Lista de obras - Elvira Deolinda Velloso - Dominio Público Uruguay

A Novel Assay for the Identification of NOTCH1 PEST Domain Mutations in Chronic Lymphocytic Leukemia

artículo científico publicado en 2016

A novel 60 kDa reactivity in cyclic neutropenia: high titer cytoplasmic ANCA immunostaining pattern and negative anti-proteinase-3 antibody

scientific article published on 19 November 2010

Acute myeloid leukemia with e1a2 BCR-ABL1 fusion gene: two cases with peculiar molecular and clinical presentations.

artículo científico publicado en 2017

Array-CGH as an adjuvant tool in cytogenetic diagnosis of pediatric MDS and JMML.

artículo científico publicado en 2013

Bone marrow findings in systemic lupus erythematosus patients with peripheral cytopenias.

artículo científico publicado en 1998

Correlation between flow cytometry and histologic findings: ten year experience in the investigation of lymphoproliferative diseases

artículo científico publicado en 2011

Deletion of RUNX1 exons 1 and 2 associated with familial platelet disorder with propensity to acute myeloid leukemia

scientific article published on 05 February 2018

Deletions of the long arm of chromosome 7 in myeloid disorders: loss of band 7q32 implies worst prognosis

artículo científico publicado en 1996

Detection of cytogenetic abnormalities in mature B-cell neoplasms: the value of cultures with different mitogens.

artículo científico publicado en 2014

Duffy null genotype or Fy(a-b-) phenotype are more accurate than self-declared race for diagnosing benign ethnic neutropenia in Brazilian population.

artículo científico publicado en 2017

Eosinophil chimerism in the differential diagnosis between DEK-NUP214-positive acute myeloid leukaemia relapse and chronic graft-versus-host disease

artículo científico publicado en 2015

Evaluation of chromosomal abnormalities by cIg-FISH and association with proliferative and apoptotic indexes in multiple myeloma.

scientific article published on 23 August 2012

Homozygous loss of function BRCA1 variant causing a Fanconi-anemia-like phenotype, a clinical report and review of previous patients.

artículo científico publicado en 2017

Identification of ANLN as ETV6 partner gene in recurrent t(7;12)(p15;p13): a possible role of deregulated ANLN expression in leukemogenesis.

artículo científico publicado en 2015

Identification of a novel fusion TBL1XR1-PDGFRB in a patient with acute myeloid leukemia harboring the DEK-NUP214 fusion and clinical response to dasatinib.

artículo científico publicado en 2017

Immunohematological findings in myelodysplastic syndrome

artículo científico publicado en 2001

Incidence and risk factors of aplastic anemia in Latin American countries: the LATIN case-control study

artículo científico publicado en 2009

MDR-1 and GST polymorphisms are involved in myelodysplasia progression.

artículo científico publicado en 2013

Megakaryocyte

artículo científico publicado en 2011

Molecular and cytogenetic abnormalities in acute myeloid leukemia: review and case studies

artículo científico publicado en 2011

Molecular genetic techniques for gains and losses of genomic material in a case of acute myeloid leukemia.

artículo científico publicado en 2017

Myelodysplastic syndromes in South America: a multinational study of 1080 patients

artículo científico publicado en 2015

Possible benefit of consolidation therapy with high-dose cytarabine on overall survival of adults with non-promyelocytic acute myeloid leukemia

artículo científico publicado en 2014

Pre-analytical parameters associated with unsuccessful karyotyping in myeloid neoplasm: a study of 421 samples

scientific article published on 14 February 2019

Salvage treatment for refractory or relapsed acute myeloid leukemia: a 10-year single-center experience

artículo científico publicado en 2020

Scientific comment on tumor suppressor p53 protein expression: prognostic significance in patients with low-risk myelodysplastic syndrome

artículo científico publicado en 2014

Secondary myeloid neoplasms: bone marrow cytogenetic and histological features may be relevant to prognosis.

artículo científico publicado en 2016

Single-nucleotide polymorphism array (SNP-A) improves the identification of chromosomal abnormalities by metaphase cytogenetics in myelodysplastic syndrome.

artículo científico publicado en 2016

The Brazilian Pediatric Myelodysplastic Cooperative Group strategies: are they relevant to improve educational approach and correct diagnosis?

artículo científico publicado en 2002

The detection of KIT mutations in acute myeloid leukemia.

artículo científico publicado en 2012

Translocation t(8;16)(p11;p13) in acute non-lymphocytic leukemia: report on two new cases and review of the literature.

