Zobrazeno 1 - 10
of 106
pro vyhledávání: '"Isaac Odame"'
Autor:
Samuel T Chatio, Enyonam Duah, Lucy O Ababio, Nicola Lister, Olufolake Egbujo, Kwaku Marfo, Raymond Aborigo, Patrick Ansah, Isaac Odame
Publikováno v:
PLoS ONE, Vol 19, Iss 5, p e0303520 (2024)
IntroductionSickle cell disease (SCD) remains a public health problem especially in sub-Saharan Africa including Ghana. While pilot initiatives in Africa have demonstrated that neonatal screening coupled with early intervention reduces SCD-related mo
Externí odkaz:
https://doaj.org/article/44a6ebacd82f4749853b60efe5e29426
Autor:
Matthew Heeney, David Rees, Mariane de Montalembert, Isaac Odame, Yasser Wali, Sarfaraz Sayyed, Velusamy Shanmuganathan Muthusamy, Anisha E. Mendonza, Michele Nassin, Deborah Keefe, Julie Kanter
Publikováno v:
HemaSphere, Vol 7, p e3247294 (2023)
Externí odkaz:
https://doaj.org/article/493194a7b92d4e5c9be51b353b7c896b
Autor:
Lutz Hegemann, Vas Narasimhan, Kwaku Marfo, Patrick Kuma-Aboagye, Solomon Ofori-Acquah, Isaac Odame
Publikováno v:
Annals of Global Health, Vol 89, Iss 1, Pp 76-76 (2023)
Background: Sickle cell disease (SCD) is a major unresolved global health issue, with the highest disease burden in sub-Saharan African countries; yet, SCD care has not proportionally reached patients in these regions, and the disease has received li
Externí odkaz:
https://doaj.org/article/6c6086d834ce496c8cf242c31d12a5eb
Autor:
Ran An, Yuning Huang, Anne Rocheleau, Alireza Avanaki, Priyaleela Thota, Qiaochu Zhang, Yuncheng Man, Zoe Sekyonda, Catherine I. Segbefia, Yvonne Dei-Adomakoh, Enoch Mensah, Kwaku Ohene-Frempong, Isaac Odame, Amma Owusu-Ansah, Umut A. Gurkan
Publikováno v:
Heliyon, Vol 8, Iss 12, Pp e11778- (2022)
Hemoglobin (Hb) disorders affect nearly 7% of the world’s population. Globally, around 400,000 babies are born annually with sickle cell disease (SCD), primarily in sub-Saharan Africa where morbidity and mortality rates are high. Screening, early d
Externí odkaz:
https://doaj.org/article/3afc83a2f7714440a6ae0b2eeb33d867
Autor:
Ann T. Farrell, Julie Panepinto, Ankit A. Desai, Adetola A. Kassim, Jeffrey Lebensburger, Mark C. Walters, Daniel E. Bauer, Rae M. Blaylark, Donna M. DiMichele, Mark T. Gladwin, Nancy S. Green, Kathryn Hassell, Gregory J. Kato, Elizabeth S. Klings, Donald B. Kohn, Lakshmanan Krishnamurti, Jane Little, Julie Makani, Punam Malik, Patrick T. McGann, Caterina Minniti, Claudia R. Morris, Isaac Odame, Patricia Ann Oneal, Rosanna Setse, Poornima Sharma, Shalini Shenoy
Publikováno v:
Blood Advances, Vol 3, Iss 23, Pp 4002-4020 (2019)
Abstract: To address the global burden of sickle cell disease and the need for novel therapies, the American Society of Hematology partnered with the US Food and Drug Administration to engage the work of 7 panels of clinicians, investigators, and pat
Externí odkaz:
https://doaj.org/article/06caa969e3bd4e5b84bcc4cdd2e86f79
Autor:
Ali Amid, Shiyi Chen, Uma Athale, Karen Charpentier, Manuela Merelles-Pulcini, Isaac Odame, Melanie Kirby-Allen
Publikováno v:
Haematologica, Vol 103, Iss 5 (2018)
Externí odkaz:
https://doaj.org/article/80d73b1d60ab4206ae49ca94c2e63b99
Publikováno v:
Cogent Food & Agriculture, Vol 3, Iss 1 (2017)
Aquaculture is one of the fastest growing industries in the fisheries sector of Ghana, serving as a source of protein, food security, employment creation, economic growth and poverty reduction strategy. The aim of this paper is to assess the awarenes
Externí odkaz:
https://doaj.org/article/cca955a3fc7f4f9297dc6b6b8c045a73
Autor:
Ali Amid, Melina Cheong, Barry Eng, Meredith Hanna, Betty-Ann Hohenadel, Lisa M. Nakamura, Lynda Walker, Isaac Odame, Melanie Kirby-Allen, John S. Waye
Publikováno v:
Haematologica, Vol 100, Iss 5 (2015)
Externí odkaz:
https://doaj.org/article/f7c63fba4fee4952ab816db9b2fdffcc
Autor:
Isaac Odame
Publikováno v:
Archives of Disease in Childhood. 108:108-114
Sickle cell disease (SCD), one of the most common monogenetic diseases in the world, is associated with multisystemic complications that begin in childhood. Most of the babies homozygous for the sickle haemoglobin gene are born in sub-Saharan Africa.
Publikováno v:
British Journal of Haematology. 197:373-376
Owing to the unique pathophysiology of anaemia in haemoglobin Bart's hydrops fetalis (HBHF), a transfusion strategy based on beta-thalassemia guidelines is suboptimal for chronically transfused HBHF patients. A more aggressive transfusion aimed at re