Agustin Alen-Rodriguez
Toledo, CM, Spain
Last Updated: 09/26/2026
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Found 14 publications
Optimizing Surgical Approaches for Patients with Inherited Factor VII Deficiency.
Journal: Thrombosis and haemostasis
Published: December 24, 2025
Molecular Pathogenesis of Inherited Platelet Dysfunction.
Journal: Biomolecules
Published: October 05, 2025
De novo mutations in antithrombin deficiency: high frequency and heterogeneous mechanisms.
Journal: Haematologica
Published: August 04, 2025
Insights into the clinical, platelet and genetic landscape of inherited thrombocytopenia with malignancy risk.
Journal: British journal of haematology
Published: March 08, 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
Targeted long-read sequencing identifies and characterizes structural variants in cases of inherited platelet disorders.
Journal: Journal of thrombosis and haemostasis : JTH
Published: June 23, 2023
Platelet transcriptome analysis in patients with germline RUNX1 mutations.
Journal: Journal of thrombosis and haemostasis : JTH
Published: August 22, 2022
Inherited Platelet Disorders: An Updated Overview.
Journal: International journal of molecular sciences
Published: March 31, 2021
Management of acquired hemophilia A: results from the Spanish registry.
Journal: Blood advances
Published: March 01, 2021
A novel genetic variant in PTGS1 affects N-glycosylation of cyclooxygenase-1 causing a dominant-negative effect on platelet function and bleeding diathesis.
Journal: American journal of hematology
Published: October 22, 2020
Identification of the first large intronic deletion responsible of type I antithrombin deficiency not detected by routine molecular diagnostic methods.
Journal: British journal of haematology
Published: April 04, 2019
Last Updated: 09/26/2026