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  1. 1
    An influence of ABO blood group on the rate of proteolysis of von Willebrand factor by ADAMTS13

    An influence of ABO blood group on the rate of proteolysis of von Willebrand factor by ADAMTS13 Autor D. J. Bowen

    Vydáno 2003
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  2. 2
    Von Willebrand Factor, ADAMTS13 and D-Dimer Are Correlated with Different Levels of Nephropathy in Type 1 Diabetes Mellitus

    Von Willebrand Factor, ADAMTS13 and D-Dimer Are Correlated with Different Levels of Nephropathy in Type 1 Diabetes Mellitus Autor Caroline Pereira Domingueti, Luci Maria Sant’Ana Dusse, Rodrigo Bastos Fóscolo, Janice Sepúlveda Reis, Joyce Maria Annichino‐Bizzacchi, Fernanda Andrade Orsi, Bruna de Moraes Mazetto, María das Graças Carvalho Ferriani, Karina Braga Gomes, Ana Paula Fernandes

    Vydáno 2015
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  3. 3
    A Novel Quantitative Hemolytic Assay Coupled with Restriction Fragment Length Polymorphisms Analysis Enabled Early Diagnosis of Atypical Hemolytic Uremic Syndrome and Identified Unique Predisposing Mutations in Japan

    A Novel Quantitative Hemolytic Assay Coupled with Restriction Fragment Length Polymorphisms Analysis Enabled Early Diagnosis of Atypical Hemolytic Uremic Syndrome and Identified Un... Autor Yoko Yoshida, Toshiyuki Miyata, Masanori Matsumoto, Hiroko Shirotani-Ikejima, Yumiko Uchida, Yoshifumi Ohyama, Tetsuro Kokubo, Yoshihiro Fujimura

    Vydáno 2015
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  4. 4
    Two Mechanistic Pathways for Thienopyridine-Associated Thrombotic Thrombocytopenic Purpura

    Two Mechanistic Pathways for Thienopyridine-Associated Thrombotic Thrombocytopenic Purpura Autor Charles L. Bennett, Benjamin Kim, Anaadriana Zakarija, Nicholas Bandarenko, Dilip K. Pandey, Charlie G. Buffie, June M. McKoy, A. Tevar, John Cursio, Paul R. Yarnold, Hau C. Kwaan, Davide De Masi, Ravi Sarode, Thomas J. Raife, Joseph E. Kiss, Dennis W. Raisch, Charles J. Davidson, J. Evan Sadler, Thomas L. Ortel, X. Long Zheng, Seiji Kato, Masanori Matsumoto, Masahito Uemura, Yoshihiro Fujimura

    Vydáno 2007
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  5. 5
    Natural history of Upshaw–Schulman syndrome based on ADAMTS13 gene analysis in Japan

    Natural history of Upshaw–Schulman syndrome based on ADAMTS13 gene analysis in Japan Autor Yoshihiro Fujimura, Masanori Matsumoto, Ayami Isonishi, Hideo Yagi, Koichi Kokame, Kenji Soejima, Mitsuru Murata, Toshiyuki Miyata

    Vydáno 2011
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  6. 6
    Interaction of the cysteine‐rich domain of snake venom metalloproteinases with the A1 domain of von Willebrand factor promotes site‐specific proteolysis of von Willebrand factor and inhibition of von Willebrand factor‐mediated platelet aggregation

    Interaction of the cysteine‐rich domain of snake venom metalloproteinases with the A1 domain of von Willebrand factor promotes site‐specific proteolysis of von Willebrand factor an... Autor Solange M.T. Serrano, Deyu Wang, John D. Shannon, Antônio F. M. Pinto, Renata Polanowska‐Grabowska, Jay W. Fox

    Vydáno 2007
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  7. 7
    von Willebrand factor fibers promote cancer-associated platelet aggregation in malignant melanoma of mice and humans

    von Willebrand factor fibers promote cancer-associated platelet aggregation in malignant melanoma of mice and humans Autor Alexander T. Bauer, Jan Suckau, K Frank, Anna Desch, Lukas Goertz, Andreas H. Wagner, Markus Hecker, Tobias Goerge, Ludmila Umansky, Philipp Beckhove, Jochen Utikal, Christian Gorzelanny, Nancy Díaz‐Valdés, Viktor Umansky, Stefan W. Schneider

    Vydáno 2015
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  8. 8
    Recombinant ADAMTS13 normalizes von Willebrand factor‐cleaving activity in plasma of acquired TTP patients by overriding inhibitory antibodies

    Recombinant ADAMTS13 normalizes von Willebrand factor‐cleaving activity in plasma of acquired TTP patients by overriding inhibitory antibodies Autor Barbara Plaimauer, Johanna A. Kremer Hovinga, Claudia Juno, Martin J. Wolfsegger, Susanna Skalicky, Michaela Schmidt, Leopold Grillberger, Meinhard Hasslacher, Paul Knöbl, Hartmut J. Ehrlich, Friedrich Scheiflinger

    Vydáno 2011
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  9. 9
    Factors Related to Thrombotic Microangiopathies in Pregnancy: Integrative Review

    Factors Related to Thrombotic Microangiopathies in Pregnancy: Integrative Review Autor Francisco Fábio Rodrigues. Gomes, Kelsen dos Santos. Sales, Antônio Fernandes Filho, Elaine Maria Leite Rangel Andrade, Paula Christianne Gomes Gouveia Souto Maia, Anne Milane Formiga Bezerra, Kévia Katiúcia Santos Bezerra, Maria Soraya Pereira Franco Adriano

