Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Funmilayo Orebayo"'
Autor:
Dimitris A. Tsitsikas, Rhys Hall, John Meenan, Funmilayo Orebayo, Oloruntoyin Bello‐Sanyaolu, Saket Badle, Manisha Sharma, Susan Jain, Jun Liong Chin
Publikováno v:
eJHaem, Vol 2, Iss 1, Pp 118-120 (2021)
Externí odkaz:
https://doaj.org/article/15dbfd5c969d4d1c8aa24e2e4a43babf
Autor:
Diana Mihalca, Adeel Ahmad, Dipal Mehta, Tanya Freeman, Funmilayo Orebayo, Oloruntoyin Bello‐Sanyaolu, Natasha Lewis, Basabi Chatterjee, Dimitris A. Tsitsikas
Publikováno v:
Transfusion Medicine.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4890b45a7dfc5fa3786aa70a3db7f158
https://doi.org/10.1111/tme.12963
https://doi.org/10.1111/tme.12963
Autor:
Dimitris A. Tsitsikas, Basabi Chatterjee, Oloruntoyin Bello-Sanyaolu, Stephanie Coughlin, Rhys Hall, John Meenan, Alvin Katumba, Natasha Lewis, Diana Mihalca, Saket Badle, Dede-Kossi Osakonor, Funmilayo Orebayo
Publikováno v:
British Journal of Haematology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f70af70c1d606ceb14ede366794a554e
https://doi.org/10.1111/bjh.17740
https://doi.org/10.1111/bjh.17740
Autor:
Jun Liong Chin, Susan Jain, Funmilayo Orebayo, Rhys Hall, Oloruntoyin Bello-Sanyaolu, John Meenan, Dimitris A. Tsitsikas, Manisha Sharma, Saket Badle
Publikováno v:
eJHaem. 2:118-120
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a1ef6a3d7b8ed2f25f70152f4431279
https://doi.org/10.1002/jha2.150
https://doi.org/10.1002/jha2.150
Autor:
Dimitris A. Tsitsikas, Diana Mihalca, Stephen Hibbs, Tanya Freeman, Oloruntoyin Bello-Sanyaolu, Funmilayo Orebayo, Natasha Lewis, Laura Green
Publikováno v:
Transfusion and Apheresis Science. 61:103375
Sickle cell disease results in systemic inflammation even at steady state and this is accentuated during acute crises. The plasma of affected patients contains several proinflammatory cytokines as well as adhesion molecules and prothrombotic factors.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87cc17d81e10f750a8c8211dcce67c02
https://doi.org/10.1016/j.transci.2022.103375
https://doi.org/10.1016/j.transci.2022.103375
Autor:
Dimitris A. Tsitsikas, Jibril Abukar, Funmilayo Orebayo, Saket Badle, Manisha Sharma, Afsana Mulla, Natasha Lewis, Roger J. Amos, Rhys Hall, Mohamed Elmi, Oloruntoyin Bello-Sanyaolu, Basabi Chatterjee, Shalini Dave, John Meenan
Publikováno v:
Journal of Clinical Medicine, Vol 10, Iss 767, p 767 (2021)
Journal of Clinical Medicine
Volume 10
Issue 4
Journal of Clinical Medicine
Volume 10
Issue 4
Red cell transfusion represents one of the cornerstones of the chronic management of sickle cell disease, as well as its acute complications. Automated red cell exchange can rapidly lower the number of circulating sickle erythrocytes, without causing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2e6374225085e0b84de1757e157fa0c
https://www.mdpi.com/2077-0383/10/4/767
https://www.mdpi.com/2077-0383/10/4/767
Autor:
Rhoda Amposah, Susan Rowe, Diana Mihalca, Susan Olasoji, Oloruntoyin Bello-Sanyaolu, Dimitris A. Tsitsikas, Lawrence Tham, Funmilayo Orebayo
Publikováno v:
Transfusion and Apheresis Science. 60:103226
Fat embolism syndrome in sickle cell disease is associated with great mortality, while more than half of survivors suffer severe neurological sequelae. Release of fat droplets leads to obstruction of the microcirculation as well as generation of proi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17fdbd2c80a7d60c301f7a4cb8a8c739
https://doi.org/10.1016/j.transci.2021.103226
https://doi.org/10.1016/j.transci.2021.103226
Publikováno v:
Transfusion and Apheresis Science. 56:713-716
Two main sub-phenotypes have been described in sickle cell disease: one with higher baseline haemoglobin and a higher rate of painful crises and one with lower baseline haemoglobin, increased markers of haemolysis and a higher incidence of pulmonary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06ef2b2d1f867913d76aeeed78e2b390
https://doi.org/10.1016/j.transci.2017.08.001
https://doi.org/10.1016/j.transci.2017.08.001
Autor:
Dimitris A. Tsitsikas, Alexander Calvey, Janine Collins, Roger J. Amos, Funmilayo Orebayo, Ruben Nzouakou, Bala Sirigireddy, Natasha Lewis, Sophie Todd, Joanne Quinn
Publikováno v:
Journal of Clinical Apheresis. 31:545-550
We report here our experience with regular automated red cell exchange transfusion for the management of chronic complications of sickle cell disease in 50 patients in our institution from June 2011 to December 2014. The mean sickle hemoglobin level
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99abbf481a9e92c3f6b49d4f44b28370
https://doi.org/10.1002/jca.21447
https://doi.org/10.1002/jca.21447
Autor:
Dimitris A, Tsitsikas, Bala, Sirigireddy, Ruben, Nzouakou, Alexander, Calvey, Joanne, Quinn, Janine, Collins, Funmilayo, Orebayo, Natasha, Lewis, Sophie, Todd, Roger J, Amos
Publikováno v:
Journal of clinical apheresis. 31(6)
We report here our experience with regular automated red cell exchange transfusion for the management of chronic complications of sickle cell disease in 50 patients in our institution from June 2011 to December 2014. The mean sickle hemoglobin level
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::abced7dbf5bb8a1cf5555535fce734ed
https://pubmed.ncbi.nlm.nih.gov/26878828
https://pubmed.ncbi.nlm.nih.gov/26878828