Liliana Mannucci
Rome, Italy
Last Updated: 09/26/2026
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Found 9 publications
Unexpected genomic architecture in a sporadic case of C1-INH Hereditary Angioedema: the hidden heritability.
Journal: Orphanet journal of rare diseases
Published: February 14, 2025
The Senolytic Effect of Indole-3-Carbinol (I3C) on Mouse Embryonic (MEF) and Human Fibroblast Cell Lines.
Journal: International journal of molecular sciences
Published: September 30, 2024
Carrier frequency of CFTR variants in the non-Caucasian populations by genome aggregation database (gnomAD)-based analysis.
Journal: Annals of human genetics
Published: February 20, 2020
Mutation analysis of the FBN1 gene in a cohort of patients with Marfan Syndrome: A 10-year single center experience.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: July 31, 2019
Lp-PLA2, a new biomarker of vascular disorders in metabolic diseases.
Journal: International journal of immunopathology and pharmacology
Published: February 02, 2019
Drug repositioning screening identifies etravirine as a potential therapeutic for friedreich's ataxia.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: July 10, 2018
Performance characteristics of lipoprotein-associated phospholipase A2 activity assay on the Dimension Vista analyser and preliminary study of a healthy Italian population.
Journal: Biochemia medica
Published: May 02, 2017
Beta-sitosterolaemia: a new nonsense mutation in the ABCG5 gene.
Journal: European journal of clinical investigation
Published: November 03, 2007
Showing 1-9 of 9
Last Updated: 09/26/2026