    Vydáno 2015
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  10. 10
    Hemostatic Parameters according to Renal Function and Time after Transplantation in Brazilian Renal Transplanted Patients

    Hemostatic Parameters according to Renal Function and Time after Transplantation in Brazilian Renal Transplanted Patients Autor Ana Paula Lucas Mota, Patrícia Nessralla Alpoim, Roberta Carvalho de Figueiredo, Ana Cristina Simões e Silva, Karina Braga Gomes, Luci Maria Sant’Ana Dusse

    Vydáno 2015
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  11. 11
    ADAMTS13 reduces VWF‐mediated acute inflammation following focal cerebral ischemia in mice

    ADAMTS13 reduces VWF‐mediated acute inflammation following focal cerebral ischemia in mice Autor Mohammad Moshahid Khan, David G. Motto, Steven R. Lentz, Anil K. Chauhan

    Vydáno 2012
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  12. 12
    Pathogenicity of Anti-ADAMTS13 Autoantibodies in Acquired Thrombotic Thrombocytopenic Purpura

    Pathogenicity of Anti-ADAMTS13 Autoantibodies in Acquired Thrombotic Thrombocytopenic Purpura Autor Mari Thomas, Rens de Groot, Marie Scully, James T. B. Crawley

    Vydáno 2015
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  13. 13
    Decreasing frequency of plasma exchange complications in patients treated for thrombotic thrombocytopenic purpura‐hemolytic uremic syndrome, 1996 to 2011 (CME)

    Decreasing frequency of plasma exchange complications in patients treated for thrombotic thrombocytopenic purpura‐hemolytic uremic syndrome, 1996 to 2011 (CME) Autor Sumit Som, Cassandra C. Deford, Mandi L. Kaiser, Deirdra R. Terrell, Johanna A. Kremer Hovinga, Bernhard Lämmle, James N. George, Sara K. Vesely

    Vydáno 2012
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  14. 14
    Diagnosis and management of thrombotic thrombocytopenic purpura (TTP) in Australia: findings from the first 5 years of the Australian TTP/thrombotic microangiopathy registry

    Diagnosis and management of thrombotic thrombocytopenic purpura (TTP) in Australia: findings from the first 5 years of the Australian TTP/thrombotic microangiopathy registry Autor Piers Blombery, L. Kivivali, Dominic Pepperell, Zoe McQuilten, Sunelle Engelbrecht, Mark N. Polizzotto, Louise Phillips, Erica M. Wood, S. Cohney

    Vydáno 2015
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  15. 15
    High-resolution epitope mapping by HX MS reveals the pathogenic mechanism and a possible therapy for autoimmune TTP syndrome

    High-resolution epitope mapping by HX MS reveals the pathogenic mechanism and a possible therapy for autoimmune TTP syndrome Autor Veronica C. Casina, Wenbing Hu, Jian‐Hua Mao, Ruinan Lu, Hayley A. Hanby, Brandy Pickens, Zhong-Yuan Kan, Woon Ki Lim, Leland Mayne, Eric Ostertag, Stephen Kacir, Don L. Siegel, S. Walter Englander, X. Long Zheng

    Vydáno 2015
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  16. 16
    Impact of severe ADAMTS13 deficiency on clinical presentation and outcomes in patients with thrombotic microangiopathies: the experience of the Harvard TMA Research Collaborative

    Impact of severe ADAMTS13 deficiency on clinical presentation and outcomes in patients with thrombotic microangiopathies: the experience of the Harvard TMA Research Collaborative Autor Pavan K. Bendapudi, Ang Li, Ayad Hamdan, Lynne Uhl, Richard M. Kaufman, Christopher P. Stowell, Sunny Dzik, Robert S. Makar

    Vydáno 2015
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  17. 17
    Pathological von Willebrand factor fibers resist tissue plasminogen activator and ADAMTS13 while promoting the contact pathway and shear‐induced platelet activation

    Pathological von Willebrand factor fibers resist tissue plasminogen activator and ADAMTS13 while promoting the contact pathway and shear‐induced platelet activation Autor B.A. Herbig, Scott L. Diamond

    Vydáno 2015
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  18. 18
    Visualization of an N-terminal fragment of von Willebrand factor in complex with factor VIII

    Visualization of an N-terminal fragment of von Willebrand factor in complex with factor VIII Autor Andrew Yee, Austin N. Oleskie, Anne M. Dosey, Colin A. Kretz, Robert Gildersleeve, Somnath Dutta, Min Su, David Ginsburg, Georgios Skiniotis

    Vydáno 2015
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  19. 19
    Advances in understanding of pathogenesis of aHUS and HELLP

    Advances in understanding of pathogenesis of aHUS and HELLP Autor Celia J. Fang, Anna Richards, M. Kathryn Liszewski, David Kavanagh, John P. Atkinson

    Vydáno 2008
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  20. 20
    Ten candidate ADAMTS13 mutations in six French families with congenital thrombotic thrombocytopenic purpura (Upshaw–Schulman syndrome)

    Ten candidate ADAMTS13 mutations in six French families with congenital thrombotic thrombocytopenic purpura (Upshaw–Schulman syndrome) Autor Agnès Veyradier, J. M. Lavergne, Anne‐Sophie Ribba, Bernadette Obert, Chantal Loirat, D Meyer, J.‐P. Girma

    Vydáno 2004
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