Browsing by Author "Guarda, Caroline Conceição da"
Now showing items 1-20 of 31
-
Association of classical markers and establishment of the dyslipidemic sub-phenotype of sickle cell anemia
Aleluia, Milena Magalhães et al. | Date Issued: 2017 -
Association of homocysteine and inflammatory related molecules in sickle cell anemia
Vilas-Boas, Wendell et al. | Date Issued: 2015 -
Association of the clinical profile and overall survival of pediatric patients with acute lymphoblastic leukemia
Correa, Bruno Terra et al. | Date Issued: 2023 -
CAT -21A>T variant alters hydroxyurea pharmacokinetic parameters in Brazilian children with sickle cell anemia
Yahouédéhou, Sètondji Cocou Modeste Alexandre et al. | Date Issued: 2022 -
Células endoteliais ativadas pelo heme: avaliação de diferentes abordagens terapêuticas
Guarda, Caroline Conceição da | Date Issued: 2015A anemia falciforme (AF) é uma doença genética, que possui quadro clínico heterogêneo, caracterizado por crises de dor, priapismo, síndrome torácica aguda, acidente vascular cerebral (AVC) e eventos hemolíticos, dentre ... -
Comparative study of sickle cell anemia and hemoglobin SC disease: clinical characterization, laboratory biomarkers and genetic profiles
Aleluia, Milena Magalhães et al. | Date Issued: 2017 -
A description of the hemolytic component in sickle leg ulcer: the role of circulating miR-199a-5p, miR-144, and miR-126
Santos, Edvan do Carmo et al. | Date Issued: 2022 -
Differential gene expression analysis of sickle cell anemia in steady and crisis state
Zanette, Dalila Lucíola et al. | Date Issued: 2019 -
Doença falciforme: biomarcadores laboratoriais e inflamatórios associados a manifestações clínicas e uso da hidroxiuréia
Guarda, Caroline Conceição da | Date Issued: 2019INTRODUÇÃO: A doença falciforme (DF) é um grupo de hemoglobinopatias onde a anemia falciforme (AF), caracterizada pela homozigose HbSS, é a forma mais grave, enquanto a hemoglobinopatia SC (HbSC), apesar de menos grave, é ... -
Endothelial nitric oxide synthase (-786T>C) and endothelin-1 (5665G>T) gene polymorphisms as vascular dysfunction risk factors in sickle cell anemia
Vilas-Boas, Wendell et al. | Date Issued: 2016 -
Evaluation of Cardiometabolic Parameters among Obese Women Using Oral Contraceptives
Ferreira, Júnia Raquel Dutra et al. | Date Issued: 2017 -
Fator de transformação do crescimento beta e polimorfismos no gene do receptor 3 do fator de transformação do crescimento beta na doença falciforme
Santiago, Rayra Pereira | Date Issued: 2020INTRODUÇÃO: o fator de transformação do crescimento beta (TGF-\03B2) é uma citocina com papel importante em processos biológicos, como disfunção endotelial e vascular, inflamação e homeostase hematopoiética. OBJETIVO: o ... -
Genetic modulation of fetal hemoglobin in hydroxyurea-treated sickle cell anemia
Aleluia, Milena Magalhães et al. | Date Issued: 2017 -
Genetic Polymorphisms Associated with Environmental Exposure to Polycyclic Derivatives in African Children
Oliveira, Rodrigo Mota de et al. | Date Issued: 2018 -
Heme changes HIF-α, eNOS and nitrite production in HUVECs after simvastatin, HU, and ascorbic acid therapies
Guarda, Caroline Conceição da et al. | Date Issued: 2016 -
Heme-mediated cell activation: the inflammatory puzzle of sickle cell anemia
Guarda, Caroline Conceição da et al. | Date Issued: 2017 -
Hemoglobin Variant Profiles among Brazilian Quilombola Communities
Santiago, Rayra Pereira et al. | Date Issued: 2017 -
Hydroxyurea alters circulating monocyte subsets and dampens its inflammatory potential in sickle cell anemia patients
Guarda, Caroline Conceição da et al. | Date Issued: 2019 -
Hydroxyurea alters hematological, biochemical and inflammatory biomarkers in Brazilian children with SCA: Investigating associations with βS haplotype and α-thalassemia
Yahouédéhou, Sètondji Cocou Modeste Alexandre et al. | Date Issued: 2019 -
Hydroxyurea in the management of sickle cell disease: pharmacogenomics and enzymatic metabolism
Yahouédéhou, Sètondji Cocou Modeste Alexandre et al. | Date Issued: 2018