Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Halima Al Balushi"'
Publikováno v:
Frontiers in Physiology, Vol 10 (2019)
Oxidative damage to red blood cells (RBCs) may contribute to pathogenesis of sickle cell anemia. Reducing the deleterious effects of oxidants by exposing RBCs to a number of antioxidants has been shown to have protective effects against lipid and pro
Externí odkaz:
https://doaj.org/article/4dbec1d684f04d5b9bcb2eb209b2b8e0
Autor:
Halima Al Balushi, Kobina Dufu, David C. Rees, John N. Brewin, Anke Hannemann, Donna Oksenberg, David C.‐Y. Lu, John S. Gibson
Publikováno v:
Physiological Reports, Vol 7, Iss 6, Pp n/a-n/a (2019)
Abstract Sickle cell anemia (SCA) is one of the commonest severe inherited disorders. Nevertheless, effective treatments remain inadequate and novel ones are avidly sought. A promising advance has been the design of novel compounds which react with h
Externí odkaz:
https://doaj.org/article/9c3d3183d1f64aec9f3a922b887157e1
Autor:
John Brewin, Sanjay Tewari, Anke Hannemann, Halima Al Balushi, Claire Sharpe, John S. Gibson, David C. Rees
Publikováno v:
HemaSphere, Vol 1, Iss 1 (2017)
Abstract. The early stages of sickle cell nephropathy (SCN) manifest in children with sickle cell anemia (SCA) as hyperfiltration and proteinuria. The physiological conditions of the renovascular system are among the most conducive to hemoglobin S po
Externí odkaz:
https://doaj.org/article/80c56d0d1dd34c8780da8601f9514181
Autor:
John N. Brewin, Maha Al Awadi, Taimoora Al‐Subhi, Anke Hannemann, Halima Al Balushi, John S. Gibson, Yasser Wali, David C. Rees
Publikováno v:
British Journal of Haematology. 179:256-265
Studying different sickle cell genotypes may throw light on the pathogenesis of sickle cell disease (SCD). Here, the clinical profile, red cell sickling and K+ permeability in 29 SCD patients (15 patients with severe disease and 14 with a milder form
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a9826fb5147a28e44536808f1142a4ec
https://doi.org/10.1111/bjh.14851
https://doi.org/10.1111/bjh.14851
Publikováno v:
Frontiers in Physiology
Frontiers in Physiology, Vol 10 (2019)
Frontiers in Physiology, Vol 10 (2019)
Oxidative damage to red blood cells (RBCs) may contribute to pathogenesis of sickle cell anaemia. Reducing the deleterious effects of oxidants by exposing RBCs to a number of antioxidants has been shown to have protective effects against lipid and pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d4b87b604047435b061fab1e2447acd
https://www.repository.cam.ac.uk/handle/1810/294998
https://www.repository.cam.ac.uk/handle/1810/294998
Publikováno v:
Physiological Reports
Red cells from patients with sickle cell anemia (SCA) are under greater oxidative challenge than those from normal individuals. We postulated that oxidants generated by xanthine oxidase (XO) and hypoxanthine (HO) contribute to the pathogenesis of SCA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e1b072f9b0459f2757f37539ee8500e
Autor:
John N. Brewin, Kobina Dufu, David C. Rees, David C.-Y. Lu, Anke Hannemann, Halima Al Balushi, Donna Oksenberg, John S. Gibson
Publikováno v:
Physiological Reports, Vol 7, Iss 6, Pp n/a-n/a (2019)
Physiological Reports
Physiological Reports
Sickle cell anemia (SCA) is one of the commonest severe inherited disorders. Nevertheless, effective treatments remain inadequate and novel ones are avidly sought. A promising advance has been the design of novel compounds which react with hemoglobin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c61cca9a08ae56919ea574805bcffc8
https://doi.org/10.14814/phy2.14027
https://doi.org/10.14814/phy2.14027
Autor:
Sabah Al Mahrooqi, Arwa Z. Al Riyami, Mohammed Al Huneini, Tamima Al Dughaishi, Moza Al Salmani, Halima Al Balushi, Salam Alkindi, Nihal Al Riyami, Murtadha Al-Khabori, Saif Al Hosni, Sumaiya Al Hinai, Khalil Al-Farsi, Vaidyanathan Gowri, Sabria Al Hashami
Publikováno v:
Transfusion. 54:238-243
Background The management of pregnant women with anti-Jsb is challenging due to the paucity of antigen-negative blood for fetal and neonatal transfusion. Case Report A 29-year-old woman with anti-Jsb was referred for assessment of recurrent fetal los
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fba6e34215b298e2955261be19077bdd
https://doi.org/10.1111/trf.12331
https://doi.org/10.1111/trf.12331
Autor:
Sanjay Tewari, Halima Al Balushi, Oluwabukola T. Gbotosho, David C. Rees, Anke Hannemann, John S. Gibson
Publikováno v:
Tewari, S, Rees, D C, Hannemann, A, Gbotosho, O T, Al Balushi, H W M & Gibson, J S 2016, ' Nocturnal enuresis and K+ transport in red blood cells from patients with sickle cell anemia ', Haematologica, vol. 101, no. 12, pp. e469-e472 . https://doi.org/10.3324/haematol.2016.149500
Sickle cell anemia (SCA) is one of the commonest severe inherited disorders affecting millions worldwide. Complications are extensive although severity varies markedly. Renal damage [or sickle cell nephropathy (SCN)] occurs in approximately one-third
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85f44d15a611cdc58ddb2eb4f384fa1d
Autor:
Stephan Menzel, Sanjay Tewari, Halima Al Balushi, Anke Hannemann, John S. Gibson, Swee Lay Thein, Bukola T Gbotosho, David C. Rees
Publikováno v:
Blood. 128:1317-1317
Background: Patients with sickle cell disease (SCD) have the abnormal haemoglobin (Hb) HbS in their red blood cells (RBCs). The complications of SCD may be extensive but are markedly variable between patients. Renal damage (sometimes called sickle ce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e06420307c94925f864e9afdec90ad6a
https://doi.org/10.1182/blood.v128.22.1317.1317
https://doi.org/10.1182/blood.v128.22.1317.1317