Samantha Pasca

Trento, Italy

Last Updated: 09/26/2026

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Found 57 publications

The effective use of platelet-rich plasma (PRP) in treating a severe traumatic knee injury in a child with hemophilia A.

The effective use of platelet-rich plasma (PRP) in treating a severe traumatic knee injury in a child with hemophilia A.

Journal: Blood transfusion = Trasfusione del sangue

Published: December 20, 2025

Factor II and Factor V Deficiencies: Current Management, Care Gaps and Call to Action for Therapeutic Advances.

Factor II and Factor V Deficiencies: Current Management, Care Gaps and Call to Action for Therapeutic Advances.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia

Published: September 24, 2025

Gender difference among blood donors: should laboratory ranges be changed?

Gender difference among blood donors: should laboratory ranges be changed?

Journal: Blood transfusion = Trasfusione del sangue

Published: March 10, 2025

Bleeding Episodes in Patients With Haemophilia B Receiving Prophylactic Factor IX Treatment: A Systematic Review and Meta-Analysis.

Bleeding Episodes in Patients With Haemophilia B Receiving Prophylactic Factor IX Treatment: A Systematic Review and Meta-Analysis.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia

Published: October 07, 2024

Acquired Hemophilia A after SARS-CoV-2 Immunization: A Narrative Review of a Rare Side Effect.

Acquired Hemophilia A after SARS-CoV-2 Immunization: A Narrative Review of a Rare Side Effect.

Journal: Vaccines

Published: May 09, 2024

Personalized Prophylaxis with myPKFiTCE: A Real-World Cost-Effectiveness Analysis in Haemophilia A Patients.

Personalized Prophylaxis with myPKFiTCE: A Real-World Cost-Effectiveness Analysis in Haemophilia A Patients.

Journal: Medicina (Kaunas, Lithuania)

Published: October 16, 2023

Joint Dysfunction as a Cause of Spontaneous Subclinical Bleeding in Infants with Hemophilia.

Joint Dysfunction as a Cause of Spontaneous Subclinical Bleeding in Infants with Hemophilia.

Journal: Journal of clinical medicine

Published: September 05, 2023

Specific serum biomarkers to assess the bone health in a group of hemophilia A carriers: Data from the CAR.BONE study.

Specific serum biomarkers to assess the bone health in a group of hemophilia A carriers: Data from the CAR.BONE study.

Journal: Thrombosis research

Published: July 27, 2023

Bilirubin color interference on prothrombin time and activated partial thromboplastin time tests assessed in patients with liver disease.

Bilirubin color interference on prothrombin time and activated partial thromboplastin time tests assessed in patients with liver disease.

Journal: Clinical chemistry and laboratory medicine

Published: April 07, 2023

Correction to: The pharmacokinetics of recombinant FXIII (catridecacog) from the MENTORTM2 trial to a real-world study: a head-to-head comparison.

Correction to: The pharmacokinetics of recombinant FXIII (catridecacog) from the MENTORTM2 trial to a real-world study: a head-to-head comparison.

Journal: Journal of thrombosis and thrombolysis

Published: November 23, 2022

Emicizumab in acquired hemophilia A: pros and cons of a new approach to the prevention and treatment of bleeding.

Emicizumab in acquired hemophilia A: pros and cons of a new approach to the prevention and treatment of bleeding.

Journal: Blood transfusion = Trasfusione del sangue

Published: October 20, 2022

Very high risk of intracranial hemorrhage and severe outcomes in adult patients with mild hemophilia: Sub-analysis of the EMO.REC Registry.

Very high risk of intracranial hemorrhage and severe outcomes in adult patients with mild hemophilia: Sub-analysis of the EMO.REC Registry.

Journal: Thrombosis research

Published: September 19, 2022

Showing 1-12 of 57

Last Updated: 09/26/2026