Zobrazeno 1 - 10
of 59
pro vyhledávání: '"Winfred C Wang"'
Autor:
Erica Hodgman, Lynn W. Wynn, Abdelhafeez Abdelhafeez, Andrew J. Murphy, Winfred C. Wang, Sidrah Khan, Amy C. Kimble, Andrew M. Davidoff, Lindsay J. Talbot, Yousef El-Gohary
Publikováno v:
Journal of Pediatric Surgery. 55:2471-2474
Background Partial splenectomy (PS) may allow preservation of splenic function in cases where splenectomy is indicated for hematologic diseases; however, the long-term outcomes are uncertain. We investigated the long-term outcomes of PS in patients w
Autor:
Andrew M. Davidoff, Yousef El-Gohary, Andrew Fleming, Andrew J. Murphy, Hui Zhang, Winfred C. Wang, Jane S. Hankins, Jeremie H. Estepp
Publikováno v:
Journal of Surgical Research. 242:336-341
Individuals with sickle cell disease (SCD) are at high risk of developing life-threatening complications, particularly acute chest syndrome (ACS) postoperatively. The perioperative factors associated with the development of ACS in children with SCD a
Autor:
Andrew M. Davidoff, Winfred C. Wang, Lisa VanHouwelingen, Shenghua Mao, Amos Hong Pheng Loh, John A. Sandoval, Aaron D Seims, Jianrong Wu, Israel Fernandez-Pineda, Jessica Mead
Publikováno v:
Journal of Laparoendoscopic & Advanced Surgical Techniques. 27:206-210
Laparoscopy offers many benefits to splenectomy, such as reduced incisional pain and shortened hospital duration. The purpose of this study is to evaluate procedural and outcome differences between multiport (MP) and reduced port (RP) splenectomy whe
Autor:
Erica I. Hodgman, Yousef El-Gohary, Lindsay J. Talbot, Sidrah Khan, Amy C. Kimble, Abdelhafeez Abdelhafeez, Andrew M. Davidoff, Lynn W. Wynn, Andrew J. Murphy, Winfred C. Wang
Publikováno v:
Journal of the American College of Surgeons. 229:e173
Autor:
Jane S. Hankins, Kathleen J. Helton, Ruitian Song, Adam M. Winchell, Claudia M. Hillenbrand, Winfred C. Wang, Ralf B. Loeffler
Publikováno v:
Journal of Healthcare Engineering
Journal of Healthcare Engineering, Vol 2017 (2017)
Journal of Healthcare Engineering, Vol 2017 (2017)
Purpose. To evaluate a new postprocessing framework that eliminates arterial vessel signal contributions in the quantification of normalized visible venous volume (NVVV, a ratio between venous and brain volume) in susceptibility-weighted imaging (SWI
Autor:
Jane S. Hankins, Banu Aygun, Barry L. Shulkin, Kerri Nottage, Matthew P. Smeltzer, Russell E. Ware, Bryan Winter, Winfred C. Wang, Stephen D. Dertinger
Publikováno v:
European Journal of Haematology. 93:377-383
Background More than 90% of children with sickle cell anemia (SCA) lose splenic function by the age of 2 yrs. Splenic function may improve with hydroxyurea, but previous studies are conflicting. We prospectively evaluated the effect of hydroxyurea on
Autor:
Winfred C. Wang, Abdullah Kutlar, Bruce Thompson, Lori Luchtman-Jones, Thomas H. Howard, Ming Lu, Ram Kalpatthi, Scott T. Miller, Niren Patel
Publikováno v:
Clinical Biochemistry. 46:278-281
To investigate the concordance of blood count indices measured locally and at a central laboratory.In a multi-center clinical trial of hydroxyurea therapy in infants with sickle cell anemia (BABY HUG), the concordance between blood count indices meas
Autor:
Kathleen J. Helton, Kerri Nottage, Banu Aygun, Russell E. Ware, Joseph Moen, Guolian Kang, Matthew P. Smeltzer, Winfred C. Wang, Jane S. Hankins
Publikováno v:
British journal of haematology. 175(2)
Summary Silent cerebral infarction (SCI) is the most common neurological abnormality among children with sickle cell anaemia (SCA). The effect of hydroxycarbamide (also termed hydroxyurea) on the development and progression of SCI is unclear. We eval
Autor:
Winfred C. Wang, Deepika S. Darbari, Samir K. Ballas, Carolyn Hoppe, Ward Hagar, Ifeyinwa Osunkwo, Muge R. Kesen, Gerard A. Lutty, Morton F. Goldberg, Carlton Dampier, Punam Malik
Publikováno v:
The Scientific World Journal, Vol 2012 (2012)
The Scientific World Journal
The Scientific World Journal
The sickle hemoglobin is an abnormal hemoglobin due to point mutation (GAG → GTG) in exon 1 of theβglobin gene resulting in the substitution of glutamic acid by valine at position 6 of theβglobin polypeptide chain. Although the molecular lesion i
Autor:
Ashok Raj, Lewis L. Hsu, Kim Smith-Whitley, Suba Krishnan, Frans A. Kuypers, Lori Styles, Yamaja Setty, Charles T. Quinn, Karen Kesler, Marie J. Stuart, George R. Buchanan, Nigel S. Key, Seungshin Rhee, Winfred C. Wang, Theodore Wun, Kenneth I. Ataga
Publikováno v:
British Journal of Haematology. 155:263-267
Tapered oral dexamethasone for acute chest syndrome (ACS) in sickle cell anaemia was studied using a novel ACS assessment tool and investigational biomarkers. Twelve participants were randomized (mean age 17·3 years) before early study termination.