Helen E. Platokouki

Athens, ESYE31, Greece

Last Updated: 09/26/2026

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Found 26 publications

Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database.

Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database.

Journal: Blood advances

Published: November 15, 2023

An open-label, multi-centre, post-marketing study to assess the efficacy and safety of a plasma-derived VWF/FVIII concentrate in patients with von Willebrand disease.

An open-label, multi-centre, post-marketing study to assess the efficacy and safety of a plasma-derived VWF/FVIII concentrate in patients with von Willebrand disease.

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

Published: December 05, 2022

Efficacy and safety of von Willebrand factor concentrate almost devoid of factor VIII (Wilfactin®) in paediatric patients under 6 years of age with severe von Willebrand disease.

Efficacy and safety of von Willebrand factor concentrate almost devoid of factor VIII (Wilfactin®) in paediatric patients under 6 years of age with severe von Willebrand disease.

Journal: Blood transfusion = Trasfusione del sangue

Published: December 10, 2021

ITI Treatment is not First-Choice Treatment in Children with Hemophilia A and Low-Responding Inhibitors: Evidence from a PedNet Study.

ITI Treatment is not First-Choice Treatment in Children with Hemophilia A and Low-Responding Inhibitors: Evidence from a PedNet Study.

Journal: Thrombosis and haemostasis

Published: June 24, 2020

The factor VIII treatment history of non-severe hemophilia A.

The factor VIII treatment history of non-severe hemophilia A.

Journal: Journal of thrombosis and haemostasis : JTH

Published: March 31, 2020

Inhibitor incidence in an unselected cohort of previously untreated patients with severe haemophilia B: a PedNet study.

Inhibitor incidence in an unselected cohort of previously untreated patients with severe haemophilia B: a PedNet study.

Journal: Haematologica

Published: October 11, 2019

Impact of target joint and FVIII inhibitor οn bone properties in children with haemophilia A: A peripheral quantitative computed tomography study.

Impact of target joint and FVIII inhibitor οn bone properties in children with haemophilia A: A peripheral quantitative computed tomography study.

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

Published: April 02, 2018

Risk Factors for the Progression from Low to High Titres in 260 Children with Severe Haemophilia A and Newly Developed Inhibitors.

Risk Factors for the Progression from Low to High Titres in 260 Children with Severe Haemophilia A and Newly Developed Inhibitors.

Journal: Thrombosis and haemostasis

Published: December 07, 2017

Vaccinations are not associated with inhibitor development in boys with severe haemophilia A.

Vaccinations are not associated with inhibitor development in boys with severe haemophilia A.

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

Published: November 19, 2017

Desmopressin in moderate hemophilia A patients: a treatment worth considering.

Desmopressin in moderate hemophilia A patients: a treatment worth considering.

Journal: Haematologica

Published: September 01, 2017

Tracheal stenosis in a paediatric patient with severe haemophilia A and FVIII inhibitors.

Tracheal stenosis in a paediatric patient with severe haemophilia A and FVIII inhibitors.

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

Published: August 22, 2017

Intracranial haemorrhage in children and adolescents with severe haemophilia A or B - the impact of prophylactic treatment.

Intracranial haemorrhage in children and adolescents with severe haemophilia A or B - the impact of prophylactic treatment.

Journal: British journal of haematology

Published: April 04, 2017

Showing 1-12 of 26

Last Updated: 09/26/2026