warnatz Original Article Open access 11 July 2022 Pages: 1626 - 1637
A Novel Homozygous Stop Mutation in IL23R Causes Mendelian Susceptibility to Mycobacterial Disease Frederik StaelsFlaminia LorenzettiRik Schrijvers Original Article Open access 13 July 2022 Pages: 1638 - 1652
SLGT2 Inhibitor Rescues Myelopoiesis in G6PC3 Deficiency Prashant HiwarkarUmair BargirMukesh Desai Original Article 15 July 2022 Pages: 1653 - 1659
Algerian Registry for Inborn Errors of Immunity in Children: Report of 887 Children (1985–2021) Abdelghani YagoubiAzzeddine TahiatRachida Boukari Original Article 15 July 2022 Pages: 1660 - 1671
Novel CD81 Mutations in a Chinese Patient Led to IgA Nephropathy and Impaired BCR Signaling Lu YangPing LiuXiaodong Zhao Original Article 18 July 2022 Pages: 1672 - 1684
Novel RAB27A Variant Associated with Late-Onset Hemophagocytic Lymphohistiocytosis Alters Effector Protein Binding Timo C. E. ZondagLamberto Torralba-RagaYenan T. Bryceson Original Article Open access 23 July 2022 Pages: 1685 - 1695
TREC/KREC Newborn Screening followed by Next-Generation Sequencing for Severe Combined Immunodeficiency in Japan Manabu WakamatsuDaiei KojimaYoshiyuki Takahashi Original Article 28 July 2022 Pages: 1696 - 1707
Inborn Errors of Immunity in Patients with Adverse Events Following BCG Vaccination in Brazil Paula T. LyraEdvaldo SouzaJoão Bosco Oliveira Original Article 30 July 2022 Pages: 1708 - 1720
Clinical and Immunological Defects and Outcomes in Patients with Chromosome 22q11.2 Deletion Syndrome Hsin-Hui YuYin-Hsiu ChienBor-Luen Chiang Original Article 04 August 2022 Pages: 1721 - 1729
Cryptococcus gattii Infection as the Major Clinical Manifestation in Patients with Autoantibodies Against Granulocyte–Macrophage Colony-Stimulating Factor Shang-Yu WangYu-Fang LoCheng-Lung Ku Original Article 10 August 2022 Pages: 1730 - 1741
A Novel Assay in Whole Blood Demonstrates Restoration of Mitochondrial Activity in Phagocytes After Successful HSCT in Hyperinflamed X-Linked Chronic Granulomatous Disease Maddalena MigliavaccaLuca Basso RicciMaria Ester Bernardo Original Article Open access 10 August 2022 Pages: 1742 - 1747
Disease Progression of WHIM Syndrome in an International Cohort of 66 Pediatric and Adult Patients Christoph B. GeierMaryssa EllisonJolan E. Walter Original Article Open access 10 August 2022 Pages: 1748 - 1765
SOCS1 Haploinsufficiency Presenting as Severe Enthesitis, Bone Marrow Hypocellularity, and Refractory Thrombocytopenia in a Pediatric Patient with Subsequent Response to JAK Inhibition Thomas F. MichniackiKelly WalkovichPui Y. Lee Original Article 17 August 2022 Pages: 1766 - 1777
Genetic and Functional Identifying of Novel STAT1 Loss-of-Function Mutations in Patients with Diverse Clinical Phenotypes Xuemei ChenJunjie ChenXiaodong Zhao Original Article 17 August 2022 Pages: 1778 - 1794
High Inborn Errors of Immunity Risk in Patients with Granuloma Merve SüleymanOğuzhan SerinDeniz Çağdaş Original Article 18 August 2022 Pages: 1795 - 1809
Correction to: Peeling Skin Syndrome Type 1: Dupilumab Reduces IgE, But Not Skin Anomalies Alexis BarrancaNathalie JoncaJuliette Mazereeuw-Hautier Correction 23 July 2022 Pages: 1810 - 1810