Rosella Mari
Ferrara, Italy
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 9 publications
Coagulation Factor XII Levels and Intrinsic Thrombin Generation in Multiple Sclerosis.
Journal: Frontiers in neurology
Published: January 31, 2018
Differential functional readthrough over homozygous nonsense mutations contributes to the bleeding phenotype in coagulation factor VII deficiency.
Journal: Journal of thrombosis and haemostasis : JTH
Published: May 19, 2016
An Exon-Specific U1snRNA Induces a Robust Factor IX Activity in Mice Expressing Multiple Human FIX Splicing Mutants.
Journal: Molecular therapy. Nucleic acids
Published: February 10, 2016
Coagulation Factor XIIIA (F13A1): Novel Perspectives in Treatment and Pharmacogenetics.
Journal: Current pharmaceutical design
Published: October 30, 2015
The carboxyl-terminal region is NOT essential for secreted and functional levels of coagulation factor X.
Journal: Journal of thrombosis and haemostasis : JTH
Published: May 04, 2015
Factor XIII-A dynamics in acute myocardial infarction: a novel prognostic biomarker?
Journal: Thrombosis and haemostasis
Published: November 17, 2014
Replacement of the Y450 (c234) phenyl ring in the carboxyl-terminal region of coagulation factor IX causes pleiotropic effects on secretion and enzyme activity.
Journal: FEBS letters
Published: June 27, 2013
Natural and engineered carboxy-terminal variants: decreased secretion and gain-of-function result in asymptomatic coagulation factor VII deficiency.
Journal: Haematologica
Published: December 20, 2011
Showing 1-9 of 9
Last Updated: 09/26/2026