artículo científico publicado en 1996

Treating Adult Acute Lymphoblastic Leukemia in Brazil-Increased Early Mortality Using a German Multicenter Acute Lymphoblastic Leukemia-based regimen.

artículo científico publicado en 2018

Treatment of pediatric myelodysplastic syndromes and juvenile myelomonocytic leukemia: the Brazilian experience in the past decade.

artículo científico publicado en 2004

Validation of interphase fluorescence in situ hybridization (iFISH) for multiple myeloma using CD138 positive cells

artículo científico publicado en 2016

Lista de obras de Elvira Deolinda Velloso

A Novel Assay for the Identification of NOTCH1 PEST Domain Mutations in Chronic Lymphocytic Leukemia

A novel 60 kDa reactivity in cyclic neutropenia: high titer cytoplasmic ANCA immunostaining pattern and negative anti-proteinase-3 antibody

Acute myeloid leukemia with e1a2 BCR-ABL1 fusion gene: two cases with peculiar molecular and clinical presentations.

Array-CGH as an adjuvant tool in cytogenetic diagnosis of pediatric MDS and JMML.

Bone marrow findings in systemic lupus erythematosus patients with peripheral cytopenias.

Correlation between flow cytometry and histologic findings: ten year experience in the investigation of lymphoproliferative diseases

Deletion of RUNX1 exons 1 and 2 associated with familial platelet disorder with propensity to acute myeloid leukemia

Deletions of the long arm of chromosome 7 in myeloid disorders: loss of band 7q32 implies worst prognosis

Detection of cytogenetic abnormalities in mature B-cell neoplasms: the value of cultures with different mitogens.

Duffy null genotype or Fy(a-b-) phenotype are more accurate than self-declared race for diagnosing benign ethnic neutropenia in Brazilian population.

Eosinophil chimerism in the differential diagnosis between DEK-NUP214-positive acute myeloid leukaemia relapse and chronic graft-versus-host disease

Evaluation of chromosomal abnormalities by cIg-FISH and association with proliferative and apoptotic indexes in multiple myeloma.

Homozygous loss of function BRCA1 variant causing a Fanconi-anemia-like phenotype, a clinical report and review of previous patients.

Identification of ANLN as ETV6 partner gene in recurrent t(7;12)(p15;p13): a possible role of deregulated ANLN expression in leukemogenesis.

Identification of a novel fusion TBL1XR1-PDGFRB in a patient with acute myeloid leukemia harboring the DEK-NUP214 fusion and clinical response to dasatinib.

Immunohematological findings in myelodysplastic syndrome

Incidence and risk factors of aplastic anemia in Latin American countries: the LATIN case-control study

MDR-1 and GST polymorphisms are involved in myelodysplasia progression.

Megakaryocyte

Molecular and cytogenetic abnormalities in acute myeloid leukemia: review and case studies

Molecular genetic techniques for gains and losses of genomic material in a case of acute myeloid leukemia.

Myelodysplastic syndromes in South America: a multinational study of 1080 patients

Possible benefit of consolidation therapy with high-dose cytarabine on overall survival of adults with non-promyelocytic acute myeloid leukemia

Pre-analytical parameters associated with unsuccessful karyotyping in myeloid neoplasm: a study of 421 samples

Salvage treatment for refractory or relapsed acute myeloid leukemia: a 10-year single-center experience

Scientific comment on tumor suppressor p53 protein expression: prognostic significance in patients with low-risk myelodysplastic syndrome

Secondary myeloid neoplasms: bone marrow cytogenetic and histological features may be relevant to prognosis.

Single-nucleotide polymorphism array (SNP-A) improves the identification of chromosomal abnormalities by metaphase cytogenetics in myelodysplastic syndrome.

The Brazilian Pediatric Myelodysplastic Cooperative Group strategies: are they relevant to improve educational approach and correct diagnosis?

The detection of KIT mutations in acute myeloid leukemia.

Translocation t(8;16)(p11;p13) in acute non-lymphocytic leukemia: report on two new cases and review of the literature.

Treating Adult Acute Lymphoblastic Leukemia in Brazil-Increased Early Mortality Using a German Multicenter Acute Lymphoblastic Leukemia-based regimen.

Treatment of pediatric myelodysplastic syndromes and juvenile myelomonocytic leukemia: the Brazilian experience in the past decade.

Validation of interphase fluorescence in situ hybridization (iFISH) for multiple myeloma using CD138 positive cells