Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Haydar A Abdelrazig"'
Publikováno v:
Journal of Lipids, Vol 2019 (2019)
Background. Sickle cell disease (SCD) is an inherited haemolytic anemia with a variable course and severity. Knowledge of prognostic biomarkers may help in the establishment of therapeutic intervention, management, and follow-up of patients. There ha
Externí odkaz:
https://doaj.org/article/8cd7b7639159425fb97b9cc8686e1897
Autor:
DalyaMM Abdelmaged, Lamis AA KAddam, Haydar A Abdelrazig, Imad Fadl-Elmula, Abubaker A MohamedSharif, Hassan Elhag Hassan Abdalla, Isra Bdraldein Salih Mohammed, Amal M. Saeed
Background: Sickle cell disease is one of the common genetic diseases with an autosomal recessive inheritance. SCD have been acknowledge as an inflammatory condition with several indicators of an inflammatory response involving high level of white bl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b884b7a487959a383a0c1d2676a2797
https://doi.org/10.21203/rs.3.rs-2109339/v1
https://doi.org/10.21203/rs.3.rs-2109339/v1
Autor:
Imad Fdl-Elmula, and Amal Mahmoud Saeed, Mustafa Khidir Mustafa Elnimeiri, Haydar Awad Abdelrazig, Omer Ali Eisawi, Lamis AbdelGadir Kaddam
Publikováno v:
Blood research
Background Sickle cell anemia (SCA) is a hereditary chronic hemolytic anemia with several clinical consequences. Intravascular sickling of red blood cells leads to multi-organ dysfunction. Moreover, several biochemical abnormalities have been associa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea6a12ce86cad8b45c294d6c741fd12c
http://europepmc.org/articles/PMC6439290
http://europepmc.org/articles/PMC6439290
Autor:
Haydar Awad Abdelrazig, Amal M. Saeed, Omer Ali Eisawi, Lamis AbdelGadir Kaddam, Imad Fadl-Elmula
Publikováno v:
Journal of Lipids
Journal of Lipids, Vol 2019 (2019)
Journal of Lipids, Vol 2019 (2019)
Background. Sickle cell disease (SCD) is an inherited haemolytic anemia with a variable course and severity. Knowledge of prognostic biomarkers may help in the establishment of therapeutic intervention, management, and follow-up of patients. There ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::decb024e64aae70fdaf1fce33fee01a9
http://europepmc.org/articles/PMC6604417
http://europepmc.org/articles/PMC6604417
Autor:
Haydar Awad Abdelrazig, Amal M. Saeed, Florian Lang, Imad Fadl-Elmula, Mohammed Abdelraman Salih, Omer Ali Eisawi, Lamis AbdelGadir Kaddam
Publikováno v:
BMC Hematology
Sickle cell anemia patients suffer from oxidative stress due to chronic inflammation and self-oxidation of sickle hemoglobin (Hb S). Chronic oxidative stress contributes to endothelial dysfunction, inflammation and multiple organ damage in sickle cel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d321f7a246d63736a99a4258e161e34
https://pubmed.ncbi.nlm.nih.gov/28331623
https://pubmed.ncbi.nlm.nih.gov/28331623
Autor:
Omer Ali Eisawi, Lamis AbdelGadir Kaddam, Amal M. Saeed, Imad FdleAlmula, Mustafa Khidir Mustafa Elnimeiri, Haydar Awad Abdelrazig, Florian Lang
Publikováno v:
BMC Hematology
Background High levels of fetal haemoglobin (HbF) decrease sickle cell anaemia (SCA) severity and leads to improved survival. According to in vivo and in vitro studies, butyrate increases HbF production. Its utilization in clinical practice is hamper
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40c460dfd24a05dbd8ebaee93ef2b0d7
https://pubmed.ncbi.nlm.nih.gov/26719803
https://pubmed.ncbi.nlm.nih.gov/26719803
Crimean-Congo hemorrhagic fever (CCHF) is a disease that poses a great threat to public health owing to its high mortality rate (30-70%), mode of transmission and geographic distribution. Here, we report on a nine years-old Sudanese boy from Southern
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4e53a085c536b09a6320ec9a2ec377d3
https://europepmc.org/articles/PMC4949921/
https://europepmc.org/articles/PMC4949921/