Management of rare coagulation disorders in 2018.
暂无分享,去创建一个
[1] É. Katona,et al. Auto‐ and alloantibodies against factor XIII: laboratory diagnosis and clinical consequences , 2018, Journal of thrombosis and haemostasis : JTH.
[2] Esther S. Kim,et al. Emicizumab-kxwh: First Global Approval , 2018, Drugs.
[3] M. Franchini,et al. Inhibitors in Patients with Congenital Bleeding Disorders Other Than Hemophilia , 2017, Seminars in Thrombosis and Hemostasis.
[4] G. Kenet,et al. Primary prophylaxis for children with severe congenital factor VII deficiency - Clinical and laboratory assessment. , 2017, Blood cells, molecules & diseases.
[5] J. Oldenburg,et al. Emicizumab Prophylaxis in Hemophilia A with Inhibitors , 2017, The New England journal of medicine.
[6] A. Akinc,et al. Targeting of Antithrombin in Hemophilia A or B with RNAi Therapy , 2017, The New England journal of medicine.
[7] H. Li,et al. Genetic diagnosis in Hemophilia A from southern China: five novel mutations and one preimplantation genetic analysis , 2017, International journal of laboratory hematology.
[8] G. Castaman,et al. Diagnosis and Treatment of von Willebrand Disease and Rare Bleeding Disorders , 2017, Journal of clinical medicine.
[9] J. Huntington,et al. Design and characterization of an APC-specific serpin for the treatment of hemophilia. , 2017, Blood.
[10] B. Kerlin,et al. Developing the First Recombinant Factor XIII for Congenital Factor XIII Deficiency: Clinical Challenges and Successes , 2016, Seminars in Thrombosis and Hemostasis.
[11] F. Peyvandi,et al. Establishment of a bleeding score as a diagnostic tool for patients with rare bleeding disorders. , 2016, Thrombosis research.
[12] J. Peterson,et al. Targeting TFPI for hemophilia treatment. , 2016, Thrombosis research.
[13] A. Shirdel,et al. Desmopressin acetate as a haemostatic elevator in individuals with combined deficiency of factors V and VIII: a clinical trial , 2016, Journal of thrombosis and haemostasis : JTH.
[14] R. Kulkarni. Improving care and treatment options for women and girls with bleeding disorders , 2015, European journal of haematology.
[15] U. Martinowitz,et al. The impact of thrombin generation and rotation thromboelastometry on assessment of severity of factor XI deficiency. , 2015, Thrombosis research.
[16] S. Borrego,et al. Experience of Preimplantation Genetic Diagnosis for Hemophilia at the University Hospital Virgen Del Rocío in Spain: Technical and Clinical Overview , 2015, BioMed research international.
[17] M. Borhany,et al. A new report of FVII‐inhibitor in a patient suffering from severe congenital FVII deficiency , 2015, Haemophilia : the official journal of the World Federation of Hemophilia.
[18] S. Milstein,et al. An RNAi therapeutic targeting antithrombin to rebalance the coagulation system and promote hemostasis in hemophilia , 2015, Nature Medicine.
[19] S. Lethagen,et al. Safety and pharmacokinetics of anti‐TFPI antibody (concizumab) in healthy volunteers and patients with hemophilia: a randomized first human dose trial , 2015, Journal of thrombosis and haemostasis : JTH.
[20] A. Shapiro,et al. Rare bleeding disorders: diagnosis and treatment. , 2015, Blood.
[21] A. Mangione,et al. Pharmacokinetics and safety of plasma‐derived factor XIII concentrate (human) in patients with congenital factor XIII deficiency , 2015, Haemophilia : the official journal of the World Federation of Hemophilia.
[22] M. Callaghan,et al. Thromboelastography identifies children with rare bleeding disorders and predicts bleeding phenotype , 2015, Haemophilia : the official journal of the World Federation of Hemophilia.
[23] A. Mangione,et al. Efficacy and safety of prophylactic treatment with plasma‐derived factor XIII concentrate (human) in patients with congenital factor XIII deficiency , 2015, Haemophilia : the official journal of the World Federation of Hemophilia.
[24] F. Peyvandi,et al. Comparison of Thrombin Generation Assay With Conventional Coagulation Tests in Evaluation of Bleeding Risk in Patients With Rare Bleeding Disorders , 2014, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.
