Prevalence of von Willebrand Disease in Patients with Heavy Menstrual Bleeding: An Indian Perspective

[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.