Bourgeoning Scientific Research in Down Syndrome Dusan Bogunovic Commentary 25 July 2020 Pages: 789 - 790
Inborn Errors of Adaptive Immunity in Down Syndrome Ruud H.J. VerstegenMaaike A.A. Kusters CME Review 07 July 2020 Pages: 791 - 806
Three Copies of Four Interferon Receptor Genes Underlie a Mild Type I Interferonopathy in Down Syndrome Xiao-Fei KongLisa WorleyAnne Puel Original Article 22 June 2020 Pages: 807 - 819
Clinical Phenotypes and Immunological Characteristics of 18 Egyptian LRBA Deficiency Patients Safa MeshaalRabab El HawaryAisha Elmarsafy Original Article 06 June 2020 Pages: 820 - 832
A Case with Purine Nucleoside Phosphorylase Deficiency Suffering from Late-Onset Systemic Lupus Erythematosus and Lymphoma Bandar Al-SaudZainab Al AlawiSulaiman M. Al-Mayouf Original Article 08 June 2020 Pages: 833 - 839
Proteomic Analysis of the Acid-Insoluble Fraction of Whole Saliva from Patients Affected by Different Forms of Non-histaminergic Angioedema Davide FirinuMorena ArbaMaria T. Sanna Original Article 10 June 2020 Pages: 840 - 850
Prevalence of Immunological Defects in a Cohort of 97 Rubinstein–Taybi Syndrome Patients Francesco SaettiniRichard HerriotRaffaele Badolato Original Article 27 June 2020 Pages: 851 - 860
Treosulfan-Based Conditioning Regimen in Haematopoietic Stem Cell Transplantation with TCRαβ/CD19 Depletion in Nijmegen Breakage Syndrome. Alexandra LaberkoElvira SultanovaDmitry Balashov Original Article 30 June 2020 Pages: 861 - 871
Mendelian Susceptibility to Mycobacterial Disease (MSMD): Clinical and Genetic Features of 32 Iranian Patients Seyed Alireza MahdavianiDavood MansouriAli Akbar Velayati Original Article 30 June 2020 Pages: 872 - 882
Lymphoma Predisposing Gene in an Extended Family: CD70 Signaling Defect Khusan KhodzhaevSema Buyukkapu BayMuge Sayitoglu Original Article 03 July 2020 Pages: 883 - 892
Haploidentical Hematopoietic Stem Cell Transplantation for XIAP Deficiency: a Single-Center Report Jun YangGuang-Hua ZhuMao-Quan Qin Original Article 05 July 2020 Pages: 893 - 900
Neuroinflammatory Disease as an Isolated Manifestation of Hemophagocytic Lymphohistiocytosis Annaliesse BlincoeMaximilian HeegElie Haddad Original Article 07 July 2020 Pages: 901 - 916
Deficiency of Adenosine Deaminase 2 (DADA2): Hidden Variants, Reduced Penetrance, and Unusual Inheritance Oskar SchnappaufQing ZhouIvona Aksentijevich Original Article 08 July 2020 Pages: 917 - 926
A 23-Year Follow-Up of a Patient with Gain-of-Function IkB-Alpha Mutation and Stable Full Chimerism After Hematopoietic Stem Cell Transplantation Francesca ContiRita CarsettiCaterina Cancrini Letter to Editor 02 July 2020 Pages: 927 - 933
Poikiloderma with Neutropenia, Clericuzio-Type Accompanied by Loss of Digits Due to Severe Osteomyelitis Neslihan AkdoganErdem KindisSibel Ersoy-Evans Letter to Editor 04 July 2020 Pages: 934 - 939
Ocular Manifestations of Chronic Granulomatous Disease: First Report of Coats’ Disease and Literature Review Mahsima ShabaniRoxana PazoukiNima Parvaneh Letter to Editor 07 July 2020 Pages: 940 - 947
Late-Onset EBV Susceptibility and Refractory Pure Red Cell Aplasia Revealing DADA2 Tom Le VoyerDavid BoutboulGuillaume Le Guenno Letter to Editor 08 July 2020 Pages: 948 - 953