Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Srila, Gopal"'
Publikováno v:
JMIR Public Health and Surveillance, Vol 10, p e57290 (2024)
BackgroundChronic kidney disease (CKD) is a significant complication in patients with sickle cell disease (SCD), leading to increased mortality. ObjectiveThis study aims to investigate the burden of CKD in Medicaid-enrolled adults with SCD in Califo
Externí odkaz:
https://doaj.org/article/e9ba885ac624406993e4d53cfc5b119b
Publikováno v:
Biomedicine & Pharmacotherapy, Vol 156, Iss , Pp 113911- (2022)
β-thalassemia is a genetic hemoglobin (Hb) disorder that affects millions of people world-wide. It is characterized by ineffective erythropoiesis and anemia. The resultant chronic anemia can require life-long blood transfusion regimens, leading to s
Externí odkaz:
https://doaj.org/article/de54c08cc9264bf6be40b1ef68b4eed6
Autor:
Srila Gopal, Qing Lu, Joshua J. Man, Wendy Baur, Sitara P. Rao, Lev Litichevskiy, Malvina Papanastasiou, Amanda L. Creech, Katherine C. DeRuff, James Mullahoo, Adam Officer, Shawn B. Egri, Desiree Davison, Jacob D. Jaffe, Iris Z. Jaffe
Publikováno v:
Blood Advances, Vol 2, Iss 14, Pp 1680-1684 (2018)
Externí odkaz:
https://doaj.org/article/7b02b506272e4750b213161fae36c778
Comprehensive guide to managing a chronic automated red cell exchange program in sickle cell disease
Autor:
Robyn, Cunard, Srila, Gopal, Patricia M, Kopko, Minh-Uyen, Dang, Kathryn M, Hazle, Amber P, Sanchez
Publikováno v:
Journal of Clinical Apheresis. 37:497-506
Sickle cell disease (SCD) is associated with significant morbidity and mortality, and limits both the quality and quantity of life. Transfusion therapy, specifically automated red cell exchange (aRCE), plays a key role in management of SCD and is ben
Autor:
Carlos J Munoz, Cynthia R Muller, Daniela Lucas, Ivan Susin Pires, Andre F Palmer, Srila Gopal, Pedro Cabrales
Publikováno v:
Blood. 140:5405-5406
Publikováno v:
The FASEB Journal. 36
Publikováno v:
Haemophilia : the official journal of the World Federation of HemophiliaREFERENCES. 28(5)
Haemophilia patients experience painful joint episodes which may or may not be associated with haemarthrosis. We sought to validate a questionnaire developed by the Canadian Haemophilia Society using point-of-care musculoskeletal ultrasound (POC MSKU
Publikováno v:
Blood. 140:13045-13045
Autor:
Srila Gopal, Morten A. Karsdal, Tine Wyseure, Chanond A Nasamran, Esther J Cooke, Kathleen M. Fisch, Tina Manon-Jensen, Jenny Y Zhou, Annette von Drygalski, Laurent O. Mosnier
Publikováno v:
J Thromb Haemost
Background Vascular remodeling associated with hemophilic arthropathy (HA) may contribute to bleed propagation, but the mechanisms remain poorly understood. Objectives To explore molecular mechanisms of HA and the effects of hemostasis correction on
Autor:
Srila Gopal, Haowei Linda Sun, Shannon Jackson, Annette von Drygalski, Doris Quon, Richard F. W. Barnes
Publikováno v:
The Journal of Haemophilia Practice. 6:42-50
Background Patients with haemophilia have a higher prevalence of hypertension than the general population that cannot be explained by traditional cardiovascular risk factors such as age, race, diabetes or obesity. Patients with severe haemophilia, wh