Prevalence of von Willebrand Disease in Patients with Heavy Menstrual Bleeding: An Indian Perspective
暂无分享,去创建一个
[1] R. Marwaha,et al. Inherited Bleeding Disorders in North Indian Children: 14 years’ Experience from a Tertiary Care Center , 2019, Indian Journal of Hematology and Blood Transfusion.
[2] S. O’Brien. Evaluation and management of heavy menstrual bleeding in adolescents: the role of the hematologist. , 2018, Hematology. American Society of Hematology. Education Program.
[3] Ruchika Sharma,et al. Advances in the diagnosis and treatment of Von Willebrand disease. , 2017, Blood.
[4] R. Tait,et al. The diagnosis and management of von Willebrand disease: a United Kingdom Haemophilia Centre Doctors Organization guideline approved by the British Committee for Standards in Haematology , 2014, British journal of haematology.
[5] A. V. D. Van Der Zee,et al. The prevalence of underlying bleeding disorders in patients with heavy menstrual bleeding with and without gynecologic abnormalities. , 2013, American journal of obstetrics and gynecology.
[6] A. Iorio,et al. Management of Inherited von Willebrand Disease in Italy: Results from the Retrospective Study on 1234 Patients , 2011, Seminars in thrombosis and hemostasis.
[7] P. Badenhorst,et al. Laboratory diagnosis and management of von Willebrand disease in South Africa. , 2011, Seminars in thrombosis and hemostasis.
[8] E. Duncan,et al. Diagnosis and Management of Adult Patients with von Willebrand Disease in South Australia , 2011, Seminars in thrombosis and hemostasis.
[9] M. Broder,et al. FIGO classification system (PALM‐COEIN) for causes of abnormal uterine bleeding in nongravid women of reproductive age , 2011, International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics.
[10] Sandip Kumar,et al. Prevalence and spectrum of von Willebrand disease in Eastern Uttar Pradesh. , 2010, Indian journal of pathology & microbiology.
[11] R. Saxena,et al. Spectrum of Von Willebrand disease and inherited platelet function disorders amongst Indian bleeders , 2007, Annals of Hematology.
[12] A. Johansson,et al. Genetic analysis of 31 Swedish type 1 von Willebrand disease families reveals incomplete linkage to the von Willebrand factor gene and a high frequency of a certain disease haplotype , 2005, Journal of thrombosis and haemostasis : JTH.
[13] Rajiv K. Saxena,et al. Relatively high frequency of VWD types 3 and 2 in a cohort of Indian patients: the role of multimeric analysis , 2005, Journal of thrombosis and haemostasis : JTH.
[14] D. Economides,et al. von Willebrand disease in women with menorrhagia: a systematic review , 2004, BJOG : an international journal of obstetrics and gynaecology.
[15] S. Perkins,et al. Identification of Type 2 von Willebrand Disease in Previously Diagnosed Type 1 Patients: a Reappraisal Using Phenotypes, Genotypes and Molecular Modelling , 2000, Thrombosis and Haemostasis.
[16] F. Howard,et al. Gynaecological and obstetrical morbidity in women with type I von Willebrand disease: results of a patient survey , 2000, Haemophilia : the official journal of the World Federation of Hemophilia.
[17] P. Mannucci,et al. Impact, Diagnosis and Treatment of von Willebrand Disease , 2000, Thrombosis and Haemostasis.
[18] Nilsson. Commentary to Erik von Willebrand’s original paper from 1926 ‘Hereditär pseudohemofili’ , 1999, Haemophilia : the official journal of the World Federation of Hemophilia.
[19] M. Howard,et al. Ristocetin - A New Tool in the Investigation of Platelet Aggregation , 1971, Thrombosis and Haemostasis.
[20] R. Saxena,et al. Inherited platelet function disorders versus other inherited bleeding disorders: an Indian overview. , 2008, Thrombosis research.
[21] T. Abshire. Prophylaxis and von Willebrand's disease (vWD). , 2006, Thrombosis research.
[22] D. Mohanty,et al. Spectrum of inherited bleeding disorders from Western India. , 2002, Haematologia.