Haemophilia management is not uniform among countries, even within western Europe, that have close economic, social and cultural relationship. The European Paediatric Network PedNet aims to share experiences in the field of the care of boys with haemophilia. In 1998, a PedNet survey has shown significant disparities in 20 centres from 16 countries, particularly as regards the implementation of prophylaxis regimen. This survey has been updated in 2003 to describe the current status of haemophilia management in 22 centres and the changing pattern of care of boys with severe haemophilia in western Europe. Regular, continuous long-term prophylaxis is provided in all PedNet centres, more than 50% and 80-100% of boys being treated this way in 20/...
INTRODUCTION: The prophylactic regimen in children with severe haemophilia is suggested in various p...
The aim of this study was to determine the clinical conditions of patients with haemophilia within E...
Replacement of the congenitally deficient factor VIII or IX through plasma-derived or recombinant co...
A survey was made of the current status of treatment of haemophilic boys at 20 centres in 16 Europea...
Although the regular replacement of clotting factor concentrates (prophylaxis) has been well establi...
The practice of prophylactic treatment of boys with severe haemophilia has been evaluated in our cen...
Introduction: Haemophilia treatment varies significantly between individuals, countries and regions ...
The development of recombinant FVIII (rFVIII) products, fuelled by the need for improved safety of t...
INTRODUCTION: Haemophilia treatment varies significantly between individuals, countries and regions ...
Introduction: Haemophilia treatment varies significantly between individuals, countries and regions ...
This paper reports the findings of a global survey of practice patterns for the management of patien...
A multicentre, international, cross-sectional study was carried out in the frame of field testing of...
In 2009, a questionnaire was circulated to 19 national haemophilia patient organizations in Europe a...
INTRODUCTION: The prophylactic regimen in children with severe haemophilia is suggested in various p...
The aim of this study was to determine the clinical conditions of patients with haemophilia within E...
INTRODUCTION: The prophylactic regimen in children with severe haemophilia is suggested in various p...
The aim of this study was to determine the clinical conditions of patients with haemophilia within E...
Replacement of the congenitally deficient factor VIII or IX through plasma-derived or recombinant co...
A survey was made of the current status of treatment of haemophilic boys at 20 centres in 16 Europea...
Although the regular replacement of clotting factor concentrates (prophylaxis) has been well establi...
The practice of prophylactic treatment of boys with severe haemophilia has been evaluated in our cen...
Introduction: Haemophilia treatment varies significantly between individuals, countries and regions ...
The development of recombinant FVIII (rFVIII) products, fuelled by the need for improved safety of t...
INTRODUCTION: Haemophilia treatment varies significantly between individuals, countries and regions ...
Introduction: Haemophilia treatment varies significantly between individuals, countries and regions ...
This paper reports the findings of a global survey of practice patterns for the management of patien...
A multicentre, international, cross-sectional study was carried out in the frame of field testing of...
In 2009, a questionnaire was circulated to 19 national haemophilia patient organizations in Europe a...
INTRODUCTION: The prophylactic regimen in children with severe haemophilia is suggested in various p...
The aim of this study was to determine the clinical conditions of patients with haemophilia within E...
INTRODUCTION: The prophylactic regimen in children with severe haemophilia is suggested in various p...
The aim of this study was to determine the clinical conditions of patients with haemophilia within E...
Replacement of the congenitally deficient factor VIII or IX through plasma-derived or recombinant co...