Primary Immunodeficiency Classification on Smartphone Leïla JeddaneHind OuairAhmed Aziz Bousfiha Announcement 25 November 2016 Pages: 1 - 2
Comments on J Clin Immunol (2014) 34:633–641 DOI 10.1007/s10875-014-0061-0 Dirk Roos Letter to Editor 31 August 2016 Pages: 3 - 4
Erratum to: Clinical and Molecular Features of 38 Children with Chronic Granulomatous Disease in Mainland China Huan XuWen TianLi-Ping Jiang Erratum 16 November 2016 Pages: 5 - 6
OL-EDA-ID Syndrome: a Novel Hypomorphic NEMO Mutation Associated with a Severe Clinical Presentation and Transient HLH Silvia RicciFrancesca RomanoChiara Azzari Letter to Editor Open access 12 November 2016 Pages: 7 - 11
AD Hyper-IgE Syndrome Due to a Novel Loss-of-Function Mutation in STAT3: a Diagnostic Pursuit Won by Clinical Acuity Leen MoensHeidi SchaballieIsabelle Meyts Letter to Editor 14 November 2016 Pages: 12 - 17
Low T Cell Numbers Resembling T−B+ SCID in a Patient with Wiskott–Aldrich Syndrome and the Outcome of Two Hematopoietic Stem Cell Transplantations Deniz CagdasSelin Aytacİlhan Tezcan Letter to Editor 30 November 2016 Pages: 18 - 21
Lack of Clinical Hypersensitivity to Penicillin Antibiotics in Common Variable Immunodeficiency Heather HartmanKarrie SchneiderJohn Routes Letter to Editor 22 November 2016 Pages: 22 - 24
A 13-Year-Old Child with Lupus-Like Nephritis and 22q11 Microduplication Syndrome Zoi Dorothea PanaMaria StamouMaria Hatzistilianou Letter to Editor 04 November 2016 Pages: 25 - 26
Skin Necrosis Following Subcutaneous Immunoglobulin (SCIg) Emily CarneMark PonsfordStephen Jolles Letter to Editor 28 October 2016 Pages: 27 - 28
Postpartum HLA-Matched Bone Marrow Donation from Mother to Neonate for Reticular Dysgenesis Gregory M. T. GuilcherNicola A. M. WrightVictor A. Lewis Letter to Editor 03 December 2016 Pages: 29 - 31
Large Deletion of MAGT1 Gene in a Patient with Classic Kaposi Sarcoma, CD4 Lymphopenia, and EBV Infection Immacolata BrigidaMaria ChiriacoAndrea Finocchi Letter to Editor Open access 21 October 2016 Pages: 32 - 35
Early Identification of Lung Fungal Infections in Chronic Granulomatous Disease (CGD) Using Multidetector Computer Tomography Maria Pia BondioniVassilios LougarisAlessandro Plebani Original Article 21 October 2016 Pages: 36 - 41
Identification of Heterozygous Single- and Multi-exon Deletions in IL7R by Whole Exome Sequencing Karin R. EngelhardtYaobo XuSophie Hambleton Original Article Open access 02 November 2016 Pages: 42 - 50
Newborn Screening for Severe Primary Immunodeficiency Diseases in Sweden—a 2-Year Pilot TREC and KREC Screening Study Michela BarbaroAnnika OhlssonLennart Hammarström Original Article Open access 21 November 2016 Pages: 51 - 60
Resolution of Multifocal Epstein-Barr Virus-Related Smooth Muscle Tumor in a Patient with GATA2 Deficiency Following Hematopoietic Stem Cell Transplantation Mark PartaJennifer Cuellar-RodriguezDennis D. Hickstein Original Article 06 December 2016 Pages: 61 - 66
Targeted Sequencing and Immunological Analysis Reveal the Involvement of Primary Immunodeficiency Genes in Pediatric IBD: a Japanese Multicenter Study Tasuku SuzukiYoji SasaharaShigeo Kure Original Article 17 October 2016 Pages: 67 - 79
Idiopathic Non-histaminergic Angioedema: Successful Treatment with Omalizumab in Five Patients Charles FaisantAurélie Du ThanhLaurence Bouillet Original Article 08 November 2016 Pages: 80 - 84
Hematopoietic Stem Cell Transplantation for XIAP Deficiency in Japan Shintaro OnoTsubasa OkanoHirokazu Kanegane Original Article 04 November 2016 Pages: 85 - 91
A CD57+ CTL Degranulation Assay Effectively Identifies Familial Hemophagocytic Lymphohistiocytosis Type 3 Patients Masayuki HoriTakahiro YasumiToshio Heike Original Article 28 November 2016 Pages: 92 - 99
