Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Catherine Nabaggala"'
Autor:
Vincent Mboizi, Catherine Nabaggala, Deogratias Munube, John M. Ssenkusu, Phillip Kasirye, Samson Kamya, Michael G. Kawooya, Amelia Boehme, Frank Minja, Ezekiel Mupere, Robert Opoka, Caterina Rosano, Richard Idro, Nancy S. Green
Publikováno v:
Contemporary Clinical Trials Communications, Vol 42, Iss , Pp 101404- (2024)
Background: Children with sickle cell anemia (SCA) in Sub-Saharan Africa are at high risk of sickle cerebrovascular injury (SCVI). Hydroxyurea, a commonly used disease-modifying therapy, may reduce SCVI resulting in potential impact on reducing strok
Externí odkaz:
https://doaj.org/article/cc3fdc9015f14c47935d802e52026a20
Autor:
Bjarne Robberstad, Bjørn Blomberg, Russell E Ware, Robert O Opoka, David Teigen, Philip Kasirye, Catherine Nabaggala, Heather A Hume, Chandy C John
Publikováno v:
BMJ Global Health, Vol 7, Iss Suppl 2 (2022)
Externí odkaz:
https://doaj.org/article/13b1494196504a9ea7c6d4a8d1017748
Autor:
Ronald Olum, Catherine Nabaggala, Victoria Katasi Mwebe, Ruth Namazzi, Deogratias Munube, Sabrina Bakeera Kitaka
Publikováno v:
Clinical Case Reports, Vol 9, Iss 9, Pp n/a-n/a (2021)
Abstract Orbital compression syndrome is a rare acute complication of sickle cell disease that may impair vision. Assessment by a multidisciplinary team incorporates detailed history and physical examination, fundoscopy, and appropriate imaging to ex
Externí odkaz:
https://doaj.org/article/40c1c958e6d5482eb35512a548c3f9f3
Autor:
David Teigen, Robert O Opoka, Philip Kasirye, Catherine Nabaggala, Heather A Hume, Bjørn Blomberg, Chandy C John, Russell E Ware, Bjarne Robberstad
Publikováno v:
Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40926cd0e4228f3628d96e110641e285
https://doi.org/10.1136/bmjgh-2022-isph.27
https://doi.org/10.1136/bmjgh-2022-isph.27
Autor:
Adam Lane, Teresa Latham, Chandy C. John, Robert O. Opoka, Christopher M. Ndugwa, Heather Hume, Catherine Nabaggala, Phillip Kasirye, Russell E. Ware
Publikováno v:
New England Journal of Medicine. 382:2524-2533
Hydroxyurea has proven safety, feasibility, and efficacy in children with sickle cell anemia in sub-Saharan Africa, with studies showing a reduced incidence of vaso-occlusive events and reduced mortality. Dosing standards remain undetermined, however
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a5ac6390f03d3b02b576feaf0afe1ce
https://doi.org/10.1056/nejmoa2000146
https://doi.org/10.1056/nejmoa2000146
Autor:
Sabrina Bakeera Kitaka, Victoria Katasi Mwebe, Ronald Olum, Catherine Nabaggala, Ruth Namazzi, Deogratias Munube
Publikováno v:
Clinical Case Reports, Vol 9, Iss 9, Pp n/a-n/a (2021)
Clinical Case Reports
Clinical Case Reports
Orbital compression syndrome is a rare acute complication of sickle cell disease that may impair vision. Assessment by a multidisciplinary team incorporates detailed history and physical examination, fundoscopy, and appropriate imaging to exclude inf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf07c5a59ef9e75b68c6342d1ae5ed7a
https://doi.org/10.1002/ccr3.4766
https://doi.org/10.1002/ccr3.4766