Zobrazeno 1 - 10
of 308
pro vyhledávání: '"Han-mou Tsai"'
Autor:
Han-Mou Tsai, Elizabeth Kuo
Publikováno v:
Advances in Hematology, Vol 2014 (2014)
Eculizumab is highly effective in controlling complement activation in patients with the atypical hemolytic uremic syndrome (aHUS). However, the course of responses to the treatment is not well understood. We reviewed the responses to eculizumab ther
Externí odkaz:
https://doaj.org/article/1025c7e456f143628564a22867e5f84a
Autor:
Yeong-Hau H. Lien, Han-Mou Tsai
Publikováno v:
The American Journal of Medicine. 135:e423-e424
Autor:
Babak Baseri, Carol Luhrs, Daniel Benasher, Swati M. D. Vishwanathan, Han-Mou Tsai, Mikhail Khazan
Publikováno v:
Journal of Clinical Apheresis. 34:623-630
Acquired thrombotic thrombocytopenic purpura (aTTP) is a serious disorder with arteriolar and capillary thrombosis for which the treatment usually requires plasma exchange with plasma as the replacement fluid. Management of patients who do not accept
Autor:
Han-Mou Tsai
Publikováno v:
The American Journal of Medicine. 132:161-167
Atypical hemolytic uremic syndrome commonly presents with the triad of microangiopathic hemolytic anemia, thrombocytopenia, and renal function impairment without an antecedent hemorrhagic diarrhea. Less known are extrarenal complications due to abnor
Publikováno v:
The American Journal of Case Reports
Patient: Female, 67-year-old Final Diagnosis: Enoxaparin induced thrombocytopenia with life threatening thrombosis Symptoms: Chest discomfort Medication:— Clinical Procedure: — Specialty: Hematology Objective: Educational purpose Background: Hepa
Autor:
Han-Mou Tsai
Publikováno v:
The American journal of medicine. 132(9)
For many years after its first description in 1924, thrombotic thrombocytopenic purpura was an intriguing puzzle for clinicians and researchers, not only for its unique pathology, perplexing changes in von Willebrand factor multimers, and high rate o
Autor:
Han-Mou Tsai
Thrombotic thrombocytopenic purpura, Shiga toxin-associated hemolytic-uremic syndrome and atypical hemolytic-uremic syndrome often present with microangiopathic hemolytic anemia (MAHA) and thrombocytopenia. These disorders are often classified as thr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1034dcfb1ec613cec94deb38e29b99e1
https://doi.org/10.1016/b978-0-12-813456-6.00042-4
https://doi.org/10.1016/b978-0-12-813456-6.00042-4
Autor:
Joseph Alsousou, Dominick J. Angiolillo, Amal Arachiche, Richard H. Aster, Tiziano Barbui, Stefania Basili, Elisabeth M. Battinelli, Anthony A. Bavry, Wolfgang Bergmeier, Gerald Bertrand, Deepak L. Bhatt, Thomas A. Blair, Kamila Bledzka, Oliver Borst, Emma G. Bouck, Lawrence F. Brass, Paul F. Bray, Carol Briggs, Tomasz Brzoska, James B. Bussel, Marco Cattaneo, Subarna Chakravorty, Noel C. Chan, Shruti Chaturvedi, Beng H. Chong, Kenneth J. Clemetson, Jeannine M. Clemetson, Barry S. Coller, Gregory J. del Zoppo, Jenny M. Despotovic, Scott L. Diamond, J. Donald Easton, Koji Eto, Hervé Falet, Francisca Ferrer-Marin, Guido Finazzi, Robert Flaumenhaft, Jane E. Freedman, Andrew L. Frelinger, Kathleen Freson, Aleksandra Gasecka, Meinrad Gawaz, Silvia Giannini, Andreas Greinacher, Thomas Gremmel, Paul A. Gurbel, Elizabeth J. Haining, Xu Han, Paul Harrison, Catherine P.M. Hayward, Karin Hoffmeister, Anne-Mette Hvas, Sara J. Israels, Joseph E. Italiano, Young-Hoon Jeong, Andrew D. Johnson, Cecile Kaplan, Peter Karagiannis, Gregory J. Kato, Samuel Kemble, Kumaran Kolandaivelu, Milka Koupenova, David J. Kuter, Michele P. Lambert, Robert H. Lee, Jack Levin, Renhao Li, Zhenyu Li, Zihai Li, Anqi Li, Rossella Liani, Marie Lordkipanidzé, Viola Lorenz, Kellie R. Machlus, Dhruv Mahtta, Pier Mannuccio Mannucci, Keith R. McCrae, Alessandra Metelli, Alan D. Michelson, Karen A. Moffat, Jae Youn Moon, James H. Morrissey, Nicola J. Mutch, Zoltan Nagy, Heyu Ni, Phillip L.R. Nicolson, Marvin T. Nieman, Rienk Nieuwland, Marie-Blanche Onselaer, Carlo Patrono, Edward F. Plow, Mortimer Poncz, Man-Chiu Poon, Natalie S. Poulter, Izmarie Poventud-Fuentes, Patrick Provost, Jun Qin, Julie Rayes, Alexander P. Reiner, Brian Riesenberg, Irene A.G. Roberts, Matthew T. Rondina, Jesse W. Rowley, Francesca Santilli, Rüdiger E. Scharf, Yotis A. Senis, Anish Sharda, Alexa J. Siddon, Pia R.-M. Siljander, Pierluigi Tricoci, Paola Simeone, Stephanie A. Smith, Susan S. Smyth, Edward L. Snyder, Martha Sola-Visner, Timothy J. Stalker, Lucia Stefanini, Naoshi Sugimoto, Prithu Sundd, Udaya S. Tantry, Ayalew Tefferi, Steven G. Thomas, Mark R. Thomas, Maurizio Tomaiuolo, Christopher A. Tormey, Han-Mou Tsai, Francesco Violi, Theodore E. Warkentin, Steve P. Watson, Jeffrey I. Weitz, John Welsh, Andrew S. Weyrich, David A. Wilcox, Bill X. Wu, Michael R. Yeaman, Li Zhu, Guy A. Zimmerman, Elizabeth R. Zunica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e0944066289be8af9adfd324552f5a4
https://doi.org/10.1016/b978-0-12-813456-6.09991-4
https://doi.org/10.1016/b978-0-12-813456-6.09991-4
Autor:
Han-Mou Tsai, Elizabeth Kuo
Publikováno v:
Obstetrics & Gynecology. 127:907-910
Preeclampsia is a leading cause of morbidity and mortality during pregnancy. The variability of clinical features suggests that preeclampsia is not a single disease. Atypical hemolytic uremic syndrome, resulting from defective regulation of the alter
Publikováno v:
American Journal of Case Reports; 5/29/2020, Vol. 21, p1-7, 7p