Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Winfred C Wang"'
Autor:
Russell E. Ware, Jane S. Hankins, Kerri Nottage, Christina M. Abrams, Guolian Kang, Banu Aygun, Chen Li, Winfred C. Wang, Jeremie H. Estepp, Matthew P. Smeltzer
Publikováno v:
American Journal of Hematology. 92:1333-1339
Hydroxyurea has proven clinical benefits and is recommended to be offered to all children with sickle cell anemia (SCA), but the optimal dosing regimen remains controversial. Induction of red blood cell fetal hemoglobin (HbF) by hydroxyurea appears t
Autor:
Chen Li, Jeffrey D. Lebensburger, Guolian Kang, Jeremie H. Estepp, Jane S. Hankins, Rima S. Zahr, Winfred C. Wang
Publikováno v:
American Journal of Hematology. 94:E27-E29
Autor:
James R. Eckman, Kathryn L. Hassell, Roshni Kulkarni, Naomi L.C. Luban, Cage S. Johnson, Betty S. Pace, Winfred C. Wang, Peter A. Lane, William G. Woods
Publikováno v:
American Journal of Hematology. 84:39-45
The American Society of Pediatric Hematology/Oncology Sickle Cell Summit brought together a broad range of constituencies to identify a unified approach to healthcare and research disparities for sickle cell disease. Recommendations included the foll
Autor:
Winfred C. Wang, Deepika Darbari, Samir K. Ballas, Meredith Milet, Nancy F. Olivieri, Kim Smith-Whitley, Paul Harmatz, Ellen B. Fung, Ward Hagar, William Owen, Elliott Vichinsky, Laura M. De Castro
Publikováno v:
American Journal of Hematology. 82:255-265
A natural history study was conducted in 142 Thalassemic (Thal), 199 transfused Sickle Cell Disease (Tx-SCD, n = 199), and 64 non-Tx-SCD subjects to describe the frequency of iron-related morbidity and mortality. Subjects recruited from 31 centers in
Autor:
Matthew M. Heeney, Martin H. Steinberg, Russell E. Ware, Hong-Yuan Luo, Shawn H. Eung, Winfred C. Wang, David H.K. Chui
Publikováno v:
American Journal of Hematology. 81:361-365
There are approximately 1200 known natural mutations of the human globin genes. In most clinical laboratories, the diagnosis of hemoglobin disorders is based on blood counts, hemoglobin electrophoresis, or column chromatography, which can identify co
Autor:
Patrick Kelly, Carlos Rodriguez-Galindo, Gerald G. Presbury, Michael Jeng, Martha Rieman, Winfred C. Wang
Publikováno v:
American Journal of Hematology. 69:179-184
Langerhans cell histiocytosis (LCH) is a disorder characterized by proliferation of activated Langerhans cells. Immune dysregulation is believed to be part of the pathogenesis. Although current therapies are very effective at inducing remission, mult
Autor:
Vivien A. Sheehan, Jonathan M. Flanagan, Abdullah Kutlar, Winfred C. Wang, Thad A. Howard, Bruce W. Thompson, Russell E. Ware, Zhaoyu Luo
Publikováno v:
American journal of hematology. 88(7)
The recently completed BABY HUG trial investigated the safety and efficacy of hydroxyurea in infants with sickle cell anemia (SCA). To investigate the effects of known genetic modifiers, genomic DNA on 190 randomized subjects were analyzed for alpha
Autor:
Marilyn J. Telen, Kim Smith-Whitley, Samir K. Ballas, Cage S. Johnson, Carolyn Hoppe, Winfred C. Wang, Susan Lieff, Carlton Dampier, Zora R. Rogers, Matthew M. Heeney, Lennette Benjamin
Publikováno v:
American Journal of Hematology.
Sickle cell disease (SCD) is a pleiotropic genetic disorder of hemoglobin that has profound multiorgan effects. The low prevalence of SCD ( approximately 100,000/US) has limited progress in clinical, basic, and translational research. Lack of a large
Autor:
Ed Mitchel, Sadhna M. Shankar, Winfred C. Wang, Marie R. Griffin, Patrick G. Arbogast, William O. Cooper
Publikováno v:
American journal of hematology. 80(4)
The purpose of this study was to evaluate the pattern of medical care utilization and mortality in children and adults with sickle cell disease (SCD) in the state of Tennessee. Rates of hospitalization, emergency department visits, and deaths were me
Publikováno v:
American journal of hematology. 78(1)
Children with sickle cell disease commonly require red blood cell (RBC) transfusion. We report the first case of hemoglobin (Hb) SC disease with development of severe anemia induced by cold agglutinin hemolysis after Mycoplasma infection. Complete bl