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Psychological development and sickle cell disease: The impact of illness in the exercise of leading activitiesDesenvolvimento do psiquismo e anemia falciforme: O impacto do adoecimento no exercício das atividades principais
(2019-01-01)
Sickle cell disease is a chronic blood disease that leads to numerous and serious implications to the life of its bearers, expressed as physical symptoms, like sickle cell crisis, pulmonary hypertension, acute thoracic ...
Brazilian Guidelines for transcranial doppler in children and adolescents with sickle cell disease
(Associação Brasileira de Hematologia e Hemoterapia e daSociedade Brasileira de Transplante de Medula Óssea, 2011)
BACKGROUND: Sickle cell disease is the most common monogenic hereditary disease in Brazil. Although strokes are one of the main causes of morbidity and mortality in these patients, the use of transcranial Doppler to identify ...
Femoral head necrosis treatment with autologous stem cells in sickle cell disease
(Sociedade Brasileira de Ortopedia e Traumatologia, 2008)
The 844ins68 cystathionine beta-synthase and C677T MTHFR gene polymorphism and the vaso-occlusive event risk in sickle cell disease
(Termedia Publishing House Ltd, 2011-02-01)
Introduction: Sickle cell disease (SCD) is an inflammatory condition with an increase in the adhesion of sickled erythrocytes, and it is a potential cause of vaso-occlusive episodes, an event related to clinical manifestations, ...
Heme-mediated cell activation: the inflammatory puzzle of sickle cell anemia
(Taylor & Francis, 2018)
The Xmnl polymorphic site 5 ' to the gene G gamma in a Brazilian patient with sickle cell anaemia - fetal haemoglobin concentration, haematology and clinical features
(Termedia Publishing House Ltd, 2010-10-01)
We report a 20-year-old female with sickle cell anaemia and with an HbF concentration of 15.8%. The patient was not using hydroxyurea and was not receiving regular blood transfusions. The patient never had chronic ...
The Xmnl polymorphic site 5 ' to the gene G gamma in a Brazilian patient with sickle cell anaemia - fetal haemoglobin concentration, haematology and clinical features
(Termedia Publishing House Ltd, 2010-10-01)
We report a 20-year-old female with sickle cell anaemia and with an HbF concentration of 15.8%. The patient was not using hydroxyurea and was not receiving regular blood transfusions. The patient never had chronic ...
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 ...
Klotho: its various functions and association with sickle cell disease subphenotypes.
(Sociedade Brasileira de Hematologia e Hemoterapia, 2015)