Human Disease Phenotypes Associated With Mutations in TREX1 Gillian I. RiceMathieu P. RoderoYanick J. Crow CME REVIEW 04 March 2015 Pages: 235 - 243
A Female Patient with Incomplete Hemophagocytic Lymphohistiocytosis Caused by a Heterozygous XIAP Mutation Associated with Non-Random X-Chromosome Inactivation Skewed Towards the Wild-Type XIAP Allele Xi YangAkihiro HoshinoHirokazu Kanegane Astute Clinician Report 07 March 2015 Pages: 244 - 248
Overlap of Familial Mediterranean Fever and Hyper-IgD Syndrome in an Arabic Kindred Taha MoussaButhaina AladbeBasil M Fathalla Astute Clinician Report 24 February 2015 Pages: 249 - 253
A mutation in the human tetraspanin CD81 gene is expressed as a truncated protein but does not enable CD19 maturation and cell surface expression Felipe Vences-CatalánChiung-Chi KuoShoshana Levy Original Research 06 March 2015 Pages: 254 - 263
Long-Term Follow-up of STAT5B Deficiency in Three Argentinian Patients: Clinical and Immunological Features Liliana BezrodnikDaniela Di GiovanniMaría Isabel Gaillard Original Research 11 March 2015 Pages: 264 - 272
The Duesseldorf Warning Signs for Primary Immunodeficiency: Is it Time to Change the Rules? Petra LankischJulia SchiffnerHans-Jürgen Laws Original Research 08 March 2015 Pages: 273 - 279
RAG1 Deficiency May Present Clinically as Selective IgA Deficiency Tamaki KatoElena CrestaniShigeaki Nonoyama Original Research 06 March 2015 Pages: 280 - 288
Reduced Frequencies of Polyfunctional CMV-Specific T Cell Responses in Infants with Congenital CMV Infection Laura GibsonConstance M. BarysauskasKatherine Luzuriaga Original Research 25 February 2015 Pages: 289 - 301
Familial Hepatopulmonary Syndrome in Common Variable Immunodeficiency S. N. HolmesA. CondliffeD. S. Kumararatne Brief Communication 24 February 2015 Pages: 302 - 304
2015 CIS Annual Meeting: Immune Deficiency & Dysregulation North American Conference Abstracts 04 February 2015 Pages: 305 - 328