[25] A. Mumford,et al. Guideline for the diagnosis and management of the rare coagulation disorders , 2014, British journal of haematology.
[26] S. Lukowski,et al. FGB mutations leading to congenital quantitative fibrinogen deficiencies: an update and report of four novel mutations. , 2014, Thrombosis research.
[27] S. Borrego,et al. Experience of Preimplantation Genetic Diagnosis with HLA Matching at the University Hospital Virgen del Rocío in Spain: Technical and Clinical Overview , 2014, BioMed research international.
[28] G. Mariani,et al. Inhibitors to factor VII in congenital factor VII deficiency , 2014, Haemophilia : the official journal of the World Federation of Hemophilia.
[29] J. Griffin,et al. Improved hemostasis in hemophilia mice by means of an engineered factor Va mutant , 2014, Journal of thrombosis and haemostasis : JTH.
[30] F. Peyvandi,et al. Genetic sequence analysis of inherited bleeding diseases. , 2013, Blood.
[31] F. Peyvandi,et al. Rare Bleeding Disorders: Worldwide Efforts for Classification, Diagnosis, and Management , 2013, Seminars in Thrombosis & Hemostasis.
[32] Bin Zhang,et al. Combined Deficiency of Coagulation Factors V and VIII: An Update , 2013, Seminars in Thrombosis & Hemostasis.
[33] A. Chuansumrit,et al. Prophylaxis in congenital factor VII deficiency: indications, efficacy and safety. Results from the Seven Treatment Evaluation Registry (STER) , 2013, Haematologica.
[34] R. Pruthi,et al. Successful treatment with thalidomide of a patient with congenital factor V deficiency and factor V inhibitor with recurrent gastrointestinal bleeding from small bowel arteriovenous malformations , 2013, Haemophilia : the official journal of the World Federation of Hemophilia.
[35] G. Rodgers. Prothrombin complex concentrates in emergency bleeding disorders , 2012, American journal of hematology.
[36] F. Peyvandi,et al. Classification of rare bleeding disorders (RBDs) based on the association between coagulant factor activity and clinical bleeding severity , 2012, Journal of thrombosis and haemostasis : JTH.
[37] A. Rivkind,et al. Recombinant factor VIIa treatment for asymptomatic factor VII deficient patients going through major surgery , 2012, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.
[38] B. George,et al. Correlating clinical manifestations with factor levels in rare bleeding disorders: a report from Southern India , 2012, Haemophilia : the official journal of the World Federation of Hemophilia.
[39] G. Barillari,et al. Whole blood rotation thromboelastometry (ROTEM®) in nine severe factor V deficient patients and evaluation of the role of intraplatelets factor V , 2012, Haemophilia : the official journal of the World Federation of Hemophilia.
[40] F. Rosendaal,et al. Coagulation factor activity and clinical bleeding severity in rare bleeding disorders: results from the European Network of Rare Bleeding Disorders , 2012, Journal of thrombosis and haemostasis : JTH.
[41] Christine A. Lee,et al. Evaluation and management of acute menorrhagia in women with and without underlying bleeding disorders: consensus from an international expert panel. , 2011, European journal of obstetrics, gynecology, and reproductive biology.
[42] E. Tuddenham,et al. Monitoring low dose recombinant factor VIIa therapy in patients with severe factor XI deficiency undergoing surgery , 2011, Thrombosis and Haemostasis.
[43] F. Peyvandi,et al. Prenatal diagnosis and preimplantation genetic diagnosis: novel technologies and state of the art of PGD in different regions of the world , 2011, Haemophilia : the official journal of the World Federation of Hemophilia.
[44] G. Pike,et al. Factor deficiencies in pregnancy. , 2011, Hematology/oncology clinics of North America.
[45] M. Borhany,et al. Bleeding disorders in the tribe: result of consanguineous in breeding , 2010, Orphanet journal of rare diseases.
[46] P. de Mazancourt,et al. Thrombin generation in patients with factor XI deficiency and clinical bleeding risk , 2010, Haemophilia : the official journal of the World Federation of Hemophilia.
[47] M. El Sayed Zaki,et al. Descriptive Epidemiology of Hemophilia and Other Coagulation Disorders in Mansoura, Egypt: Retrospective Analysis. , 2010, Mediterranean journal of hematology and infectious diseases.
