Federica Barzaghi
Milan, Italy
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 82 publications
Pregnancy and lactation during anifrolumab treatment in systemic lupus erythematosus.
Journal: Dermatology reports
Published: April 22, 2026
Gene therapy supports long-term reconstitution of patient hematopoietic stem cells in deficiency of adenosine deaminase 2.
Journal: Molecular therapy. Methods & clinical development
Published: September 16, 2025
Uncommon causal variants of the ADA2 gene in patients with reduced enzyme activity and nonconfirmatory genetic testing.
Journal: The journal of allergy and clinical immunology. In practice
Published: July 27, 2025
Long-Term Effects of Atidarsagene Autotemcel for Metachromatic Leukodystrophy.
Journal: The New England journal of medicine
Published: April 23, 2025
Somatic deficiency of the human E3 ubiquitin ligase CBL in leukocytes impairs B cell but not T cell development and function.
Journal: Nature immunology
Published: December 16, 2024
One hundred thirty-four germ line PU.1 variants and the agammaglobulinemic patients carrying them.
Journal: Blood
Published: September 09, 2024
Report of the Italian Cohort with Activated Phosphoinositide 3-Kinase δ Syndrome in the Target Therapy Era.
Journal: Journal of clinical immunology
Published: August 12, 2024
Consensus of the Italian Primary Immunodeficiency Network on the use and interpretation of genetic testing for diagnosing inborn errors of immunity.
Journal: The Journal of allergy and clinical immunology
Published: July 22, 2024
Early bone marrow alterations in patients with adenosine deaminase 2 deficiency across disease phenotypes and severities.
Journal: The Journal of allergy and clinical immunology
Published: May 06, 2024
Early skeletal outcomes after hematopoietic stem and progenitor cell gene therapy for Hurler syndrome.
Journal: Science translational medicine
Published: May 01, 2024
Autoinflammation in patients with leukocytic CBL loss of heterozygosity is caused by constitutive ERK-mediated monocyte activation.
Journal: The Journal of clinical investigation
Published: April 02, 2024
Last Updated: 09/26/2026