Lista de obras - Marcos Borato Viana - Dominio Público Uruguay

30 Years of Experience with Non-Hodgkin Lymphoma in Children and Adolescents: a retrospective cohort study

artículo científico publicado en 2020

Alpha chain hemoglobins with electrophoretic mobility similar to that of hemoglobin S in a newborn screening program.

artículo científico publicado en 2013

Alpha-thalassemia should be considered in the differential diagnosis of a child with anemia

artículo científico publicado en 2011

Anemia and infection: a complex relationship

artículo científico publicado en 2011

Association between ENPP1 K173Q and stroke in a newborn cohort of 395 Brazilian children with sickle cell anemia

artículo científico publicado en 2015

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

artículo científico publicado en 2014

Characterization of mortality in children with sickle cell disease diagnosed through the Newborn Screening Program.

artículo científico publicado en 2014

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

artículo científico publicado en 2012

Clinical complications in pregnant women with sickle cell disease: prospective study of factors predicting maternal death or near miss

artículo científico publicado en 2014

Clinical course and prognostic factors of children with Burkitt's lymphoma in a developing country: the experience of a single centre in Brazil

artículo científico publicado en 2012

Cognitive profile of children with sickle cell anemia compared to healthy controls

artículo científico publicado en 2018

Coinheritance of α-thalassemia decreases the risk of cerebrovascular disease in a cohort of children with sickle cell anemia

artículo científico publicado en 2010

Community healthcare workers' perception of an educational intervention in the care of patients with sickle cell disease in Brazil

artículo científico publicado en 2015

Comparison between qualitative and real-time polymerase chain reaction to evaluate minimal residual disease in children with acute lymphoblastic leukemia

artículo científico publicado en 2015

Data with unexpected values should be checked

scientific article published on 01 January 2008

De novo acute myeloid leukemia in adults younger than 60 years of age: socioeconomic aspects and treatment results in a Brazilian university center

scientific article published on 01 August 2006

De novo alpha 2 hemoglobin gene (HBA2) mutation in a child with hemoglobin M Iwate and symptomatic methemoglobinemia since birth

artículo científico publicado en 2014

Effectiveness of an educational programme about sickle cell disease in the form of active methodologies among community health agents and nursing technicians of primary care in Minas Gerais, Brazil

article

Etoposide in the treatment of six children with Langerhans cell histiocytosis (histiocytosis X)

artículo científico publicado en 1991

Frequency of biotinidase gene variants and incidence of biotinidase deficiency in the Newborn Screening Program in Minas Gerais, Brazil

scientific article published on 04 December 2019

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

scientific article published on 23 May 2020

Further studies on erythrocyte thiamin transport and phosphorylation in seven patients with thiamin-responsive megaloblastic anaemia

artículo científico publicado en 1994

Gene rearrangement study for minimal residual disease monitoring in children with acute lymphocytic leukemia

artículo científico publicado en 2013

Growth deficits in children with sickle cell disease

artículo científico publicado en 2002

Hb Etobicoke mutation in a hybrid HBA212 allele [HBA212 84 (F5) Ser>Arg; HBA212:c.255C>G].

artículo científico publicado en 2012

Hb Stanleyville-II [α78(EF7)Asn→Lys (α2); HbA2: c.237C>A]: incidence of 1:11,500 in a newborn screening program in Brazil

artículo científico publicado en 2012

Health-related quality of life among teenagers during cancer treatment in a developing country: patients' and proxies' reports

artículo científico publicado en 2013

Height deficit and impairment of the GH/IGF-1 axis in patients treated for acute lymphoblastic leukemia during childhood

artículo científico publicado en 2013

Height deficit during and many years after treatment for acute lymphoblastic leukemia in children: a review.

artículo científico publicado en 2008

Hemophagocytic lymphohistiocytosis: a case series of a Brazilian institution

artículo científico publicado en 2014

High Incidence of Biotinidase Deficiency from a Pilot Newborn Screening Study in Minas Gerais, Brazil.

artículo científico publicado en 2015

High reticulocyte count is an independent risk factor for cerebrovascular disease in children with sickle cell anemia

artículo científico publicado en 2010

Homozygous Hb Stanleyville-II [alpha2 78(EF7) Asn>Lys; HBA2:c.237C>A, not C>G] associated with genotype −α3.7/−α3.7 in two Brazilian families

article

Immunophenotyping of the cerebrospinal fluid as a prognostic factor at diagnosis of acute lymphoblastic leukemia in children and adolescents

artículo científico publicado en 2017

Incidence and risk factors for central nervous system relapse in children and adolescents with acute lymphoblastic leukemia.

artículo científico publicado en 2012

Inefficacy of piracetam in the prevention of painful crises in children and adolescents with sickle cell disease

artículo científico publicado en 2005

Iron deficiency in Brazilian infants with sickle cell disease.

