Zobrazeno 1 - 10
of 97
pro vyhledávání: '"Winfred C Wang"'
Autor:
Ayobami Olanrewaju, Zachary Abramson, Jane S Hankins, Clifford Takemoto, M. Beth McCarville, Andrew M Heitzer, Guolian Kang, Victoria Okhomina, Winfred C. Wang
Publikováno v:
Blood. 140:2142-2144
Autor:
Akiko Shimamura, Alexey Maschan, Carolyn Bennett, Jason E Farrar, Sujith Samarasinghe, Brigitte Strahm, Winfred C. Wang, Adrianna Vlachos, Charlotte M. Niemeyer, Timothy S. Olson, Denise D'Alessio, Elise Burmeister Getz, Tomasz Lawniczek, Yunnan Xu, David A. Williams
Publikováno v:
Blood. 140:705-707
Autor:
Meghna Dua, Winfred C. Wang, Timothy McCavit, Suvankar Majumdar, R. Clark Brown, Zora R. Rogers, Jeffrey Gossett, Guolian Kang, Jeremie H. Estepp
Publikováno v:
Blood. 140:11108-11109
Autor:
Meghna Dua, Winfred C. Wang, R. Clark Brown, Melissa A. McNaull, Zora R. Rogers, Martha Barton, Jane Hankins, Jeffrey Gossett, Julie Richardson, Jerlym S. Porter, Guolian Kang, Jeremie H. Estepp
Publikováno v:
Blood. 140:445-446
Autor:
Sara R. Rashkin, Evadnie Rampersaud, Jane S. Hankins, Andrew M. Heitzer, Darcy Raches, Jeremie H. Estepp, Winfred C. Wang, Brian Potter, Jennifer Longoria, Allison A. King, Victoria I Okhomina, Guolian Kang
Publikováno v:
Blood. 136:23-24
Background: Fetal hemoglobin (HbF) is the most influential modifier of the clinical and hematologic phenotype of sickle cell disease (SCD) and is highly heritable. Low HbF is independently associated with increased white matter changes on brain imagi
Autor:
Jeremie H. Estepp, Jason R. Hodges, Robert F. Davis, Juan Ding, Nariman Ammar, Guolian Kang, Winfred C. Wang, Jerlym S. Porter, Jane S. Hankins, James G. Gurney, Arash Shaban-Nejad, Hamda Khan
Publikováno v:
Blood. 136:19-19
Introduction Individuals with sickle cell disease (SCD) experience recurrent acute vaso-occlusive events (VOE) beginning in infancy, that can be prevented with hydroxyurea therapy (Wang W. Lancet 2011), while chronic organ dysfunction becomes evident
Autor:
Jason R. Hodges, Lisa M. Jacola, Guolian Kang, Winfred C. Wang, Allison A. King, Jane S. Hankins, Xiwen Zhao, Jerlym S. Porter, Marita Partanen, Pradeep S. B. Podila, Anjelica C. Saulsberry
Publikováno v:
Blood. 134:519-519
Introduction: In the United States, most children with sickle cell disease (SCD) survive into adulthood and transfer from pediatric to adult-centered care. Cognitive deficits begin during childhood and are highly prevalent among individuals with SCD,
Autor:
Winfred C. Wang, Juan Ding, Irene Agodoa, Guolian Kang, Jeremie H. Estepp, Ze Cong, M. Beth McCarville, Jane S. Hankins
Publikováno v:
Blood. 134:1002-1002
Introduction Sickle Cell Anemia (SCA) is a rare, devastating, and debilitating disease marked by the pathophysiologic features of hemolytic anemia, vaso-occlusion, and progressive end-organ damage. The most devastating complication of pediatric SCA i
Autor:
Grace Champlin, Jane S. Hankins, Winfred C. Wang, Kenneth I. Ataga, Curtis L. Owens, Robert F. Davis, Jeremie H. Estepp, Lisa M. Jacola, Juan Ding, Scott N. Hwang, Guolian Kang, Justin Newman, Allison A. King
Publikováno v:
Blood. 134:2290-2290
Introduction Silent cerebral infarcts (SCI) and cerebral vessel stenosis are common and progressive in sickle cell anemia (SCA). Most data regarding brain lesions in SCA are cross-sectional or derive from pediatric cohorts with short follow-up not sp
Autor:
Marcin W. Wlodarski, Janet L. Kwiatkowski, Nolan Neu, Bertil Glader, Mukta Sharma, Heather A. Bradeen, Nina Kollmar, Kevin H.M. Kuo, Melissa J. Rose, D. Holmes Morton, Eduard J. van Beers, Christine M. Knoll, Rachael F. Grace, Heng Wang, Joachim B. Kunz, Jenny M. Despotovic, Wendy B. London, Ellis J. Neufeld, Wilma Barcellini, Alexis A. Thompson, Elisa Fermo, Winfred C. Wang, Hasan Al-Sayegh, Susanne Holzhauer, Melissa M. McNaull, Dongjing Guo, Paola Bianchi, Hassan M. Yaish, Dagmar Pospisilova, Satheesh Chonat, Sujit Sheth, Patrick G. Gallagher, Yaddanapudi Ravindranath, Alberto Zanella, Stefan W. Eber, Vicky R. Breakey, Kimberly Lezon-Geyda, Yves D. Pastore, Jennifer A. Rothman, Peter E. Newburger
Publikováno v:
Blood, 131(20), 2183. American Society of Hematology
An international, multicenter registry was established to collect retrospective and prospective clinical data on patients with pyruvate kinase (PK) deficiency, the most common glycolytic defect causing congenital nonspherocytic hemolytic anemia. Medi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0717f6eb0af1ef676f6102969526c464
https://dspace.library.uu.nl/handle/1874/376400
https://dspace.library.uu.nl/handle/1874/376400