Response to the Letter to the Editor Regarding “Assessment of Local Adverse Reactions to Subcutaneous Immunoglobulin (SCIG) in Clinical Trials” Daniel SuezMark SteinLeman Yel Letter to Editor Open access 05 September 2017 Pages: 739 - 740
Fecal Calprotectin Rise in Chronic Granulomatous Disease-Associated Colitis Yumiko NakazawaToshinao KawaiMasafumi Onodera Letter to Editor 06 September 2017 Pages: 741 - 743
Response to the Letter to the Editor Regarding “Kinetics of Radiological Response of Thoracic Invasive Fungal Disease in Chronic Granulomatous Disease” Maria P. BondioniVassilios LougarisAlessandro Plebani Letter to Editor 08 October 2017 Pages: 744 - 745
Hematopoietic Stem Cell Transplantation in ADA2 Deficiency: Early Restoration of ADA2 Enzyme Activity and Disease Relapse upon Drop of Donor Chimerism Giorgia BucciolSelket DelafontaineIsabelle Meyts Letter to Editor 10 October 2017 Pages: 746 - 750
FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches Vera GalloEmilia CirilloClaudio Pignata CME Review 21 September 2017 Pages: 751 - 758
Preferential Reduction of Circulating Innate Lymphoid Cells Type 2 in Patients with Common Variable Immunodeficiency with Secondary Complications Is Part of a Broader Immune Dysregulation David FriedmannBaerbel KellerKlaus Warnatz Original Article 21 September 2017 Pages: 759 - 769
Effective Immunological Guidance of Genetic Analyses Including Exome Sequencing in Patients Evaluated for Hemophagocytic Lymphohistiocytosis Sandra AmmannKai Lehmbergthe HLH study of the GPOH Original Article 21 September 2017 Pages: 770 - 780
Early Versus Late Diagnosis of Complement Factor I Deficiency: Clinical Consequences Illustrated in Two Families with Novel Homozygous CFI Mutations Clara Franco-JaravaElena Álvarez de la CampaRoger Colobran Original Article 23 September 2017 Pages: 781 - 789
Multiple Presentations of LRBA Deficiency: a Single-Center Experience Sevgi Kostel BalSule HaskologluAydan Ikinciogullari Original Article 27 September 2017 Pages: 790 - 800
Functional Evaluation of an IKBKG Variant Suspected to Cause Immunodeficiency Without Ectodermal Dysplasia Glynis FransJutte van der Werff Ten BoschXavier Bossuyt Original Article 10 October 2017 Pages: 801 - 810
DOCK8 Deficiency Presenting as an IPEX-Like Disorder Fayhan J. AlroqiLouis-Marie CharbonnierTalal A. Chatila Original Article 23 October 2017 Pages: 811 - 819