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WFH 2014 World Congress

 

11-15 May 2014 Melbourne
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Discussion forum - WFH 2014 World Congress
    Topic - Rare Congenital Bleeding Disorders

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 Thread / Poster  Author  Replies  Last reply
Congenital factor V deficiency, comparison the severity of clinical presentations among patients with rare bleeding disorders  Akbar Dorgalaleh 1      5/5/2014 6:49:00 AM  
Molecular analysis, Clinical Manifestations and Management of Factor XIII Deficiency in Southeast of Iran  Akbar Dorgalaleh 1      5/5/2014 6:30:00 AM  
Long term two central follow up study on a large group of patients with congenital factor XIII deficiency treated prophylactically with Fibrogammin P  Akbar Dorgalaleh 1      5/5/2014 6:25:00 AM  
Recurrent venous thromboembolic event in a sever factor X deficient patient without any correlation to Pro-coagulant product.  PEYMAN ESHGHI 1      5/5/2014 5:03:00 AM  
A case of factor X (FX) deficiency caused by novel mutations Q56K, Q104X  Jaewoo Song 1      4/23/2014 11:13:00 PM  
THROMBIN GENERATION OF PATIENTS WITH FACTOR XI DEFICIENCY  Le Quellec Sandra 1      4/23/2014 3:39:00 PM  
Rare factor deficiencies and circumcision:Cukurova Experience  Ilgen Sasmaz 1      4/23/2014 3:24:00 PM  
Prophylactic therapy with fibrinogen concentrate prevents recurrent pain episodes, but not radiological deterioration, in two cases having bone cysts as a rare complication of afibrinogenemia  Monique van Meegeren 1      4/23/2014 11:06:00 AM  
Congenital Coagulation Factor VII Deficiency: A Phenotype and Genotype Study in Taiwan  Yeu-Chin Chen 1      4/23/2014 6:19:00 AM  
Factor VII Deficiency Patients: 5 Years Factors Concentrates Utilization Trend based on the Canadian Hemophilia Assessment and Resource Management System (CHARMS)  Aicha TRAORE 1      4/22/2014 7:08:00 PM  
Factor XIII Deficiency As Underlying Cause Of Unexplained Bleeding  Marta Ruiz Mercado 1      4/22/2014 1:28:00 AM  
Vitamin K Prophylaxis In A Child Of Hereditary Combined Deficiency Of Vitamin K-Dependent Clotting Factors.  M. Soker 1      4/21/2014 8:54:00 PM  
A case of severe factor XIII deficiency with an unusual uniparental disomy heredity  Ming-Ching Shen 1      4/21/2014 1:15:00 PM  
Successful use of Recombinant Factor VIIa for menorrhagia control in a patient with Glanzmanns thrombasthenia  soeun Jun 1      4/21/2014 5:47:00 AM  
Update on Platelet-type Von Willebrand Disease Registry and Proposed Mechanisms for Newly Reported Mutations  Maha Othman 1      4/15/2014 2:19:00 AM  
Co-localization analysis of pathological FXIIIB subunit mutants confirm an indirect but varied effect on secretion.  Anne Thomas 1      4/14/2014 11:43:00 AM  
Defective ER retention signal due to mutation VKORC1:p.Arg98Trp results in VKCFD2  Katrin Jeannette Czogalla 1      4/9/2014 11:16:00 AM  
Assessment of bleeding phenotype in PT-VWD and other RBDs using electronic bleeding questionnaire (eBQ): a retrospective study on 55 subjects  Harmanpreet Kaur 1      4/7/2014 4:20:00 PM  
Major Surgical Interventions in Childhood Factor VII Deficiency  Zafer Salcioglu 1      4/3/2014 2:10:00 PM  
Effective management of surgical procedures of inherited FVII deficient patient six-year experience at University Hospital in Ostrava  Raquel Hernández Sánchez 1      3/19/2014 6:21:00 PM  
CONGENITAL FACTOR X DEFICIENCY ASSOCIATION BETWEEN COAGULANT FACTOR ACTIVITY AND CLINICAL BLEEDING SEVERITY IN FOUR CASES  Zahra Badiei 1      3/14/2014 6:30:00 PM  
Familial vitamin K clotting factor deficiencies (VKCFD) in an infant with novel mutation in Gamma-glutamyl carboxylase (GGCX) gene  Mrs.Nongnuch Sirachainan 1      3/13/2014 5:42:00 AM  
Development in the management of congenital factor XIII deficiency with factor XIII concentrate  Narges beigom Mirbehbahani 1      3/12/2014 12:30:00 PM  
       




Most viewed poster for this congress
Poster: 1
Visits: 2526
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: 4
Visits: 1569
Title: GGCX Splice-Site Mutations: Functional Investigation in a chimeric Minigene System
Authors: Matthias Watzka ,
Centre: Institute of Experimental Haematology and Transfusion Medicine, University Clinics Bonn, Germany


 








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