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Frontiers in Immunology|October 23, 2023
Decline of gastric cancer mortality in common variable immunodeficiency in the years 2018-2022Cinzia Milito, Federica Pulvirenti, Giulia Garzi, et al.
Epilepsia|March 4, 2014
Autosomal dominant partial epilepsy with auditory features: a new locus on chromosome 19q13.11-q13.31Francesca Bisulli, Ilaria Naldi, Sara Baldassari, et al.
Haematologica|August 2, 2007
Congenital amegakaryocytic thrombocytopenia: clinical and biological consequences of five novel mutationsAnna Savoia, Carlo Dufour, Franco Locatelli, 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.
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.
Blood|August 2, 2003
Functional defects of dendritic cells in patients with CD40 deficiencyStefania Fontana, Daniele Moratto, Surinder Mangal, et al.
Oncotarget|February 11, 2017
BRCA1 p.His1673del is a pathogenic mutation associated with a predominant ovarian cancer phenotypeRoberta Zuntini, Laura Cortesi, Daniele Calistri, et al.
International Journal of Molecular Sciences|March 14, 2026
Clonal Dynamics of FLT3-ITD from Diagnosis to Relapse: Ultra-Sensitive Patient-Specific Monitoring by ddPCRAlessandro Ferrando, Johanna Umurungi, Alice Costanza Danzero, et al.
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