Zobrazeno 91 - 100
of 302
pro vyhledávání: '"Winfred C Wang"'
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
Publikováno v:
Statistics in Medicine. 26:2836-2852
There are many practical situations where observation of the primary variable Y for individuals in a population is incomplete and depends on some auxiliary variables X that are potentially correlated with Y. We consider parameter estimation for the d
Autor:
Kathleen J. Helton, Matthew P. Smeltzer, Jane E. Schreiber, Guolian Kang, Winfred C. Wang, Maria I Cancio
Publikováno v:
British journal of haematology. 171(1)
Summary Silent cerebral infarctions (SCI) are the most common neurological injury in children with sickle cell anaemia (SCA), but their incidence/prognosis in early childhood has not been well described. We report clinical, neuroradiological, psychom
Autor:
Winfred C. Wang
Publikováno v:
Jornal de Pediatria (Versão em Português), Vol 91, Iss 3, Pp 210-212 (2015)
Jornal de Pediatria, Vol 91, Iss 3, Pp 210-212 (2015)
Jornal de Pediatria, Vol 91, Iss 3, Pp 210-212 (2015)
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:
Jane S. Hankins, Russell E. Ware, Banu Aygun, Courtney D. Thornburg, Kerri Nottage, Matthew P. Smeltzer, Winfred C. Wang
Publikováno v:
Medicine, vol 93, iss 28
Medicine
Medicine
Despite documented laboratory and clinical benefits of hydroxyurea for children with sickle cell anemia (SCA), the drug's long-term safety and efficacy remains poorly defined. The HUSOFT trial and extension study examined feasibility, toxicity, and h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf555c549c4be6c693007efd6cb13af8
https://escholarship.org/uc/item/0hm2k2mf
https://escholarship.org/uc/item/0hm2k2mf
Autor:
Winfred C. Wang, Donald Brambilla, Nancy F. Olivieri, Lori Styles, Knashawn H. Morales, Robert J. Adams, Charles D. Scher
Publikováno v:
The Journal of Pediatrics. 147:244-247
Objective To determine whether long-term transfusion improves growth in children with sickle cell anemia. Study design In the Stroke Prevention Trial for Sickle Cell Anemia Study, patients were randomized to receive long-term transfusion (CTX) or sta
Autor:
Winfred C. Wang, Jonathan C. Goldsmith
Publikováno v:
The Lancet. 381:886-888
Publikováno v:
American Journal of Roentgenology. 183:1117-1122
High blood flow velocity in the middle cerebral artery or distal internal carotid artery, as measured by nonduplex transcranial Doppler sonography, predicts stroke in children with sickle cell anemia. However, velocities measured using the more widel
Autor:
Robert J. Adams, Winfred C. Wang, Suzanne Granger, Miguel R. Abboud, Charles H. Pegelow, Jonathan S. Lewin, Joel K. Curé, Donald Brambilla, Lewis L. Hsu, Robert A. Zimmermann, Dianne Gallagher, Gerald M. Woods, Brian Berman
Publikováno v:
Blood. 103:2822-2826
The stroke prevention study in sickle cell disease (STOP) demonstrated a 90% reduction in stroke risk with transfusion among patients with time-averaged mean cerebral blood velocity (TAMV) of 200 cm/s or more as measured by transcranial Doppler (TCD)