about
Thiopurine S-methyltransferase (TPMT) gene polymorphism in Brazilian children with acute lymphoblastic leukemia: association with clinical and laboratory data.Hemophagocytic lymphohistiocytosis: a case series of a Brazilian institution.Clinical complications in pregnant women with sickle cell disease: prospective study of factors predicting maternal death or near missThe invisibility of sickle cell disease in Brazil: lessons from a study in MaranhãoCommunity healthcare workers' perception of an educational intervention in the care of patients with sickle cell disease in Brazil.High Incidence of Biotinidase Deficiency from a Pilot Newborn Screening Study in Minas Gerais, Brazil.Clinical course and prognostic factors of children with Burkitt's lymphoma in a developing country: the experience of a single centre in BrazilIncidence and risk factors for central nervous system relapse in children and adolescents with acute lymphoblastic leukemia.Height deficit during and many years after treatment for acute lymphoblastic leukemia in children: a review.Gene rearrangement study for minimal residual disease monitoring in children with acute lymphocytic leukemiaThe Natural History of Hb S/Hereditary Persistence of Fetal Hemoglobin in 13 Children from the State of Minas Gerais, Brazil.Survival of children with sickle cell disease in the comprehensive newborn screening programme in Minas Gerais, Brazil.Prevalence and incidence of erythrovirus B19 infection in children with sickle cell disease: The impact of viral infection in acute clinical events.Perception of primary care doctors and nurses about care provided to sickle cell disease patients.Outcome of children and adolescents with lymphoblastic lymphoma.Alpha chain hemoglobins with electrophoretic mobility similar to that of hemoglobin S in a newborn screening program.Characterization of mortality in children with sickle cell disease diagnosed through the Newborn Screening Program.Comparison between qualitative and real-time polymerase chain reaction to evaluate minimal residual disease in children with acute lymphoblastic leukemiaAnemia and infection: a complex relationship.Very mild forms of Hb S/beta(+)-thalassemia in Brazilian children.De novo alpha 2 hemoglobin gene (HBA2) mutation in a child with hemoglobin M Iwate and symptomatic methemoglobinemia since birthThiamine-responsive megaloblastic anemia, sensorineural deafness, and diabetes mellitus: A new syndrome?Kaplan-Meier method is inappropriate for estimating cumulative incidence of graft-versus-host disease in the presence of competing events.Pregnancy in patients with sickle cell disease: maternal and perinatal outcomes.Lack of association between N-ras gene mutations and clinical prognosis in Brazilian children with acute lymphoblastic leukemia.Height deficit and impairment of the GH/IGF-1 axis in patients treated for acute lymphoblastic leukemia during childhood.Sickle cell disease: a clinical and histopathologic study of the liver in living children.Coinheritance of α-thalassemia decreases the risk of cerebrovascular disease in a cohort of children with sickle cell anemia.Etoposide in the treatment of six children with Langerhans cell histiocytosis (histiocytosis X)Health-related quality of life among teenagers during cancer treatment in a developing country: patients' and proxies' reports.Clinical and molecular characterization of hemoglobin Maputo [beta 47 (CD6) Asp > Tyr HBB: c.142G > T] and G-Ferrara [beta 57 (E1) Asn > Lys HBB: c.174C > A] in a newborn screening in Brazil.Mortality of children with sickle cell disease: a population study.Inefficacy of piracetam in the prevention of painful crises in children and adolescents with sickle cell disease.Hb Etobicoke mutation in a hybrid HBA212 allele [HBA212 84 (F5) Ser>Arg; HBA212:c.255C>G].Iron deficiency in Brazilian infants with sickle cell disease.β-globin gene cluster haplotypes in a cohort of 221 children with sickle cell anemia or Sβ⁰-thalassemia and their association with clinical and hematological features.Association between ENPP1 K173Q and stroke in a newborn cohort of 395 Brazilian children with sickle cell anemia.Immunophenotyping of the cerebrospinal fluid as a prognostic factor at diagnosis of acute lymphoblastic leukemia in children and adolescents.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.Hb Stanleyville-II [α78(EF7)Asn→Lys (α2); HbA2: c.237C>A]: incidence of 1:11,500 in a newborn screening program in Brazil.
P50
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P50
description
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հետազոտող
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name
Marcos Borato Viana
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Marcos Borato Viana
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Marcos Borato Viana
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Marcos Borato Viana
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Marcos Borato Viana
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label
Marcos Borato Viana
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Marcos Borato Viana
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Marcos Borato Viana
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Marcos Borato Viana
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Marcos Borato Viana
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Marcos Borato Viana
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Marcos Borato Viana
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Marcos Borato Viana
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Marcos Borato Viana
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Marcos Borato Viana
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Marcos Borato Viana
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P1053
E-8415-2010
P106
P21
P31
P3829
P496
0000-0001-9665-2115