[48] G. Mariani,et al. Hereditary combined deficiency of the vitamin K-dependent clotting factors , 2010, Orphanet journal of rare diseases.
[49] A. James,et al. Women and bleeding disorders , 2010, Haemophilia : the official journal of the World Federation of Hemophilia.
[50] D. Perry,et al. A review of long‐term prophylaxis in the rare inherited coagulation factor deficiencies , 2009, Haemophilia : the official journal of the World Federation of Hemophilia.
[51] G. Kenet,et al. Lower doses of rFVIIa therapy are safe and effective for surgical interventions in patients with severe FXI deficiency and inhibitors , 2009, Haemophilia : the official journal of the World Federation of Hemophilia.
[52] I. Jaouad,et al. Consanguineous marriages in Morocco and the consequence for the incidence of autosomal recessive disorders. , 2009, Journal of biosocial science.
[53] U. Seligsohn,et al. Recombinant activated factor VII and tranexamic acid are haemostatically effective during major surgery in factor XI-deficient patients with inhibitor antibodies , 2009, Thrombosis and Haemostasis.
[54] A. Memon,et al. Hereditary prothrombin deficiency. , 2009, JPMA. The Journal of the Pakistan Medical Association.
[55] U. Seligsohn. Factor XI deficiency in humans , 2009, Journal of thrombosis and haemostasis : JTH.
[56] P. Mannucci,et al. Introduction: Rare Bleeding Disorders: General Aspects of Clinical Features, Diagnosis, and Management , 2009, Seminars in thrombosis and hemostasis.
[57] G. Mariani,et al. Factor VII Deficiency , 2009, Seminars in thrombosis and hemostasis.
[58] P. de Moerloose,et al. Congenital Fibrinogen Disorders , 2009, Seminars in thrombosis and hemostasis.
[59] J. Oldenburg,et al. Vitamin K–Dependent Coagulation Factors Deficiency , 2009, Seminars in thrombosis and hemostasis.
[60] F. Peyvandi,et al. Combined Factor V and Factor VIII Deficiency. , 2009, Seminars in Thrombosis and Hemostasis.
[61] P. Bolton-Maggs. Factor XI deficiency--resolving the enigma? , 2009, Hematology. American Society of Hematology. Education Program.
[62] S. Acharya,et al. Rare inherited disorders of fibrinogen , 2008, Haemophilia : the official journal of the World Federation of Hemophilia.
[63] G. Mariani,et al. Factor VII deficiency: defining the clinical picture and optimizing therapeutic options , 2008, Haemophilia : the official journal of the World Federation of Hemophilia.
[64] P. Monahan,et al. Familial deficiency of vitamin K‐dependent clotting factors , 2008, Haemophilia : the official journal of the World Federation of Hemophilia.
[65] F. Peyvandi,et al. National and international registries of rare bleeding disorders. , 2008, Blood transfusion = Trasfusione del sangue.
[66] S. Adil,et al. Frequency and clinical spectrum of rare inherited coagulopathies--a tricenter study. , 2008, JPMA. The Journal of the Pakistan Medical Association.
[67] G. Davı̀,et al. Inherited bleeding disorders: results from the Italian Regional Haemophilia Centre of Pescara. , 2008, Blood transfusion = Trasfusione del sangue.
[68] M. Marietta,et al. A web‐based registry of inherited bleeding disorders in the region of Emilia‐Romagna: results at three and a half years , 2008, Haemophilia : the official journal of the World Federation of Hemophilia.
[69] A. Girolami,et al. Congenital FX deficiency combined with other clotting defects or with other abnormalities: a critical evaluation of the literature , 2008, Haemophilia : the official journal of the World Federation of Hemophilia.
[70] M. Makris,et al. Blood product support for delivery in severe factor X deficiency: the use of thrombin generation to guide therapy. , 2007, Blood transfusion = Trasfusione del sangue.
[71] 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.
[72] S. Pavord,et al. The obstetric and gynaecological management of women with inherited bleeding disorders – review with guidelines produced by a taskforce of UK Haemophilia Centre Doctors’ Organization , 2006, Haemophilia : the official journal of the World Federation of Hemophilia.
[73] P. Mannucci,et al. Genetic diagnosis of haemophilia and other inherited bleeding disorders , 2006, Haemophilia : the official journal of the World Federation of Hemophilia.
