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WFH 2016 World Congress
24-28 July 2016 Orlando
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Discussion forum -
WFH 2016 World Congress
Topic -
Genetics of bleeding disorders
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Thread / Poster
Author
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Last reply
An unexpected finding: two different coagulation factor VIII gene mutations in brothers
Michael Steiner
1
7/20/2016 9:05:00 PM
Development of a lead candidate for Baxaltas AAV8-based FVIII gene therapy program BAX 888
Werner Hoellriegl
1
7/18/2016 12:25:00 PM
Genetic variant analysis in children and adults with hemophilia: experience from a large hemophilia center in the US
Jennifer Lemons
1
7/16/2016 8:24:00 PM
Preliminary Results of a Phase 1/2 Trial of SPK-9001, a Hyperactive FIX Variant Delievered by a Novel Capsid, Demonstrate Safety and Efficacy at the Lowest Dose Cohort
Alvin Luk
1
7/15/2016 2:05:00 AM
Complexities and resolution of gene variant interpretation in two hemophilia cases
Stefanie Dugan
1
7/7/2016 7:09:00 PM
Discrepancy of F8 and F9 gene variant classifications between clinical laboratories
Michelle Alabek
1
7/7/2016 12:07:00 PM
Exploring the causes of skewed X-chromosome inactivation: XIST genetic analysis of cases and controls
Claudia Pamela
1
7/6/2016 8:35:00 PM
Next Generation DNA sequencing for haemostatic and platelet disorders
Anne Goodeve
1
7/6/2016 4:12:00 PM
Factor VIII Gene Mutation and Hemophilic Arthropathy in Hemophilia A Patients
Tsung-Ying Li
1
7/6/2016 10:42:00 AM
Polygenic score analysis to find genetic factors of inhibitor development in Korean severe hemophilia A patients using WES
Hee Jo
1
7/6/2016 9:23:00 AM
Messenger RNA Analysis and Multiplex Ligation Probe Amplification for Hemophilia A Patients without Found Mutation or Suspected Exon(s) Deletion in Genomic DNA
Yeu-Chin Chen
1
6/29/2016 2:59:00 AM
Systematic molecular analysis in Hemophilia A patients in a cohort from Bogotá, Colombia
Luz Yunis
1
6/25/2016 11:13:00 PM
National prevalence of F8 gene intron 1 and 22 inversions and development of inhibitors to factor VIII in Mexican severe hemophilia A patients
Jose Angel
1
6/25/2016 2:14:00 AM
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:
29
Visits:
238
Title:
Next Generation DNA sequencing for haemostatic and platelet disorders
Authors:
Anne Goodeve , Nick Beauchamp, Laura Crookes, Nikolas Niksic
Centre:
Sheffield Childrens NHS Foundation Trust
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