Diagnosis and management of acquired thrombotic thrombocytopenic purpura in southeast China: a single center experience of 60 cases
暂无分享,去创建一个
Jian Huang | Jie Jin | W. Qian | Xinping Zhou | C. Mei | Liya Ma | Wei-lai Xu | L. Ye | H. Tong | W. Mai | Juying Wei | H. Meng | X. Ye | Y. Ren
[1] E. Wood,et al. Diagnosis and management of thrombotic thrombocytopenic purpura (TTP) in Australia: findings from the first 5 years of the Australian TTP/thrombotic microangiopathy registry , 2016, Internal medicine journal.
[2] P. Coppo,et al. [Management of thrombotic thrombocytopenic purpura in two French centers: A series of 27 patients]. , 2016, La Revue de medecine interne.
[3] J. Sadler. What's new in the diagnosis and pathophysiology of thrombotic thrombocytopenic purpura. , 2015, Hematology. American Society of Hematology. Education Program.
[4] P. Coppo,et al. Treatment of thrombotic thrombocytopenic purpura beyond therapeutic plasma exchange. , 2015, Hematology. American Society of Hematology. Education Program.
[5] L. Ye,et al. Long-term remission induced by low-dose rituximab for relapsed and refractory thrombotic thrombocytopenic purpura: A report of two cases. , 2015, Experimental and therapeutic medicine.
[6] C. Abrams,et al. How I treat refractory thrombotic thrombocytopenic purpura. , 2015, Blood.
[7] S. Cataland,et al. Acquired thrombotic thrombocytopenic purpura: new therapeutic options and their optimal use , 2015, Journal of thrombosis and haemostasis : JTH.
[8] S. Vesely,et al. The role of rituximab in the management of patients with acquired thrombotic thrombocytopenic purpura. , 2015, Blood.
[9] L. Bouillet,et al. Prise en charge du purpura thrombotique thrombopénique dans deux centres français : à partir de 27 patients , 2015 .
[10] H. Ha,et al. Current status in diagnosis and treatment of hereditary thrombotic thrombocytopenic purpura. , 2015 .
[11] A. Barrett,et al. ST2: the biomarker at the heart of GVHD severity. , 2015, Blood.
[12] H. Hanby,et al. Current status in diagnosis and treatment of hereditary thrombotic thrombocytopenic purpura. , 2014, Hereditary genetics : current research.
[13] F. Peyvandi,et al. Guidelines on the diagnosis and management of thrombotic thrombocytopenic purpura and other thrombotic microangiopathies , 2012, British journal of haematology.
[14] B. Myers. Diagnosis and management of maternal thrombocytopenia in pregnancy , 2012, British journal of haematology.
[15] J. Holz. The TITAN trial--assessing the efficacy and safety of an anti-von Willebrand factor Nanobody in patients with acquired thrombotic thrombocytopenic purpura. , 2012, Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis.
[16] H. Kwaan,et al. Gain-of-function ADAMTS13 variants that are resistant to autoantibodies against ADAMTS13 in patients with acquired thrombotic thrombocytopenic purpura. , 2012, Blood.
[17] K. Nollet. Future outlook in transfusion therapy. , 2012, Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis.
[18] S. Held,et al. Novel treatment concepts for graft-versus-host disease. , 2012, Blood.
[19] [Consensus of Chinese experts on diagnosis and treatment of thrombotic thrombocytopenic purpura (version 2012)]. , 2012, Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi.
[20] J. Voorberg,et al. Essential Domains of A Disintegrin and Metalloprotease With Thrombospondin Type 1 Repeats-13 Metalloprotease Required for Modulation of Arterial Thrombosis , 2011, Arteriosclerosis, thrombosis, and vascular biology.
[21] H. Ehrlich,et al. Recombinant ADAMTS13 normalizes von Willebrand factor‐cleaving activity in plasma of acquired TTP patients by overriding inhibitory antibodies , 2011, Journal of Thrombosis and Haemostasis.
[22] D. Varon,et al. Development, Cell Differentiation, Angiogenesis—Microparticles and Their Roles in Angiogenesis , 2011, Arteriosclerosis, thrombosis, and vascular biology.
[23] J. Segal,et al. Thrombotic thrombocytopenic purpura at the Johns Hopkins Hospital from 1992 to 2008: clinical outcomes and risk factors for relapse , 2010, Transfusion.
[24] M. Scully,et al. Human leukocyte antigen association in idiopathic thrombotic thrombocytopenic purpura: evidence for an immunogenetic link , 2010, Journal of thrombosis and haemostasis : JTH.
[25] C. Esmon. The discovery of the endothelial cell protein C receptor , 2010, Journal of thrombosis and haemostasis : JTH.
[26] Ian Mackie,et al. Regional UK TTP Registry: correlation with laboratory ADAMTS 13 analysis and clinical features , 2008, British journal of haematology.
[27] J. Plate. Signals that maintain leukemic cell viability. , 2008, Blood.
[28] J. Sadler. Von Willebrand factor, ADAMTS13, and thrombotic thrombocytopenic purpura. , 2008, Blood.
[29] A. Chauhan,et al. Systemic antithrombotic effects of ADAMTS13 , 2006, The Journal of experimental medicine.
[30] Heather L. Van Epps. Editing HIV to death , 2006 .
[31] S. Vesely,et al. The incidence of thrombotic thrombocytopenic purpura‐hemolytic uremic syndrome: all patients, idiopathic patients, and patients with severe ADAMTS‐13 deficiency , 2005, Journal of thrombosis and haemostasis : JTH.
[32] U. Schoepf,et al. Spiral computed tomography is the first‐line chest imaging test for acute pulmonary embolism: yes , 2005, Journal of thrombosis and haemostasis : JTH.
[33] 王兆钺,et al. Evaluation of von Willebrand factor-cleaving protease activity in patients with thrombotic thrombocytopenic purpura , 2004 .
[34] O. Van den Bergh,et al. Medically unexplained dyspnea: psychophysiological characteristics and role of breathing therapy. , 2004, Chinese medical journal.
[35] J. Moake,et al. Recent advances in thrombotic thrombocytopenic purpura. , 2004, Hematology. American Society of Hematology. Education Program.
[36] D. Higgs. Gene regulation in hematopoiesis: new lessons from thalassemia. , 2004, Hematology. American Society of Hematology. Education Program.
[37] K. Fujikawa,et al. Structure of von Willebrand Factor-cleaving Protease (ADAMTS13), a Metalloprotease Involved in Thrombotic Thrombocytopenic Purpura* , 2001, The Journal of Biological Chemistry.