
Rare Coagulation Disorders
The Rare Coagulation Disorders Resource Room (https://rarecoagulationdisorders.org/), a dynamic, open-access website, was developed through a collaboration of the international …
Rare Bleeding Disorders Database (RBDD)
The Rare Bleeding Disorders Database (RBDD) is a registry whose mission is to set up a network of treatment centers dealing with rare bleeding disorders (RBDs) with the goal of developing a …
RBDD rare bleeding disorders database - PRO-RBDD | RBDD rare …
PRO-RBDD is an international collaborating network that has developed a web database designed to prospectively collect clinical and laboratory data of patients with coagulation factor …
Minimal factor XIII activity level to prevent major ... - PubMed
Conclusion The PRO-RBDD study suggests a FXIII coagulant activity level of 15 IU dL -1 as a target to start prophylaxis in order to prevent major bleedings, such as central nervous system …
National and international registries of rare bleeding disorders
Rare bleeding disorders (RBDs) are autosomal recessive disorders, representing 3–5% of all the inherited deficiencies of coagulation factors. Their frequency in the general population ranges …
Rare Coagulation Resource Room | NBDF - bleeding.org
Explore the Rare Coagulation Resource Room, providing valuable information on rare bleeding disorders. Learn about basic science, clinical management & more.
Rare bleeding disorders: diagnosis and treatment - ScienceDirect
2015年3月26日 · Rare inherited bleeding disorders (RBDs), including deficiencies of coagulation factors fibrinogen, factor (F)II, FV, combined FV and FVIII, FVII, FX, FXI, FXIII, and congenital …
Resources - Rare Coagulation Disorders
Rare Coagulation Disorders Resource Room, an extension of the RBDD Registry (eu.rbdd.org), was developed in collaboration with the Indiana Hemophilia & Thrombosis Center …
Prospective Data Collection on Patients with Fibrinogen and Factor …
2014年12月6日 · The PRO-RBDD is a prospective study of fibrinogen and FXIII deficiency designed to collect data on demographics, laboratory phenotype, genotype, clinical …
Minimal factor XIII activity level to prevent major spontaneous …
2017年9月1日 · Congenital factor XIII (FXIII) deficiency is a rare bleeding disorder associated with significant bleeding manifestations. The European Network of Rare Bleeding Disorders …