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WFH 2014 World Congress

 

11-15 May 2014 Melbourne
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Discussion forum - WFH 2014 World Congress
    Topic - Database and Registries

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 Thread / Poster  Author  Replies  Last reply
be-Coag, The Internet Heamophilia Medical Record by NMOs  Patrick Finders-Binje 1      5/7/2014 10:15:00 PM  
A WEB SITE TO IMPROVE MANAGEMENT OF PATIENTS WITH INHERITED BLEEDING DISORDERS IN THE EMERGENCY DEPARTMENT: RESULTS AT 2 YEARS  Annarita Tagliaferri 1      5/5/2014 5:09:00 PM  
The Impact of Factor VIII Concentrate on the Development of Inhibitors in Children with Severe Hemophilia A: Turkish PUP Registry Study  Aysegul Unuvar 1      4/23/2014 7:03:00 PM  
Community Counts: A National Surveillance System For Bleeding And Clotting Disorders.  Marilyn Manco-Johnson 1      4/23/2014 7:02:00 PM  
RegHemo: first steps to an Integrated Information System in Hemophilia and other congenital coagulopathies  Ariel Triana-Usich 1      4/23/2014 5:50:00 PM  
Rationale and study design of TARGET H: An observational sTudy to Assess the feasibility of combining data from patient ReGistries in countries with developing healthcare systems to EvaluaTe Haemophilia management  Joachim Potgieter 1      4/23/2014 4:47:00 PM  
Australian Bleeding Disorders Registry the evolution over 25 years of a national database for people with bleeding disorders  John Rowell 1      4/23/2014 9:00:00 AM  
Data and demographics from the Australian Bleeding Disorders Registry (ABDR)  John Rowell 1      4/23/2014 8:54:00 AM  
Use of data and reporting to improve haemophilia care  bj ramsay 1      4/23/2014 7:57:00 AM  
MyABDR: an online personally controlled clinical tool for recording treatments and bleeds  Suzanne OCallaghan 1      4/23/2014 6:05:00 AM  
SINGLE CENTER REGISTRY OF RARE BLEEDING DISORDERS FROM TURKEY  Turkan PATIROGLU 1      4/23/2014 5:45:00 AM  
WFH Annual Global Survey: New Integrated Electronic Data Collection and Management System  Mark Brooker 1      4/22/2014 3:15:00 PM  
Update of National Hemophilia Registry of China  Feng Xue 1      4/18/2014 5:55:00 PM  
French online database on bleeding disorders NHEMO: pharmaceutical contributions to the multidisciplinary network.  Martine Pennetier 1      4/17/2014 6:32:00 PM  
French online database on bleeding disorders NHEMO: pharmaceutical contributions to the multidisciplinary network.  Martine Pennetier 1      4/17/2014 5:26:00 PM  
Data Managers - Pivotal role in documentation of care for people with bleeding disorders in the Australian Bleeding Disorders Database (ABDR)  Deirdre Tuck 1      4/17/2014 3:35:00 AM  
Causes of death in haemophilia patients in Argentina  Daniela Neme 1      4/8/2014 9:21:00 PM  
       




Most viewed poster for this congress
Poster: 1
Visits: 2508
Title: A WEB SITE TO IMPROVE MANAGEMENT OF PATIENTS WITH INHERITED BLEEDING DISORDERS IN THE EMERGENCY DEPARTMENT: RESULTS AT 2 YEARS
Authors: Annarita Tagliaferri ,
Centre: Centro di Riferimento Regionale per la cura dellEmofilia

Poster most viewed in this topic
Poster: 1
Visits: 2508
Title: A WEB SITE TO IMPROVE MANAGEMENT OF PATIENTS WITH INHERITED BLEEDING DISORDERS IN THE EMERGENCY DEPARTMENT: RESULTS AT 2 YEARS
Authors: Annarita Tagliaferri ,
Centre: Centro di Riferimento Regionale per la cura dellEmofilia


 








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