artículo científico publicado en 2011

Kaplan-Meier method is inappropriate for estimating cumulative incidence of graft-versus-host disease in the presence of competing events

artículo científico publicado en 2010

Lack of association between N-ras gene mutations and clinical prognosis in Brazilian children with acute lymphoblastic leukemia

artículo científico publicado en 2001

Langerhans cell histiocytosis: a 16-year experience

artículo científico publicado en 2007

Longitudinal growth and risk factors for growth deficiency in children treated for acute lymphoblastic leukemia

artículo científico publicado en 2007

Minimal residual disease in cerebrospinal fluid at diagnosis: a more intensive treatment protocol was able to eliminate the adverse prognosis in children with acute lymphoblastic leukemia

artículo científico publicado en 2011

Mortality of children with sickle cell disease: a population study

artículo científico publicado en 2010

Negative prognostic impact of PTEN mutation in pediatric T-cell acute lymphoblastic leukemia

artículo científico publicado en 2009

Novel mutations causing biotinidase deficiency in individuals identified by the newborn screening program in Minas Gerais, Brazil

scientific article published on 26 March 2019

Outcome of children and adolescents with lymphoblastic lymphoma.

artículo científico publicado en 2016

Perception of primary care doctors and nurses about care provided to sickle cell disease patients

artículo científico publicado en 2015

Pregnancy in patients with sickle cell disease: maternal and perinatal outcomes

artículo científico publicado en 2014

Prevalence and incidence of erythrovirus B19 infection in children with sickle cell disease: The impact of viral infection in acute clinical events.

artículo científico publicado en 2015

Reliability of isoelectrofocusing for the detection of Hb S, Hb C, and HB D in a pioneering population-based program of newborn screening in Brazil

artículo científico publicado en 2001

Sickle cell disease: a clinical and histopathologic study of the liver in living children

artículo científico publicado en 2002

Subclassification of acute lymphoblastic leukaemia in children: analysis of the reproducibility of morphological criteria and prognostic implications

scientific article published on 01 March 1980

Survival of children with sickle cell disease in the comprehensive newborn screening programme in Minas Gerais, Brazil

artículo científico publicado en 2015

The Natural History of Hb S/Hereditary Persistence of Fetal Hemoglobin in 13 Children from the State of Minas Gerais, Brazil.

artículo científico publicado en 2016

The invisibility of sickle cell disease in Brazil: lessons from a study in Maranhão

artículo científico publicado en 2014

Thiamine-responsive megaloblastic anemia, sensorineural deafness, and diabetes mellitus: A new syndrome?

artículo científico publicado en 1978

Thiopurine S-methyltransferase (TPMT) gene polymorphism in Brazilian children with acute lymphoblastic leukemia: association with clinical and laboratory data

artículo científico publicado en 2008

Unstable hemoglobin Rush [beta 101(G3) Glu>Gln, HBB:c.304G>C] in a Brazilian family with moderate hemolytic anemia

artículo científico publicado en 2012

Very mild forms of Hb S/beta(+)-thalassemia in Brazilian children

artículo científico publicado en 2015

β-Globin Gene Cluster Haplotypes in a Cohort of 221 Children with Sickle Cell Anemia or Sβ&#8304;-Thalassemia and Their Association with Clinical and Hematological Features ⬇️

artículo científico publicado el 12 de octubre de 2010

Lista de obras de Marcos Borato Viana

30 Years of Experience with Non-Hodgkin Lymphoma in Children and Adolescents: a retrospective cohort study

Alpha chain hemoglobins with electrophoretic mobility similar to that of hemoglobin S in a newborn screening program.

Alpha-thalassemia should be considered in the differential diagnosis of a child with anemia

Anemia and infection: a complex relationship

Association between ENPP1 K173Q and stroke in a newborn cohort of 395 Brazilian children with sickle cell anemia

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

Characterization of mortality in children with sickle cell disease diagnosed through the Newborn Screening Program.

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

Clinical complications in pregnant women with sickle cell disease: prospective study of factors predicting maternal death or near miss

Clinical course and prognostic factors of children with Burkitt's lymphoma in a developing country: the experience of a single centre in Brazil

Cognitive profile of children with sickle cell anemia compared to healthy controls

Coinheritance of α-thalassemia decreases the risk of cerebrovascular disease in a cohort of children with sickle cell anemia

Community healthcare workers' perception of an educational intervention in the care of patients with sickle cell disease in Brazil

Comparison between qualitative and real-time polymerase chain reaction to evaluate minimal residual disease in children with acute lymphoblastic leukemia

Data with unexpected values should be checked

De novo acute myeloid leukemia in adults younger than 60 years of age: socioeconomic aspects and treatment results in a Brazilian university center

