Detalhe da pesquisa
1.
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.
J Hum Genet;
67(12): 701-709, 2022 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36167770
2.
Evidence for interactions between inflammatory markers and renin-angiotensin system molecules in the occurrence of albuminuria in children with sickle cell anemia.
Cytokine;
125: 154800, 2020 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31442679
3.
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.
Ann Hematol;
99(7): 1453-1463, 2020 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32447424
4.
Severe clinical picture in a cohort of six Brazilian children with hemoglobin Sß-thalassemia IVS-I-5 G>A.
Blood Cells Mol Dis;
104: 102795, 2024 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37660418
5.
Immunophenotyping of the cerebrospinal fluid as a prognostic factor at diagnosis of acute lymphoblastic leukemia in children and adolescents.
Pediatr Hematol Oncol;
34(2): 53-65, 2017 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28548878
6.
Prevalence and incidence of erythrovirus B19 infection in children with sickle cell disease: The impact of viral infection in acute clinical events.
J Med Virol;
88(4): 588-95, 2016 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26369294
7.
Reticulocyte count is the most important predictor of acute cerebral ischemia and high-risk transcranial Doppler in a newborn cohort of 395 children with sickle cell anemia.
Ann Hematol;
95(11): 1869-80, 2016 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27520094
8.
The Natural History of Hb S/Hereditary Persistence of Fetal Hemoglobin in 13 Children from the State of Minas Gerais, Brazil.
Hemoglobin;
40(3): 215-9, 2016 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27117574
9.
Association of alpha-thalassemia, TNF-alpha (-308G>A) and VCAM-1 (c.1238G>C) gene polymorphisms with cerebrovascular disease in a newborn cohort of 411 children with sickle cell anemia.
Blood Cells Mol Dis;
54(1): 44-50, 2015 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25175566
10.
Prevalence and risk factors for albuminuria and glomerular hyperfiltration in a large cohort of children with sickle cell anemia.
Am J Hematol;
95(5): E125-E128, 2020 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32083326
11.
Health-related quality of life among teenagers during cancer treatment in a developing country: patients' and proxies' reports.
Pediatr Hematol Oncol;
30(4): 307-16, 2013 May.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23574300
12.
Clinical, laboratory, and molecular characteristics of a cohort of children with hemoglobinopathy S/beta-thalassemia.
Hematol Transfus Cell Ther;
2023 Dec 19.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38182466
13.
Association between ENPP1 K173Q and stroke in a newborn cohort of 395 Brazilian children with sickle cell anemia.
Blood;
126(10): 1259-60, 2015 Sep 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26337355
14.
Unstable hemoglobin Rush [beta 101(G3) Glu>Gln, HBB:c.304G>C] in a Brazilian family with moderate hemolytic anemia.
Ann Hematol;
91(7): 1091-6, 2012 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22273838
15.
Hb Stanleyville-II [α78(EF7)AsnâLys (α2); HbA2: c.237C>A]: incidence of 1:11,500 in a newborn screening program in Brazil.
Hemoglobin;
36(4): 388-94, 2012.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22625430
16.
Follow-up of children with sickle cell anemia screened with transcranial Doppler and enrolled in a primary prevention program of ischemic stroke.
Hematol Transfus Cell Ther;
44(4): 478-484, 2022.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34210619
17.
High reticulocyte count is an independent risk factor for cerebrovascular disease in children with sickle cell anemia.
Pediatr Blood Cancer;
56(1): 116-21, 2011 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20949593
18.
ß-globin gene cluster haplotypes in a cohort of 221 children with sickle cell anemia or Sß°-thalassemia and their association with clinical and hematological features.
Acta Haematol;
124(3): 162-70, 2010.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20938172
19.
Coinheritance of α-thalassemia decreases the risk of cerebrovascular disease in a cohort of children with sickle cell anemia.
Hemoglobin;
34(6): 516-29, 2010.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21077759
20.
Frequency of biotinidase gene variants and incidence of biotinidase deficiency in the Newborn Screening Program in Minas Gerais, Brazil.
J Med Screen;
27(3): 115-120, 2020 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31801038