Epidemiology of stroke in sickle cell disease

FJ Kirkham, IA Lagunju - Journal of Clinical Medicine, 2021 - mdpi.com
Sickle cell disease is the most common cause of stroke in childhood, both ischaemic and
haemorrhagic, and it also affects adults with the condition. Without any screening or …

Genetic variation and sickle cell disease severity: a systematic review and meta-analysis

JK Kirkham, JH Estepp, MJ Weiss… - JAMA Network …, 2023 - jamanetwork.com
Importance Sickle cell disease (SCD) is a monogenic disorder, yet clinical outcomes are
influenced by additional genetic factors. Despite decades of research, the genetics of SCD …

Sickle cell trait and the potential risk of severe coronavirus disease 2019—A mini‐review

TA Kehinde, MA Osundiji - European Journal of Haematology, 2020 - Wiley Online Library
Abstract Coronavirus Disease 2019 (COVID‐19) pandemic is a rapidly evolving public
health problem. The severity of COVID‐19 cases reported hitherto has varied greatly from …

The BACH1 inhibitor ASP8731 inhibits inflammation and vaso-occlusion and induces fetal hemoglobin in sickle cell disease

JD Belcher, S Nataraja, F Abdulla, P Zhang… - Frontiers in …, 2023 - frontiersin.org
In sickle cell disease (SCD), heme released during intravascular hemolysis promotes
oxidative stress, inflammation, and vaso-occlusion. Conversely, free heme can also activate …

Heme oxygenase-1 and hemopexin gene polymorphisms and the risk of anti-tuberculosis drug-induced hepatotoxicity in China

W Liu, L Lu, H Pan, X He, M Zhang, N Wang… - …, 2022 - Taylor & Francis
Objective: To assess whether the risk of anti-tuberculosis drug-induced hepatotoxicity
(ATDH) might be influenced by heme oxygenase-1 (HMOX1) and hemopexin (HPX) gene …

Protocol for “Genetic composition of sickle cell disease in the Arab population: A systematic review”

F Ata, Z Yousaf, S Sardar, S Javed, P Iqbal… - Health Science …, 2022 - Wiley Online Library
Abstract Background Sickle Cell Disease (SCD) is a global health issue in hematology with
a progressively increasing prevalence. There are recent advances in the management of …

[HTML][HTML] Polymorphisms in the heme oxygenase-1 and bone morphogenetic protein receptor type 1b genes and estimated glomerular filtration rate in Brazilian sickle …

O Chinedu, WV Tonassé, DM Albuquerque… - … , Transfusion and Cell …, 2021 - SciELO Brasil
Introduction Mutations affecting genes involved in oxidative and signaling pathways may be
associated with kidney disease in sickle cell anemia. We determined the allele and …

Transforming growth factor-β1: relation between its single-nucleotide genetic variants and sickle cell nephropathy

M Hamdy, I Shaheen, H Ramadan… - Egyptian Pediatric …, 2024 - Springer
Background Sickle cell nephropathy is a complication of sickle cell disease characterized by
functional abnormalities of the kidney and glomeruli. Our study aimed to investigate the …

CCR5-Δ32 gene variant frequency in the Turkish Cypriot population

U Fahrioglu, MC Ergoren, G Mocan - Brazilian Journal of Microbiology, 2020 - Springer
Recent UNAIDS reports (December 2019) indicate that 37.9 million people have been
affected by HIV infection around the globe in 2018, of which 1.7 million are cited as new …

Significance of heme oxygenase-1(HMOX1) gene on fetal hemoglobin induction in sickle cell anemia patients

P Hariharan, V Chavan, A Nadkarni - Scientific Reports, 2020 - nature.com
Though the patients with sickle cell anemia (SCA) inherit same genetic mutation, they show
considerable phenotypic heterogeneity. It has been observed that patients with elevated …