Successful Bone Marrow Transplantation for XMEN: Hemorrhagic Risk Uncovered Dimana DimitrovaJeremy J. RoseJennifer A. Kanakry Letter to Editor 23 November 2018 Pages: 1 - 3
MonoMAC Syndrome Caused by a Novel GATA2 Mutation Successfully Treated by Allogeneic Hematopoietic Stem Cell Transplantation Maria Francisca Moraes-FontesÍris CaramalhoManuel Abecasis Letter to Editor 26 November 2018 Pages: 4 - 6
Monoclonal Gammopathy of Unclear Significance in a Child with Wiskott-Aldrich Syndrome: a Rare Occurrence Rashmi RikhiSagar BhattadSurjit Singh Letter to Editor 03 January 2019 Pages: 7 - 10
A Novel STK4 Mutation Presenting with Juvenile Idiopathic Arthritis and Epidermodysplasia Verruciformis Samin SharafianVahid ZiaeeNima Parvaneh Letter to Editor 05 January 2019 Pages: 11 - 14
Two Prenatal Cases of Hyper-IgE Syndrome Makiko EgawaKohsuke ImaiNaoyuki Miyasaka Letter to Editor 07 January 2019 Pages: 15 - 18
Successful Treatment with SCIG of a Child with Refractory Chronic ITP Anna KarastanevaDaniela S. KlobassaMarkus G. Seidel Letter to Editor 10 January 2019 Pages: 19 - 22
Damaging BTK Variant Demonstrated by Carrier, Allele-Specific BTK Expression in B Cells and Monocytes Mary T. Bausch-JurkenMary HintermeyerJohn Routes Letter to Editor 10 January 2019 Pages: 23 - 25
Childhood Hodgkin Lymphoma: Think DADA2 Fahad AlabbasGhaleb ElyamanyIsabelle Meyts Letter to Editor 14 January 2019 Pages: 26 - 29
Autoimmunity and Inflammation in CVID: a Possible Crosstalk between Immune Activation, Gut Microbiota, and Epigenetic Modifications Silje F. JørgensenBørre FevangPål Aukrust Original Article 21 November 2018 Pages: 30 - 36
Hematopoietic Stem Cell Transplantation in Patients with Heterozygous STAT1 Gain-of-Function Mutation Ayca KiykimLouis Marie CharbonnierSafa Baris Original Article 13 December 2018 Pages: 37 - 44
Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group Katharina SchützDiana Alecsandrufor the Chest CT in Antibody Deficiency Group Original Article 13 December 2018 Pages: 45 - 54
Progressive Multifocal Leukoencephalopathy in Primary Immunodeficiencies Jérôme HadjadjAurélien GuffroyFelipe Suarez Original Article 14 December 2018 Pages: 55 - 64
Lymphocyte Apoptosis and FAS Expression in Patients with 22q11.2 Deletion Syndrome Dina M. AresvikTorstein ØverlandTore G. Abrahamsen Original Article 19 December 2018 Pages: 65 - 74
DDX58 and Classic Singleton-Merten Syndrome Carlos R. FerreiraYanick J. CrowTracy A. Briggs Original Article Open access 20 December 2018 Pages: 75 - 80
Rubella Virus-Associated Cutaneous Granulomatous Disease: a Unique Complication in Immune-Deficient Patients, Not Limited to DNA Repair Disorders David BuchbinderFabian HauckHans D. Ochs Original Article 03 January 2019 Pages: 81 - 89
Differing Performance of the Warning Signs for Immunodeficiency in the Diagnosis of Pediatric Versus Adult Patients in a Two-Center Tertiary Referral Population Jaclyn A. BjelacJennifer R. YonkofJames Fernandez Original Article 04 January 2019 Pages: 90 - 98
A Novel Missense LIG4 Mutation in a Patient With a Phenotype Mimicking Behçet’s Disease Ekim Z. TaskiranHafize E. SonmezSeza Ozen Original Article 08 January 2019 Pages: 99 - 105
Mosaicism of an ELANE Mutation in an Asymptomatic Mother Tomonari ShigemuraNorimoto KobayashiYozo Nakazawa Original Article 12 January 2019 Pages: 106 - 111
Outcomes for Nitazoxanide Treatment in a Case Series of Patients with Primary Immunodeficiencies and Rubella Virus-Associated Granuloma Ludmila PerelyginaDavid BuchbinderKathleen E. Sullivan Original Article 24 January 2019 Pages: 112 - 117
TREX-1-Related Disease Associated with the Presence of Cryofibrinogenemia C. ParadisM. Cadieux-DionP. Begin Original Article 26 January 2019 Pages: 118 - 125