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WFH 2016 World Congress

24-28 July 2016 Orlando

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Discussion forum - WFH 2016 World Congress Topic - Databases & Registries If you are already registered in PosterSessionOnline, enter your e-mail and click on LOGIN. Otherwise click on REGISTER

Thread / Poster	Author	Replies	Last reply

Korea Hemophilia Foundation registry trends 1991-2014: patient registry, demographics, health services utilization	Soon Ki Kim Soon Ki Kim	1	7/8/2016 5:44:00 AM


A cross-sectional study of females with congenital bleeding disorders enrolled in the ATHNdataset	Kristina Haley	1	7/7/2016 10:04:00 PM


Joint Outcomes in United States (US) Hemophilia Patients: A Report of the Community Counts Registry	Marilyn Manco-Johnson	1	7/7/2016 7:29:00 PM


Comparison of parameters collected from clinical trials (performed in the frame of Marketing Authorization) and registries in severe Hemophilia A patients - A methodological exercise	Carla Jonker	1	7/7/2016 11:38:00 AM


Can the use of data derived from different data sources improve regulatory procedures in a rare disease like Hemophilia A?	Christine Keipert	1	7/7/2016 9:23:00 AM


Inherited bleeding disorders - experience of a not-for-profit organization in Pakistan	Shabneez Hussain	1	7/5/2016 1:03:00 PM


Most viewed poster for this congress

Poster: 13
Visits: 590
Title: Algorithmic evidence-based phenotype screening and collaborative approach to attacking symptoms of nonadherence in patients with bleeding disorders
Authors: Jay Bryant-Wimp , Jay Bryant-Wimp, RPh
Centre: Integrite Solutions


Poster most viewed in this topic

Poster: 31
Visits: 64
Title: Can the use of data derived from different data sources improve regulatory procedures in a rare disease like Hemophilia A?
Authors: Christine Keipert , Christine KeipertCarla J. JonkerH. Marijke van den BergAnneliese Hilger
Centre: Paul-Ehrlich-Institut

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