V Vicente-Garcia
Murcia, MU, Spain
Last Updated: 09/26/2026
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Found 225 publications
De novo mutations in antithrombin deficiency: high frequency and heterogeneous mechanisms.
Journal: Haematologica
Published: August 04, 2025
An innovative modelling proposal for the blood supply chain.
Journal: Vox sanguinis
Published: May 09, 2025
Thrombotic risk and features of patients with inferior vena cava agenesis: a multicentre, retrospective, observational study.
Journal: The Lancet. Haematology
Published: January 11, 2024
Factor XI in Carriers of Antiphospholipid Antibodies: Elevated Levels Associated with Symptomatic Thrombotic Cases, While Low Levels Linked to Asymptomatic Cases.
Journal: International journal of molecular sciences
Published: October 06, 2023
Suramin, a drug for the treatment of trypanosomiasis, reduces the prothrombotic and metastatic phenotypes of colorectal cancer cells by inhibiting hepsin.
Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
Published: August 30, 2023
The whole is greater than the sum of its parts: Long-read sequencing for solving clinical problems in haematology.
Journal: Journal of cellular and molecular medicine
Published: July 24, 2023
Congenital factor XI deficiency and risk of heart failure in humans.
Journal: Journal of thrombosis and haemostasis : JTH
Published: June 06, 2023
Venetoclax is a potent hepsin inhibitor that reduces the metastatic and prothrombotic phenotypes of hepsin-expressing colorectal cancer cells.
Journal: Frontiers in molecular biosciences
Published: March 09, 2023
Usefulness and Limitations of Multiple Ligation-Dependent Probe Amplification in Antithrombin Deficiency.
Journal: International journal of molecular sciences
Published: February 10, 2023
Impact of genetic structural variants in factor XI deficiency: identification, accurate characterization, and inferred mechanism by long-read sequencing.
Journal: Journal of thrombosis and haemostasis : JTH
Published: December 23, 2022
Platelet transcriptome analysis in patients with germline RUNX1 mutations.
Journal: Journal of thrombosis and haemostasis : JTH
Published: August 22, 2022
Long-Read Sequencing Identifies the First Retrotransposon Insertion and Resolves Structural Variants Causing Antithrombin Deficiency.
Journal: Thrombosis and haemostasis
Published: June 28, 2022
Last Updated: 09/26/2026