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Results 11-20 of 25 (Search time: 0.003 seconds).
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Issue DateTitleAuthor(s)
2016NQO1, GSTM1 and GSTT1 variants are associated with pediatric acute myeloid leukemia with genetic abnormalitiesBrisson, Gisele Dallapicola; Andrade, Francianne Gomes; Bueno, Filipe Vicente dos Santos; Lopes, Bruno de Almeida; Gonçalves, Bruno Alves de Aguiar; Pina, Eugênia Terra Granado; Pombo-de-Oliveira, Maria do Socorro
2016NQO1, GSTM1 and GSTT1 polymorphisms are associated with childhood acute myeloid leukemia subtypes and type i mutationsBrisson, Gisele Dallapicola; Andrade, Francianne Gomes; Bueno, Filipe Vicente dos Santos; Sardou-Cezar, Ingrid; Lopes, Bruno de Almeida; Gonçalves, Bruno Alves de Aguiar; Pina, Eugênia Terra Granado; Pombo-de-Oliveira, Maria do Socorro
2016Molecular characterization of pediatric acute myeloid leukemia in Brazil: perspectives of a multicentric studyAndrade, Francianne Gomes; Brisson, Gisele Dallapicola; Bueno, Filipe Vicente dos Santos; Sardou-Cezar, Ingrid; Feliciano, Suellen Valadares Moura; Pina, Eugênia Terra Granado; Noronha, Elda Pereira; Pombo-de-Oliveira, Maria do Socorro
2017Molecular characterization of pediatric acute myeloid leukemiaAndrade, Francianne Gomes; Sardou-Cezar, Ingrid; Bueno, Filipe Vicente dos Santos; Brisson, Gisele Dallapicola; Pina, Eugênia Terra Granado; Noronha, Elda Pereira; Pombo-de-Oliveira, Maria do Socorro
2018The identification of PTPN11 mutations in pediatric myeloid neoplasms in BrazilBueno, Filipe Vicente dos Santos; Andrade, Francianne Gomes; Noronha, Elda Pereira; Pina, Eugênia Terra Granado; Sardou-Cezar, Ingrid; Chung Filho, Alython Araujo; Brisson, Gisele Dallapicola; Almeida, Daniela Palheiro Mendes de; Pombo-de-Oliveira, Maria do Socorro
2018Molecular alterations in rare subsets of pediatric acute myeloid leukemiaAndrade, Francianne Gomes; Sardou-Cezar, Ingrid; Bueno, Filipe Vicente dos Santos; Marques, Luísa Vieira Codeço; Brisson, Gisele Dallapicola; Pina, Eugênia Terra Granado; Noronha, Elda Pereira; Pombo-de-Oliveira, Maria do Socorro
2019-05T-lymphoid/myeloid mixed phenotype acute leukemia and early T-cell precursor lymphoblastic leukemia similarities with NOTCH1 mutation as a good prognostic factorNoronha, Elda Pereira; Marques, Luísa Vieira Codeço; Andrade, Francianne Gomes; Sardou-Cezar, Ingrid; Bueno, Filipe Vicente dos Santos; Zampier, Carolina da Paz; Pina, Eugênia Terra Granado; Pombo-de-Oliveira, Maria do Socorro
2017Immuno-molecular profile of pediatric acute leukemia with aberrant myeloid and t phenotype and its impact on the event-free survivalNoronha, Elda Pereira; Marques, Luísa Vieira Codeço; Andrade, Francianne Gomes; Barbosa, Thayana da Conceição; Brisson, Gisele Dallapicola; Sardou-Cezar, Ingrid; Bueno, Filipe Vicente dos Santos; Zampier, Carolina da Paz; Mansur, Marcela Braga; Pina, Eugênia Terra Granado; Pombo-de-Oliveira, Maria do Socorro
2019Detection of gata2 mutations in patients with nontuberculous mycobacterial or fungal infections without known immunodeficiency in Rio de Janeiro,BrazilAlmeida, Daniela Palheiro Mendes de; Bueno, Filipe Vicente dos Santos; Andrade, Francianne Gomes; Freitas, Dayvison F.rancis Saraiva; Oliveira, Rosely Maria Zancopé; Pombo-de-Oliveira, Maria do Socorro
2020-06Myelodysplastic syndrome with clonal karyotype evolution associated with trisomy 8 and ASXL1 mutation in well-controlled HIV patient: Case report and literature review.Almeida, Daniela Palheiro Mendes de; Lovatel, Viviane Lamim; Bueno, Filipe Vicente dos Santos; Kós, Elaiza Almeida Antônio de; Andrade, Francianne Gomes; Grinsztejn, Beatriz Gilda J; Pombo-de-Oliveira, Maria do Socorro; Fernandez, Teresa de Souza

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