De novo alpha 2 hemoglobin gene (HBA2) mutation in a child with hemoglobin M Iwate and symptomatic methemoglobinemia since birth

Effectiveness of an educational programme about sickle cell disease in the form of active methodologies among community health agents and nursing technicians of primary care in Minas Gerais, Brazil

Etoposide in the treatment of six children with Langerhans cell histiocytosis (histiocytosis X)

Frequency of biotinidase gene variants and incidence of biotinidase deficiency in the Newborn Screening Program in Minas Gerais, Brazil

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

Further studies on erythrocyte thiamin transport and phosphorylation in seven patients with thiamin-responsive megaloblastic anaemia

Gene rearrangement study for minimal residual disease monitoring in children with acute lymphocytic leukemia

Growth deficits in children with sickle cell disease

Hb Etobicoke mutation in a hybrid HBA212 allele [HBA212 84 (F5) Ser>Arg; HBA212:c.255C>G].

Hb Stanleyville-II [α78(EF7)Asn→Lys (α2); HbA2: c.237C>A]: incidence of 1:11,500 in a newborn screening program in Brazil

Health-related quality of life among teenagers during cancer treatment in a developing country: patients' and proxies' reports

Height deficit and impairment of the GH/IGF-1 axis in patients treated for acute lymphoblastic leukemia during childhood

Height deficit during and many years after treatment for acute lymphoblastic leukemia in children: a review.

Hemophagocytic lymphohistiocytosis: a case series of a Brazilian institution

High Incidence of Biotinidase Deficiency from a Pilot Newborn Screening Study in Minas Gerais, Brazil.

High reticulocyte count is an independent risk factor for cerebrovascular disease in children with sickle cell anemia

Homozygous Hb Stanleyville-II [alpha2 78(EF7) Asn>Lys; HBA2:c.237C>A, not C>G] associated with genotype −α3.7/−α3.7 in two Brazilian families

Immunophenotyping of the cerebrospinal fluid as a prognostic factor at diagnosis of acute lymphoblastic leukemia in children and adolescents

Incidence and risk factors for central nervous system relapse in children and adolescents with acute lymphoblastic leukemia.

Inefficacy of piracetam in the prevention of painful crises in children and adolescents with sickle cell disease

Iron deficiency in Brazilian infants with sickle cell disease.

Kaplan-Meier method is inappropriate for estimating cumulative incidence of graft-versus-host disease in the presence of competing events

Lack of association between N-ras gene mutations and clinical prognosis in Brazilian children with acute lymphoblastic leukemia

Langerhans cell histiocytosis: a 16-year experience

Longitudinal growth and risk factors for growth deficiency in children treated for acute lymphoblastic leukemia

Minimal residual disease in cerebrospinal fluid at diagnosis: a more intensive treatment protocol was able to eliminate the adverse prognosis in children with acute lymphoblastic leukemia

Mortality of children with sickle cell disease: a population study

Negative prognostic impact of PTEN mutation in pediatric T-cell acute lymphoblastic leukemia

Novel mutations causing biotinidase deficiency in individuals identified by the newborn screening program in Minas Gerais, Brazil

Outcome of children and adolescents with lymphoblastic lymphoma.

Perception of primary care doctors and nurses about care provided to sickle cell disease patients

Pregnancy in patients with sickle cell disease: maternal and perinatal outcomes

Prevalence and incidence of erythrovirus B19 infection in children with sickle cell disease: The impact of viral infection in acute clinical events.

Reliability of isoelectrofocusing for the detection of Hb S, Hb C, and HB D in a pioneering population-based program of newborn screening in Brazil

Sickle cell disease: a clinical and histopathologic study of the liver in living children

Subclassification of acute lymphoblastic leukaemia in children: analysis of the reproducibility of morphological criteria and prognostic implications

Survival of children with sickle cell disease in the comprehensive newborn screening programme in Minas Gerais, Brazil

The Natural History of Hb S/Hereditary Persistence of Fetal Hemoglobin in 13 Children from the State of Minas Gerais, Brazil.

The invisibility of sickle cell disease in Brazil: lessons from a study in Maranhão

Thiamine-responsive megaloblastic anemia, sensorineural deafness, and diabetes mellitus: A new syndrome?

Thiopurine S-methyltransferase (TPMT) gene polymorphism in Brazilian children with acute lymphoblastic leukemia: association with clinical and laboratory data

Unstable hemoglobin Rush [beta 101(G3) Glu>Gln, HBB:c.304G>C] in a Brazilian family with moderate hemolytic anemia

Very mild forms of Hb S/beta(+)-thalassemia in Brazilian children

β-Globin Gene Cluster Haplotypes in a Cohort of 221 Children with Sickle Cell Anemia or Sβ&amp;#8304;-Thalassemia and Their Association with Clinical and Hematological Features ⬇️

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 ⬇️