Editorial, Journal of Clinical Immunology Jean-Laurent CasanovaVincent Bonagura Editorial 15 October 2019 Pages: 751 - 752
Survey of Infection Control Precautions for Patients with Severe Combined Immune Deficiency Brieanne A. DergousoffJoseph V. VayalumkalNicola A. M. Wright Original Article 20 August 2019 Pages: 753 - 761
Clinical and Molecular Features of Chronic Granulomatous Disease in Mainland China and a XL-CGD Female Infant Patient After Prenatal Diagnosis Shiyu WangTao WangLiping Jiang Original Article 27 August 2019 Pages: 762 - 775
Novel Gain-of-Function Mutation in Stat1 Sumoylation Site Leads to CMC/CID Phenotype Responsive to Ruxolitinib Tariq Al ShehriKimberly GilmourTimothy R. Leahy Original Article 11 September 2019 Pages: 776 - 785
Quality of Life of Patients with Wiskott Aldrich Syndrome and X-Linked Thrombocytopenia: a Study of the Primary Immune Deficiency Consortium (PIDTC), Immune Deficiency Foundation, and the Wiskott-Aldrich Foundation Ami J. ShahRobert SokolicMorton J. Cowan Original Article 16 October 2019 Pages: 786 - 794
A De Novo Frameshift Mutation in TNFAIP3 Impairs A20 Deubiquitination Function to Cause Neuropsychiatric Systemic Lupus Erythematosus Ruonan DuanQi LiuQiji Liu Original Article 17 October 2019 Pages: 795 - 804
Provider Perceptions of Quality of Life, Neurocognition, Physical Well-being, and Psychosocial Health in Patients with Primary Immunodeficiency/Immune Dysregulation Conditions Thomas F. MichniackiKelly J. WalkovichRoshini S. Abraham Original Article 26 October 2019 Pages: 805 - 813
Quality of Life Differences for Primary Immunodeficiency Patients on Home SCIG versus IVIG Christine AnterasianRichard DuongBob Geng Original Article Open access 01 November 2019 Pages: 814 - 822
STK4 Deficiency in a Patient with Immune Complex Glomerulonephritis, Salt-Losing Tubulopathy, and Castleman’s-Like Disease Bandar Al-SaudHuda AlajlanAnas M. Alazami Letter to Editor 23 August 2019 Pages: 823 - 826
Autosomal Dominant Hyper-IgE Syndrome Without Significantly Elevated IgE Carsten S. LarsenMette ChristiansenTrine H. Mogensen Letter to Editor 29 August 2019 Pages: 827 - 831
Successful Treatment of PAPA Syndrome with Dual Adalimumab and Tacrolimus Therapy Amika K. SoodDiana B. McShaneEveline Y. Wu Letter to Editor 30 August 2019 Pages: 832 - 835
Unusual Severe Seborrheic Dermatitis in Two Siblings with Autosomal Recessive Chronic Granulomatous Disease Nuria B. ZurroEdgar B. de Oliveira JuniorAntonio Condino-Neto Letter to Editor 03 September 2019 Pages: 836 - 838
Abnormal Newborn Screen in a WHIM Syndrome Infant Martin O. Evans IIDavid H. McDermottMaureen M. Petersen Letter to Editor 06 September 2019 Pages: 839 - 841
Homozygous Splice ADA2 Gene Mutation Causing ADA-2 Deficiency Herberto Jose Chong-NetoGesmar Rodrigues Silva SegundoNelson Augusto Rosário Letter to Editor 15 October 2019 Pages: 842 - 845
Management of ADA-Deficient SCID Patient on Adagen During Pregnancy Marissa ShamsLisa Kobrynski Letter to Editor 16 October 2019 Pages: 846 - 848
Interstitial Lung Disease Frequently Precedes CVID Diagnosis Leif G. HanitschKirsten WittkeCarmen Scheibenbogen Letter to Editor 22 October 2019 Pages: 849 - 851
Altered Monocyte Subsets in Patients with Chronic Idiopathic Neutropenia Nikoleta BizymiMaria VelegrakiHelen A. Papadaki Letter to Editor Open access 27 October 2019 Pages: 852 - 854
Serum Tryptase Cannot Differentiate Vancomycin-Induced Anaphylaxis From Red Man Syndrome Satoko NoguchiDaiki TakekawaKazuyoshi Hirota Letter to Editor 28 October 2019 Pages: 855 - 856
The Value of Chromosome Analysis to Interrogate Variants in DNMT3B Causing Immunodeficiency, Centromeric Instability, and Facial Anomaly Syndrome Type I (ICF1) Erinn S. KellnerPamela A. RathbunRebecca A. Marsh Letter to Editor 04 November 2019 Pages: 857 - 859
Correction to: Unusual Severe Seborrheic Dermatitis in Two Siblings with Autosomal Recessive Chronic Granulomatous Disease Nuria Bengala ZurroEdgar Borges de Oliveira JuniorAntonio Condino-Neto Correction 02 November 2019 Pages: 860 - 860