Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Sophia A. T. Parente"'
Autor:
Peter M. Voorhees, Angela Dispenzieri, Alexander Fosså, Amy Chadburn, Megan S. Lim, Makoto Ide, Joshua D Brandstadter, David Wu, Frits van Rhee, Amy D Greenway, Gordan Srkalovic, Wilbur B. Bowne, Thomas S. Uldrick, Sheila K Pierson, Raymond S.M. Wong, Stephen Schey, Mary Jo Lechowicz, Shanmuganathan Chandrakasan, Kazuyuki Yoshizaki, Kojo S.J. Elenitoba-Johnson, Ivan Maillard, Sunita D. Nasta, Razelle Kurzrock, David C. Fajgenbaum, Nikhil C. Munshi, Eric Oksenhendler, Matthew Streetly, Sophia A. T. Parente, Corey Casper
Publikováno v:
Blood Adv
Castleman disease (CD) includes a group of rare and heterogeneous disorders with characteristic lymph node histopathological abnormalities. CD can occur in a single lymph node station, which is referred to as unicentric CD (UCD). CD can also involve
Autor:
Manjula Reddy, Sheila K Pierson, Craig Tendler, Alessia Dalla Pria, Alexander Fosså, Philip Beineke, Nancy A. Shadick, Mark Bower, Sushila A. Shenoy, Christopher S. Nabel, Alexander M. Gorzewski, Michael E. Weinblatt, Sophia A. T. Parente, Jason R. Ruth, Mary Guilfoyle, Laura M. Katz, Ana B Oromendia, Daniel J. Arenas, Taku Kambayashi, David M. Lee, Ruth-Anne Langan Pai, David C. Fajgenbaum, Frits van Rhee, Yasufumi Masaki, Jason G. Mezey
Publikováno v:
Blood Adv
Idiopathic multicentric Castleman disease (iMCD) is a poorly understood hematologic disorder involving cytokine-induced polyclonal lymphoproliferation, systemic inflammation, and potentially fatal multiorgan failure. Although the etiology of iMCD is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bca99d86eae5f7a039e24dd4a68fab32
http://hdl.handle.net/10852/92185
http://hdl.handle.net/10852/92185
Autor:
Ana Luisa Pinto, Dale Kobrin, Maria Leticia Ribeiro, Sophia A. T. Parente, Marília Gomes, David C. Fajgenbaum, Maria Augusta Cipriano
Publikováno v:
Acta Oncologica. 58:515-517
Autor:
Sheila K Pierson, Johnson S. Khor, Maya Blanka Srkalovic, Rozena Rasheed, Mark-Avery Tamakloe, Sophia A. T. Parente, David C. Fajgenbaum, Jasira Ziglar, Dale Kobrin, Taku Kambayashi, Katherine Floess, Daniel Martinez, Daniel J. Arenas, Joseph A. Baur, Gerald Wertheim, Ruth-Anne Langan Pai, David T. Teachey
Publikováno v:
Blood. 135(19)
Idiopathic multicentric Castleman disease (iMCD) is a rare and poorly understood hematologic disorder characterized by lymphadenopathy, systemic inflammation, cytopenias, and life-threatening multiorgan dysfunction. Interleukin-6 (IL-6) inhibition ef