Michela Lorrai
Cagliari, 09124, Italy
Last Updated: 09/26/2026
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Found 10 publications
Whole-Exome Sequencing Identifies Novel Genetic Variants Associated with Unexplained Neurodevelopmental Disorders in Children.
Journal: International journal of molecular sciences
Published: December 27, 2025
MICA-129Met/Val as a therapeutic compass in idiopathic pulmonary fibrosis: prognosis and antifibrotic benefit.
Journal: Frontiers in immunology
Published: October 10, 2025
Telomere dysfunction and mucociliary impairment drive idiopathic pulmonary fibrosis susceptibility: insights from a Sardinian whole-exome study.
Journal: BMJ open respiratory research
Published: July 11, 2025
The role of HLA-G in primary biliary cholangitis and response to therapy.
Journal: Frontiers in immunology
Published: February 28, 2025
Impact of the Human Leukocyte Antigen Complex on Idiopathic Pulmonary Fibrosis Development and Progression in the Sardinian Population.
Journal: International journal of molecular sciences
Published: January 23, 2025
PPP2R5D-Related Neurodevelopmental Disorder and Multiple Haemangiomas: A Novel Phenotypic Trait?
Journal: Pediatric reports
Published: October 16, 2024
MICA and NKG2D gene polymorphisms influence graft survival, and response to therapy in kidney transplantation.
Journal: Frontiers in immunology
Published: May 30, 2024
Systemic lupus erythematosus occurring in a patient with Niemann-Pick type B disease.
Journal: Lupus
Published: February 27, 2015
Switch to icatibant in a patient affected by hereditary angioedema with high disease activity: a case report.
Journal: International journal of immunopathology and pharmacology
Published: April 18, 2012
Showing 1-10 of 10
Last Updated: 09/26/2026