Human STAT1 Gain-of-Function Heterozygous Mutations: Chronic Mucocutaneous Candidiasis and Type I Interferonopathy Satoshi OkadaTakaki AsanoAnne Puel CME Review 27 August 2020 Pages: 1065 - 1081
Immune Alterations in a Patient with SARS-CoV-2-Related Acute Respiratory Distress Syndrome Lila BouadmaAurélie WiedemannYves Lévy Original Article Open access 22 August 2020 Pages: 1082 - 1092
A Nonsense N –Terminus NFKB2 Mutation Leading to Haploinsufficiency in a Patient with a Predominantly Antibody Deficiency Hye Sun KuehnAndrea BernasconiSergio D. Rosenzweig Original Article Open access 19 August 2020 Pages: 1093 - 1101
Correction to: A Nonsense N –Terminus NFKB2 Mutation Leading to Haploinsufficiency in a Patient with a Predominantly Antibody Deficiency Hye Sun KuehnAndrea BernasconiSergio D. Rosenzweig Correction 09 September 2020 Pages: 1102 - 1102
Clinical and Immunological Characterization of Combined Immunodeficiency Due to TFRC Mutation in Eight Patients Amal H. AljohaniHamoud Al-MousaBandar Al-Saud Original Article 27 August 2020 Pages: 1103 - 1110
Case Report: Acute Thrombotic Microangiopathy in a Patient with STING-Associated Vasculopathy with Onset in Infancy (SAVI) Mia MaSamia MazumderMelissa Gregory Original Article 29 August 2020 Pages: 1111 - 1115
Hematopoietic Stem Cell Transplantation in Children with Inborn Errors of Immunity: a Multi-center Experience in Colombia Manuela OlayaAlexis FrancoDiego Medina-Valencia Original Article 02 September 2020 Pages: 1116 - 1123
Adenosine Deaminase (ADA)–Deficient Severe Combined Immune Deficiency (SCID) in the US Immunodeficiency Network (USIDNet) Registry Caroline Y. KuoElizabeth GarabedianDonald B. Kohn Original Article 02 September 2020 Pages: 1124 - 1131
Helicobacter cinaedi-Associated Refractory Cellulitis in Patients with X-Linked Agammaglobulinemia Kento InoueSaeko SasakiHirokazu Kanegane Original Article 10 September 2020 Pages: 1132 - 1137
Long-Term Survival after Progressive Multifocal Leukoencephalopathy in a Patient with Primary Immune Deficiency and NFKB1 Mutation Emke MaréchalKarolien BeelBarbara Willekens Original Article 11 September 2020 Pages: 1138 - 1143
Nocardiosis Associated with Primary Immunodeficiencies (Nocar-DIP): an International Retrospective Study and Literature Review Emmanuel LafontBeatriz E. MarcianoDavid Lebeaux Original Article 12 September 2020 Pages: 1144 - 1155
Heterozygous TLR3 Mutation in Patients with Hantavirus Encephalitis Terhi PartanenJie ChenTimo Hautala Original Article Open access 16 September 2020 Pages: 1156 - 1162
Phenoidentical HLA-Related Hematopoietic Stem Cell Transplant Without Conditioning to Reconstitute a Patient with a Putative Loss-of-Function CARD11 Mutation Bashayer Al-RasheedAnas M. AlazamiHamoud Al-Mousa Letter to Editor 19 August 2020 Pages: 1163 - 1165
Disseminated Mycobacterium xenopi in an Adult with IL-12Rβ1 Deficiency Boaz PaltererFilippo BartalesiPaola Parronchi Letter to Editor 27 August 2020 Pages: 1166 - 1170
Non-Tuberculous Mycobacterial Infection in Hematopoietic Cell Transplant Anthony SabulskiStella M. DaviesSharat Chandra Letter to Editor 29 August 2020 Pages: 1171 - 1175
X-Linked Thrombocytopenia and Vanishing White Matter Disease in a Child: Double Tragedy Rakesh Kumar PilaniaGummadi AnjaniAmit Rawat Letter to Editor 31 August 2020 Pages: 1176 - 1180
Neurologic Conditions and Symptoms Reported Among Common Variable Immunodeficiency Patients in the USIDNET Michael LeeJenna NguyenIris M. Otani Letter to Editor 08 September 2020 Pages: 1181 - 1183
Refractory Autoimmune Cytopenia in a Young Boy with a Novel LRBA Mutation Successfully Managed with Sirolimus Aaqib Zaffar BandayAnkur Kumar JindalAmit Rawat Letter to Editor 10 September 2020 Pages: 1184 - 1186
DNA Ligase IV Deficiency Identified by Chance Following Vaccine-Derived Rubella Virus Infection Kazuaki MatsumotoAkihiro HoshinoTomohiro Morio Letter to Editor 10 September 2020 Pages: 1187 - 1190
Successful Hematopoietic Stem Cell Transplantation in a Patient with Complete IFN-γ Receptor 2 Deficiency: a Case Report and Literature Review Pier-Angelo TovoSilvia GarazzinoFranca Fagioli Letter to Editor Open access 10 September 2020 Pages: 1191 - 1195
A Cry for the Development of Newborn Screening for Familial Hemophagocytic Lymphohistiocytosis Akihiro HoshinoYang XiHirokazu Kanegane Letter to Editor 10 September 2020 Pages: 1196 - 1198
Spontaneous Gastrointestinal Perforations in STAT3-Deficient Hyper-IgE Syndrome Sumona BhattacharyaHastings WilliamsonAlexandra F. Freeman Letter to Editor 11 September 2020 Pages: 1199 - 1203
A Case of Burkholderia Prostatitis in a Patient with Chronic Granulomatous Disease Sameer BahalNisha VermaSiobhan O. Burns Letter to Editor 16 September 2020 Pages: 1204 - 1206
Ruxolitinib Controls Lymphoproliferation and Diabetes in a STAT3-GOF Patient Oliver WegehauptTina MuckenhauptCarsten Speckmann Letter to Editor Open access 17 September 2020 Pages: 1207 - 1210
Correction: Chronic Granulomatous Disease-Associated IBD Resolves and Does Not Adversely Impact Survival Following Allogeneic HCT Rebecca A. MarshJennifer W. Leidingsubmitted on behalf of the Primary Immune Deficiency Treatment Consortium Correction 29 August 2020 Pages: 1211 - 1213