[74] P. Monagle,et al. Developmental haemostasis , 2006, Thrombosis and Haemostasis.
[75] U. Seligsohn,et al. Inhibitors to Factor XI in patients with severe Factor XI deficiency. , 2006, Seminars in hematology.
[76] K. Wulff,et al. Influence of Factor V HR2 on Thrombin Generation and Clinical Manifestation in Rare Bleeding Disorders , 2006, Pathophysiology of Haemostasis and Thrombosis.
[77] Deborah L Brown. Congenital bleeding disorders. , 2005, Current problems in pediatric and adolescent health care.
[78] P. Mannucci,et al. Recessively inherited coagulation disorders. , 2004, Blood.
[79] M. Saadat,et al. Short ReportConsanguineous marriage in Iran , 2004, Annals of human biology.
[80] D. Dimichele,et al. Rare Bleeding Disorder Registry: deficiencies of factors II, V, VII, X, XIII, fibrinogen and dysfibrinogenemias , 2004, Journal of Thrombosis and Haemostasis.
[81] D. Steinberg,et al. Inherited factor XI deficiency confers no protection against acute myocardial infarction , 2003, Journal of thrombosis and haemostasis : JTH.
[82] L. Muszbek,et al. Coagulation Factor Deficiencies and Pregnancy Loss , 2003, Seminars in thrombosis and hemostasis.
[83] C. Hermans,et al. Successful use of recombinant factor VIIa in a patient with inhibitor secondary to severe factor XI deficiency , 2002, Haemophilia : the official journal of the World Federation of Hemophilia.
[84] J. Abgrall,et al. The use of recombinant factor VIIa (NovoSeven) in a patient with a factor XI deficiency and a circulating anticoagulant. , 2001, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.
[85] M. Koh,et al. Factor V inhibitor in neonatal intracranial hemorrhage secondary to severe congenital factor V deficiency. , 2001, Journal of pediatric hematology/oncology.
[86] J. Abgrall,et al. [Factor XI inhibitors : clinical and biological features]. , 2001, Annales de biologie clinique.
[87] Bolton‐Maggs. Factor XI deficiency and its management , 2000, Haemophilia : the official journal of the World Federation of Hemophilia.
[88] S. Antonarakis,et al. Mutations in the fibrinogen aalpha gene account for the majority of cases of congenital afibrinogenemia. , 2000, Blood.
[89] F. Rosendaal,et al. High levels of coagulation factor XI as a risk factor for venous thrombosis. , 2000, The New England journal of medicine.
[90] Hann,et al. Severe factor V deficiency and neonatal intracranial haemorrhage: a case report , 2000, Haemophilia : the official journal of the World Federation of Hemophilia.
[91] P. Mannucci,et al. Bleeding and thrombosis in 55 patients with inherited afibrinogenaemia , 1999, British journal of haematology.
[92] F. Peyvandi,et al. Symptoms of inherited factor V deficiency in 35 Iranian patients , 1998, British journal of haematology.
[93] Mannucci,et al. Bleeding symptoms in 27 Iranian patients with the combined deficiency of factor V and factor VIII , 1998, British journal of haematology.
[94] A. Bener,et al. CONSANGUINEOUS MARRIAGES IN THE UNITED ARAB EMIRATES , 1997, Journal of Biosocial Science.
[95] M. Mittelman,et al. The two common mutations causing factor XI deficiency in Jews stem from distinct founders: one of ancient Middle Eastern origin and another of more recent European origin. , 1997, Blood.
[96] Muneera Al Bunyan,et al. Consanguineous marriages in a Saudi population and the effect of inbreeding on prenatal and postnatal mortality , 1997 .
[97] M. Andrew,et al. The relevance of developmental hemostasis to hemorrhagic disorders of newborns. , 1997, Seminars in perinatology.
[98] M. Samama,et al. Familial Dysfibrinogenemia and Thrombophilia , 1995, Thrombosis and Haemostasis.
[99] E. Davie,et al. Factor XI deficiency in Ashkenazi Jews in Israel. , 1991, The New England journal of medicine.
[100] G. Mariani,et al. Inhibitor to factor V in severe factor V congenital deficiency. A case report. , 1985, Nouvelle revue francaise d'hematologie.
[101] H. El-Tahan,et al. Consanguineous matings in the Egyptian population. , 1983, Journal of medical genetics.