Polymorphisms and gene expression of metalloproteinases and their inhibitors associated with cerebral ischemic stroke in young patients with sickle cell anemia
Author:
Funder
Capes
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Molecular Biology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s11033-023-08262-2.pdf
Reference48 articles.
1. Miranda CTOF, Vermeulen-Serpa KM, Pedro ACC, Brandão-Neto J, Vale SHL, Figueiredo MS (2022) Zinc in sickle cell disease: a narrative review. J Trace Elem Med Biol 72:126980. https://doi.org/10.1016/j.jtemb.2022.126980
2. Sales RR, Nogueira BL, Tosatti JAG, Gomes KB, Luizon MR (2022) Do genetic polymorphisms affect fetal hemoglobin (HbF) levels in patients with sickle cell anemia treated with hydroxyurea? A systematic review and pathway analysis. Front Pharmacol 12:779497. https://doi.org/10.3389/fphar.2021.779497
3. Vichinksy EP (1997) Understating the morbidity of sickle cell disease. Br J Haematol 99(4):974–976; author reply 976–977. https://doi.org/10.1046/j.1365-2141.1997.5013304.x
4. Higgs DR, Wood WG (2008) Genetic complexity in sickle cell disease. Proc Natl Acad Sci USA 105(33):11595–11596. https://doi.org/10.1073/pnas.0806633105
5. Zago MA, Pinto ACS (2007) The pathophysiology of sickle cell disease: from the genetic mutation to multiorgan dysfunction. Rev Bras Hematol Hemoter 29:207–214. https://doi.org/10.1590/S1516-84842007000300003
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