The Growing Spectrum of Human Diseases Caused by InheritedCDC42 Mutations Helen C. SuJordan S. Orange Commentary 16 May 2020 Pages: 551 - 553
Infantile Myelofibrosis and Myeloproliferation with CDC42 Dysfunction Jeffrey M. VerboonDilnar MahmutVijay G. Sankaran Original Article Open access 17 April 2020 Pages: 554 - 566
Systemic Inflammation and Myelofibrosis in a Patient with Takenouchi-Kosaki Syndrome due to CDC42 Tyr64Cys Mutation Giorgia BucciolBethany PillayIsabelle Meyts Letter to Editor 18 January 2020 Pages: 567 - 570
A New Patient with NOCARH Syndrome Due to CDC42 Defect Tingyan HeYanyan HuangJun Yang Letter to Editor 18 May 2020 Pages: 571 - 575
European Society for Immunodeficiencies (ESID) and European Reference Network on Rare Primary Immunodeficiency, Autoinflammatory and Autoimmune Diseases (ERN RITA) Complement Guideline: Deficiencies, Diagnosis, and Management Nicholas BrodszkiAshley Frazer-AbelStephen Jolles Original Article Open access 17 February 2020 Pages: 576 - 591
Immunological and Clinical Phenotyping in Primary Antibody Deficiencies: a Growing Disease Spectrum Junghee J. ShinDaniel LiauwInsoo Kang Original Article 02 April 2020 Pages: 592 - 601
Health-Related Quality of Life and Multidimensional Fatigue Scale in Children with Primary Immunodeficiencies Saida Ridao-ManonellasAnna Fábregas-BofillPere Soler-Palacín Original Article 15 April 2020 Pages: 602 - 609
Urogenital Abnormalities in Adenosine Deaminase Deficiency Roberta PajnoLucia PacilloAlessandro Aiuti Original Article Open access 19 April 2020 Pages: 610 - 618
Failure to Prevent Severe Graft-Versus-Host Disease in Haploidentical Hematopoietic Cell Transplantation with Post-Transplant Cyclophosphamide in Chronic Granulomatous Disease Mark PartaDianne HilligossElizabeth M. Kang Original Article 20 April 2020 Pages: 619 - 624
BCG-Related Inflammatory Syndromes in Severe Combined Immunodeficiency After TCRαβ+/CD19+ Depleted HSCT Alexandra LaberkoDaria YukhachevaAnna Shcherbina Original Article 06 May 2020 Pages: 625 - 636
Homozygous IL1RN Mutation in Siblings with Deficiency of Interleukin-1 Receptor Antagonist (DIRA) Vahid ZiaeeLeila YoussefianJouni Uitto Letter to Editor 13 March 2020 Pages: 637 - 642
The IL1RN Mutation Creating the Most-Upstream Premature Stop Codon Is Hypomorphic Because of a Reinitiation of Translation Kunihiko MoriyaSaori KadowakiToshiyuki Fukao Letter to Editor 17 March 2020 Pages: 643 - 645
Correction to: the IL1RN Mutation Creating the Most-Upstream Premature Stop Codon Is Hypomorphic because of a Reinitiation of Translation Kunihiko MoriyaSaori KadowakiToshiyuki Fukao Correction 04 May 2020 Pages: 646 - 646
Compound Heterozygous Mutations of IL12RB1 in a Patient with Selective Defects in Th17 Differentiation Ming LiuBingtai LuYuxia Zhang Letter to Editor 27 March 2020 Pages: 647 - 652
Management of Chronic Immune Thrombocytopenia and Presumed Autoimmune Hepatitis in a Child with IKAROS Haploinsufficiency Daniel J. GrothMadhavi M. LakkarajaShipra M. Kaicker Letter to Editor 21 April 2020 Pages: 653 - 657
Novel Compound Heterozygote Variations in FADD Identified to Cause FAS-Associated Protein with Death Domain Deficiency Lisa A. KohnJoseph D. LongCaroline Y. Kuo Letter to Editor Open access 29 April 2020 Pages: 658 - 661
Novel Pathogenic C2 Variant Associated with Disseminated GBS Infection Emma C. PhillipsMonica GuptaMonica G. Lawrence Letter to Editor 08 May 2020 Pages: 662 - 664
A Case of STK4 Deficiency with Complications Evoking Mycobacterial Infection Nesrine RadwanRasha El-OwaidyShereen Medhat Reda Letter to Editor 11 May 2020 Pages: 665 - 669