Antonia P. Van Gorkom-Laros

Nijmegen, GE, Netherlands

Last Updated: 09/26/2026

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Found 21 publications

Tachyphylaxis and reproducibility of desmopressin response in perioperative persons with nonsevere hemophilia A: implications for clinical practice.

Tachyphylaxis and reproducibility of desmopressin response in perioperative persons with nonsevere hemophilia A: implications for clinical practice.

Journal: Research and practice in thrombosis and haemostasis
Published: August 22, 2023

Major differences in clinical presentation, diagnosis and management of men and women with autosomal inherited bleeding disorders.

Major differences in clinical presentation, diagnosis and management of men and women with autosomal inherited bleeding disorders.

Journal: EClinicalMedicine
Published: October 29, 2020

Specific proteome changes in platelets from individuals with GATA1-, GFI1B-, and RUNX1-linked bleeding disorders.

Specific proteome changes in platelets from individuals with GATA1-, GFI1B-, and RUNX1-linked bleeding disorders.

Journal: Blood
Published: July 17, 2020

Clinically relevant differences between assays for von Willebrand factor activity.

Clinically relevant differences between assays for von Willebrand factor activity.

Journal: Journal of thrombosis and haemostasis : JTH
Published: June 07, 2018

Population pharmacokinetics of factor IX in hemophilia B patients undergoing surgery.

Population pharmacokinetics of factor IX in hemophilia B patients undergoing surgery.

Journal: Journal of thrombosis and haemostasis : JTH
Published: March 30, 2018

Perioperative replacement therapy in haemophilia B: An appeal to "B" more precise.

Perioperative replacement therapy in haemophilia B: An appeal to "B" more precise.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia
Published: February 14, 2018

Analysis of current perioperative management with Haemate® P/Humate P® in von Willebrand disease: Identifying the need for personalized treatment.

Analysis of current perioperative management with Haemate® P/Humate P® in von Willebrand disease: Identifying the need for personalized treatment.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia
Published: January 31, 2018

Plasma levels of plasminogen activator inhibitor-1 and bleeding phenotype in patients with von Willebrand disease.

Plasma levels of plasminogen activator inhibitor-1 and bleeding phenotype in patients with von Willebrand disease.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia
Published: January 24, 2017

How do patients and professionals differentiate between intra-articular joint bleeds and acute flare-ups of arthropathy in patients with haemophilia?

How do patients and professionals differentiate between intra-articular joint bleeds and acute flare-ups of arthropathy in patients with haemophilia?

Journal: Haemophilia : the official journal of the World Federation of Hemophilia
Published: September 29, 2015

Joint surgery in von Willebrand disease: a multicentre cross-sectional study.

Joint surgery in von Willebrand disease: a multicentre cross-sectional study.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia
Published: August 31, 2015

Perioperative treatment of hemophilia A patients: blood group O patients are at risk of bleeding complications.

Perioperative treatment of hemophilia A patients: blood group O patients are at risk of bleeding complications.

Journal: Journal of thrombosis and haemostasis : JTH
Published: July 10, 2015

Clinical phenotype in genetically confirmed von Willebrand disease type 2N patients reflects a haemophilia A phenotype.

Clinical phenotype in genetically confirmed von Willebrand disease type 2N patients reflects a haemophilia A phenotype.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia
Published: May 02, 2015
Showing 1-12 of 21

Last Updated: 09/26/2026