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Human Genetics|December 6, 2005
Analysis of families with common variable immunodeficiency (CVID) and IgA deficiency suggests linkage of CVID to chromosome 16qAlejandro A Schäffer, Jessica Pfannstiel, A David B Webster, et al.Journal of Clinical Gastroenterology|April 24, 2007
Diversion of the fecal stream resolves ulcerative colitis complicating chronic granulomatous disease in an adult patientVincenzo Villanacci, Diego Falchetti, Barbara Liserre, et al.European Journal of Haematology|December 23, 2004
Re-immunisation schedule in leukaemic children after intensive chemotherapy: a possible strategyFrancesca Fioredda, Alessandro Plebani, Guia Hanau, et al.Journal of Computer Assisted Tomography|September 21, 2007
Pulmonary and sinusal changes in 45 patients with primary immunodeficiencies: computed tomography evaluationMaria Pia Bondioni, Marzia Duse, Alessandro Plebani, et al.Journal of Clinical Immunology|February 1, 2014
Autosomal recessive agammaglobulinemia: a novel non-sense mutation in CD79aAbbas Khalili, Alessandro Plebani, Massimiliano Vitali, et al.Journal of Clinical Immunology|April 12, 2014
Autosomal recessive agammaglobulinemia: the third case of Igβ deficiency due to a novel non-sense mutationVassilios Lougaris, Massimiliano Vitali, Manuela Baronio, et al.Clinical Immunology (Orlando, Fla.)|December 1, 2018
Early B cell developmental impairment with progressive B cell deficiency in NFKB2 mutated CVID disease without autoimmunityVassilios Lougaris, Daniele Moratto, Manuela Baronio, et al.European Journal of Pediatrics|November 26, 2002
Mutations of the X-linked lymphoproliferative disease gene SH2D1A mimicking common variable immunodeficiencyAnnarosa Soresina, Vassilis Lougaris, Silvia Giliani, et al.The Journal of Pediatrics|February 14, 2003
Disseminated cryptosporidium infection in an infant with hyper-IgM syndrome caused by CD40 deficiencyNecil Kutukculer, Daniele Moratto, Yesim Aydinok, et al.Italian Journal of Pediatrics|November 14, 2014
Severe congenital neutropenia due to G6PC3 deficiency: early and delayed phenotype in two patients with two novel mutationsLucia Dora Notarangelo, Gianfranco Savoldi, Sara Cavagnini, et al.Pageof 25