Low‐dose prophylaxis for children with haemophilia in a resource‐limited setting in south India—A clinical audit report
暂无分享,去创建一个
R. Sudevan | N. Sidharthan | A. Sudhakar | V. Narayana Pillai | S. Mathew | M. Raj | D. Viswam | C. Joseph
[1] T. Dutta,et al. A randomized study of very low‐dose factor VIII prophylaxis in severe haemophilia – A success story from a resource limited country , 2016, Haemophilia : the official journal of the World Federation of Hemophilia.
[2] L. Valentino. Considerations in individualizing prophylaxis in patients with haemophilia A , 2014, Haemophilia : the official journal of the World Federation of Hemophilia.
[3] A. Gringeri,et al. The burden of bleeding in haemophilia: is one bleed too many? , 2014, Haemophilia : the official journal of the World Federation of Hemophilia.
[4] J. Korth-Bradley,et al. Factors that influence the bleeding phenotype in severe hemophilic patients , 2013, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.
[5] C. Kempton,et al. Randomized, controlled, parallel‐group trial of routine prophylaxis vs. on‐demand treatment with sucrose‐formulated recombinant factor VIII in adults with severe hemophilia A (SPINART) , 2013, Journal of thrombosis and haemostasis : JTH.
[6] J. Mahlangu,et al. Guidelines for the management of hemophilia , 2013, Haemophilia : the official journal of the World Federation of Hemophilia.
[7] M. Makris. Prophylaxis in haemophilia should be life-long. , 2012, Blood transfusion = Trasfusione del sangue.
[8] L. Mantovani,et al. A randomized clinical trial of prophylaxis in children with hemophilia A (the ESPRIT Study) , 2011, Journal of thrombosis and haemostasis : JTH.
[9] R. Engelbert,et al. Validation of a new pediatric joint scoring system from the International Hemophilia Prophylaxis Study Group: Validity of the hemophilia joint health score , 2011, Arthritis care & research.
[10] R. Wu,et al. Low dose secondary prophylaxis reduces joint bleeding in severe and moderate haemophilic children: a pilot study in China , 2011, Haemophilia : the official journal of the World Federation of Hemophilia.
[11] B. Coller,et al. ISTH/SSC bleeding assessment tool: a standardized questionnaire and a proposal for a new bleeding score for inherited bleeding disorders , 2010, Journal of thrombosis and haemostasis : JTH.
[12] B. George,et al. Polymorphism in factor VII gene modifies phenotype of severe haemophilia , 2009, Haemophilia : the official journal of the World Federation of Hemophilia.
[13] L. Valentino,et al. Optimizing outcomes for patients with severe haemophilia A , 2007, Haemophilia : the official journal of the World Federation of Hemophilia.
[14] Alan R. Cohen,et al. Prophylaxis versus episodic treatment to prevent joint disease in boys with severe hemophilia. , 2007, The New England journal of medicine.
[15] D. Grobbee,et al. Variability in clinical phenotype of severe haemophilia: the role of the first joint bleed , 2005, Haemophilia : the official journal of the World Federation of Hemophilia.
[16] J. Astermark,et al. Primary prophylaxis in severe haemophilia should be started at an early age but can be individualized , 1999, British journal of haematology.
[17] C. Kessler. ‘Dose requirement for replacement therapy in hemophilia A’ , 1997, Haemophilia : the official journal of the World Federation of Hemophilia.
[18] H. Pettersson,et al. Twenty‐five years' experience of prophylactic treatment in severe haemophilia A and B , 1992, Journal of internal medicine.
[19] N. Ciavarella,et al. Early treatment of hemophilia with minimal doses of factor VIII or factor IX. , 1978, Blood.