Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Angela Rivers"'
Publikováno v:
Haematologica, Vol 104, Iss 12 (2019)
Externí odkaz:
https://doaj.org/article/48108971c8074c79a223f4c5d34ce3fd
Autor:
Angela Rivers, Kestis Vaitkus, Vinzon Ibanez, Maria Armila Ruiz, Ramasamy Jagadeeswaran, Yogen Saunthararajah, Shuaiying Cui, James D. Engel, Joseph DeSimone, Donald Lavelle
Publikováno v:
Haematologica, Vol 101, Iss 6 (2016)
Increased fetal hemoglobin levels lessen the severity of symptoms and increase the lifespan of patients with sickle cell disease. Hydroxyurea, the only drug currently approved for the treatment of sickle cell disease, is not effective in a large prop
Externí odkaz:
https://doaj.org/article/b268484467364ba99d899853ae8b0cd9
Autor:
Anne Gallivan, Mikail Alejandro, Amarachi Kanu, Nebeyat Zekaryas, Hart Horneman, Lenny K. Hong, Elliott Vinchinsky, Don Lavelle, Alan M. Diamond, Robert E. Molokie, Jagadeesh Ramasamy, Angela Rivers
Publikováno v:
Experimental Hematology. 122:55-62
Autor:
Anne Gallivan, Amarachi Kanu, Mikail Alejandro, Nebeyat Zekaryas, Hart Horneman, Jagadeesh Ramasamy, Lenny Hong, Donald Lavelle, Alan Diamond, Robert E. Molokie, Elliott P. Vichinsky, Angela Rivers
Publikováno v:
Blood. 140:8239-8240
Autor:
Angela Rivers
Publikováno v:
The Journal of Pediatrics. 220:264-267
Autor:
William T Zempsky, Mary Yanaros, Mohammed Sayeem, Donna Boruchov, Connie M Piccone, Deepa Manwani, Crawford Strunk, Immacolata Tartaglione, Raffaella Colombatti, Sophia Akatue, Bianca Oteng, Ahmed Owda, Rose Bamfo, Samuel Wilson, Angela Rivers, Fatimah Farooq, Rebekah Urbonya, Gifty Dankwah Boatemaa, Sudha Rao, Baba Inusa, Charles Antwi-Boasiako, Catherine Segbefia, Fredericka Sey, Biree Andemariam, Eugenia Vicky Asare, Andrew D Campbell
Objectives Sickle Cell Disease (SCD) is a genetic blood disorder affecting over 1 million people globally. The aim of this analysis is to explore the pain burden of patients with SCD in two countries: the United States and Ghana. Methods The Consorti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58350059a74d1ee6f93c6e9f59bc1a24
http://hdl.handle.net/11591/465294
http://hdl.handle.net/11591/465294
Publikováno v:
Haematologica
As high fetal hemoglobin levels ameliorate the underlying pathophysiological defects in sickle cell anemia and beta (β)-thalassemia, understanding the mechanisms that enforce silencing of fetal hemoglobin postnatally offers the promise of effective
Publikováno v:
Health Education Journal. 79:253-265
Objective: A multidisciplinary team from a US midwestern urban medical centre developed written patient education materials for a group education programme designed to prepare adolescents and emerging adults with sickle cell disease for transition to
Autor:
Charles Antwi-Boasiako, Eugenia Vicky Asare, Donna Boruchov, Connie M. Piccone, Fatimah Farooq, Laura Sainati, Silverio Perrotta, Biree Andemariam, William T. Zempsky, Raffaella Colombatti, Immacolata Tartaglione, Rebekah Urbonya, Catherine I. Segbefia, Andrew D. Campbell, Deepa Manwani, Fredericka Sey, Gifty Dankwah Boatemaa, Sudha Rao, Crawford John Strunk, Baba Inusa, Angela Rivers
Publikováno v:
J Racial Ethn Health Disparities
Millions are affected by Sickle Cell Disease (SCD) worldwide with the greatest burden in sub-Saharan Africa. While its origin lies historically within the malaria belt, ongoing changes in migration patterns have shifted the burden of disease resultin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d124b5bf5dd138c01b556aad10638b01
http://hdl.handle.net/11591/430151
http://hdl.handle.net/11591/430151
Autor:
Ashya Smith, Samuel Wilson, William T. Zempsky, Donna Boruchov, Gifty Dankwah Boatemaa, Silverio Perrotta, Catherine I. Segbefia, Sudha Rao, Laura Sainati, Angela Rivers, Ivy Ekem, Connie M. Piccone, Fredericka Sey, Andrew D. Campbell, Charles Antwi-Boasiako, Eugenia Vicky Asare, Immacolata Tartaglione, Crawford John Strunk, Esther Kim, Raffaella Colombatti, Rebekah Urbonya, Fatimah Farooq, Baba Inusa, Haikel Haile, Biree Andemariam, Deepa Manwani
Publikováno v:
Blood Cells Mol Dis
Background: Sickle cell disease (SCD) is characterized by frequent, unpredictable pain episodes and other vaso-occlusive crises (VOCs) leading to significant healthcare utilization. VOC frequency is often an endpoint in clinical trials investigating
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::457154d98a0b6fca1a8d22bdf15686d9
http://hdl.handle.net/11591/458237
http://hdl.handle.net/11591/458237