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Journal of the American Heart Association|June 29, 2014
Different degrees of NADPH oxidase 2 regulation and in vivo platelet activation: lesson from chronic granulomatous diseaseRoberto Carnevale, Lorenzo Loffredo, Valerio Sanguigni, et al.
The Journal of Allergy and Clinical Immunology|January 11, 2017
Impaired natural killer cell functions in patients with signal transducer and activator of transcription 1 (STAT1) gain-of-function mutationsGiovanna Tabellini, Donatella Vairo, Omar Scomodon, et al.
Haematologica|August 2, 2007
Congenital amegakaryocytic thrombocytopenia: clinical and biological consequences of five novel mutationsAnna Savoia, Carlo Dufour, Franco Locatelli, et al.
Molecular Cytogenetics|August 4, 2015
Cytogenetic and molecular characterization of a recombinant X chromosome in a family with a severe neurologic phenotype and macular degenerationPamela Magini, Monica Poscente, Simona Ferrari, et al.
International Journal of Molecular Sciences|September 27, 2025
Neuroinflammation in CTLA-4 Haploinsufficiency: Case Report of a New Variant with Remarkable Response to Targeted TherapyLetizia Baldini, Lucia Del Vecchio, Sara Cerasi, et al.
Clinical Immunology (Orlando, Fla.)|April 20, 2004
Search for poliovirus long-term excretors among patients affected by agammaglobulinemiaLucia Fiore, Alessandro Plebani, Gabriele Buttinelli, et al.
Cells|June 24, 2022
T-Cell Defects Associated to Lack of Spike-Specific Antibodies after BNT162b2 Full Immunization Followed by a Booster Dose in Patients with Common Variable Immune DeficienciesFederica Pulvirenti, Stefano Di Cecca, Matilde Sinibaldi, et al.
International Archives of Allergy and Immunology|September 1, 2006
Clinical, immunological and molecular characteristics of 37 Iranian patients with X-linked agammaglobulinemiaAsghar Aghamohammadi, Maurilia Fiorini, Mostafa Moin, et al.
Circulation|October 7, 2009
Hereditary deficiency of gp91(phox) is associated with enhanced arterial dilatation: results of a multicenter studyFrancesco Violi, Valerio Sanguigni, Roberto Carnevale, et al.
International Journal of Molecular Sciences|June 2, 2021
Detecting Variants in the NBN Gene While Testing for Hereditary Breast Cancer: What to Do Next?Roberta Zuntini, Elena Bonora, Laura Maria Pradella, et al.
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