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Frequencies of-308G/A (TNFA) and-509C/T (TGFB1) polymorphisms in sickle cell anemia patients from Brazil
(Funpec-editora, 2013-01-01)
Sickle cell anemia is an affection that causes chronic inflammation, with consequences for vaso-occlusion, oxidative stress and cytokine production. Genetic polymorphisms in markers involved in this process can modulate ...
O gene SPHK1 como potencial influenciador na modulação clínica de pacientes com anemia falciforme: uma revisão
(Universidade Federal do Rio Grande do NorteBrasilUFRNFarmáciaDepartamento de Análises Clínicas e Toxicológicas, 2021-08-27)
Sickle cell disease (SCD) comprise a set of hereditary conditions of great importance given the high number of people worldwide who bear the burden of such diseases. Among these, the one that stands out the most is sickle ...
The impact of the oral condition of children with sickle cell disease on family quality of life
(Universidade Federal de Minas GeraisBrasilFAO - DEPARTAMENTO DE ODONTOPEDIATRIA E ORTODONTIAUFMG, 2016)
Síndrome torácico agudo en pacientes con anemia de células falciformes.
(Universidad Peruana Cayetano Heredia. Facultad de Medicina "Alberto Hurtado", 1997)
Increased concentrations of IL-18 and uric acid in sickle cell anemia: Contribution of hemolysis, endothelial activation and the inflammasome
(2011)
Sickle cell anemia (SCA) is a common, severe monogenetic disorder characterized by chronic hemolysis, frequent infections, a chronic inflammatory state and recurrent occlusions of the microcirculation, resulting in painful ...
Increased concentrations of IL-18 and uric acid in sickle cell anemia: Contribution of hemolysis, endothelial activation and the inflammasome
(2011)
Sickle cell anemia (SCA) is a common, severe monogenetic disorder characterized by chronic hemolysis, frequent infections, a chronic inflammatory state and recurrent occlusions of the microcirculation, result-
ing in painful ...