Search Results - "Belisario, André Rolim"
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Functional polymorphisms of BCL11A and HBS1L-MYB genes affect both fetal hemoglobin level and clinical outcomes in a cohort of children with sickle cell anemia
Published in Annals of hematology (01-07-2020)“…Fetal hemoglobin (HbF) ameliorates clinical severity of sickle cell anemia (SCA). The major loci regulating HbF levels are HBB cluster, BCL11A , and HMIP-2 (…”
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2
Pharmacogenomic markers of glucocorticoid response in congenital adrenal hyperplasia
Published in PloS one (20-12-2022)“…Glucocorticoids (GC) replacement are the mainstay treatment for 21-hydroxylase deficiency (21-OHD), the most common cause of congenital adrenal hyperplasia…”
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3
Fetal hemoglobin-boosting haplotypes of BCL11A gene and HBS1L-MYB intergenic region in the prediction of clinical and hematological outcomes in a cohort of children with sickle cell anemia
Published in Journal of human genetics (01-12-2022)“…Single nucleotide polymorphisms (SNPs) of BCL11A gene and HBS1L-MYB intergenic region (named HMIP-2) affect both fetal hemoglobin (HbF) concentration and…”
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4
Clinical and Genetic Predictors of Priapism in Sickle Cell Disease: Results from the Recipient Epidemiology and Donor Evaluation Study III Brazil Cohort Study
Published in Journal of sexual medicine (01-12-2019)“…Priapism is the persistent and painful erection of the penis and is a common sickle cell disease (SCD) complication. The goal of this study was to characterize…”
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5
Critical failure of a cell therapy products storage tank: Description, investigation and implemented improvements
Published in Transfusion (Philadelphia, Pa.) (01-01-2023)Get full text
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Prevalence and risk factors for albuminuria and glomerular hyperfiltration in a large cohort of children with sickle cell anemia
Published in American journal of hematology (01-05-2020)Get full text
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Influence of laboratory procedures on postthawing cell viability and hematopoietic engraftment after autologous peripheral blood stem cell transplantation
Published in Transfusion (Philadelphia, Pa.) (01-04-2021)“…Background The kinetics of hematopoietic recovery after autologous stem cell transplantation (ASCT) may be affected by laboratory procedures. The aim of this…”
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Blood utilization and characteristics of patients treated with chronic transfusion therapy in a large cohort of Brazilian patients with sickle cell disease
Published in Transfusion (Philadelphia, Pa.) (01-08-2020)“…BACKGROUND Red blood cell (RBC) transfusions are used in sickle cell disease (SCD) to treat acute complications or as chronic transfusion therapy (CTT) to…”
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9
Association of ZBTB38 gene polymorphism (rs724016) with height and fetal hemoglobin in individuals with sickle cell anemia
Published in Molecular genetics and metabolism reports (01-06-2024)“…Our study evaluated the association of the polymorphism rs724016 in the ZBTB38 gene, previously associated with height in other populations, with predictors of…”
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10
Clinical, laboratory, and molecular characteristics of a cohort of children with hemoglobinopathy S/beta-thalassemia
Published in Hematology, Transfusion and Cell Therapy (01-04-2024)“…Hemoglobinopathy Sβ-thalassemia (HbSβ-thal) has a wide range of clinical and laboratory severity. There is limited information on the natural history of…”
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Glucose-6-Phosphate Dehydrogenase Deficiency in Brazilian Children With Sickle Cell Anemia is not Associated With Clinical Ischemic Stroke or High-Risk Transcranial Doppler
Published in Pediatric blood & cancer (01-06-2016)“…Background Stroke is a severe complication of sickle cell anemia (SCA). The role of glucose‐6‐phosphate dehydrogenase (G6PD) deficiency in the development of…”
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12
The Renin Angiotensin System and Bipolar Disorder: A Systematic Review
Published in Protein and peptide letters (01-01-2020)“…Bipolar Disorder (BD) is a chronic a multifactorial psychiatric illness that affects mood, cognition, and functioning. BD is associated with several…”
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13
Genetic, laboratory and clinical risk factors in the development of overt ischemic stroke in children with sickle cell disease
Published in Hematology, Transfusion and Cell Therapy (01-04-2018)“…Cerebrovascular disease, particularly stroke, is one of the most severe clinical complications associated with sickle cell disease and is a significant cause…”
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14
Association between inflammatory molecules, nitric oxide metabolites and leg ulcers in individuals with sickle cell anemia
Published in Hematology, Transfusion and Cell Therapy (01-04-2022)“…Leg ulcers (LUs) are relatively common in patients with sickle cell anemia (SCA). The role of inflammation and nitric oxide (NO) pathways in the…”
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15
Glucocorticoid receptor Gene (NR3C1) Polymorphisms and Haplotypes in patients with congenital adrenal hyperplasia
Published in Molecular and cellular endocrinology (01-10-2021)“…Lifelong glucocorticoid (GC) replacement is the mainstay treatment of congenital adrenal hyperplasia (CAH) due to classic 21-hydroxylase deficiency (21-OHD)…”
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16
Alpha-thalassemia protects against cerebrovascular disease in children with sickle cell anemia
Published in Arquivos de neuro-psiquiatria (01-08-2012)Get full text
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Estimated glomerular filtration rate in Brazilian adults with sickle cell disease: results from the REDS-III multicenter cohort study
Published in Annals of hematology (01-05-2023)“… Chronic kidney disease (CKD) has a significant impact on sickle cell disease (SCD) morbidity and mortality. Early identification of individuals at highest…”
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Association between ENPP1 K173Q and stroke in a newborn cohort of 395 Brazilian children with sickle cell anemia
Published in Blood (03-09-2015)Get full text
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Evaluation of insertion/deletion (I/D) polymorphisms of ACE gene and circulating levels of angiotensin II in congenital anomalies of the kidney and urinary tract
Published in Molecular biology reports (01-06-2022)“…Background Congenital Anomalies of the Kidney and the Urinary Tract (CAKUT) are defined as a heterogeneous group of anomalies that resulted from defects in…”
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Natural history of albuminuria in a large cohort of children and adolescents with sickle cell anemia from Brazil
Published in Blood advances (23-01-2024)Get full text
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