Secondary abnormalities involving 1q or 13q and poor outcome in high stage Burkitt leukemia/lymphoma cases with 8q24 rearrangement at diagnosis
de Souza, Mariana Tavares, Mkrtchyan, Hasmik, Hassan, Rocio, Ney-Garcia, Daniela Ribeiro, de Azevedo, Alice Maria Boulhosa, da Costa, Elaine Sobral, de Figueiredo, Amanda Faria, Liehr, Thomas, Abdelhay, Eliana, Silva, Maria Luiza Macedo
Published in International journal of hematology (01.02.2011)
Published in International journal of hematology (01.02.2011)
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Childhood B-cell progenitor acute lymphoblastic leukemia presenting a three-way t(11;12;21)(q14;p13;q22) with a RUNX1 gene signal on chromosome 11
Ney-Garcia, D. R., Liehr, T., Bhatt, S., de Souza, M. T., de Matos, R. R. Capela, Pimenta, G., Pulcheri, W., Ribeiro, R. C., Abdelhay, E., Silva, Maria Luiza Macedo
Published in International journal of hematology (2012)
Published in International journal of hematology (2012)
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An uncommon t(9;11)(p24;q22) with monoallelic loss of ATM and KMT2A genes in a child with myelodysplastic syndrome/acute myeloid leukemia who evolved from Fanconi anemia
Lovatel, Viviane Lamim, de Souza, Daiane Corrêa, Alvarenga, Tatiana Fonseca, Capela de Matos, Roberto R, Diniz, Claudia, Schramm, Marcia Trindade, Llerena Júnior, Juan Clinton, Silva, Maria Luiza Macedo, Abdelhay, Eliana, de Souza Fernandez, Teresa
Published in Molecular cytogenetics (11.07.2018)
Published in Molecular cytogenetics (11.07.2018)
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A unique set of complex chromosomal abnormalities in an infant with myeloid leukemia associated with Down syndrome
de Souza, Daiane Correa, de Figueiredo, Amanda Faria, Ney Garcia, Daniela R, da Costa, Elaine Sobral, Othman, Moneeb A K, Liehr, Thomas, Abdelhay, Eliana, Silva, Maria Luiza Macedo, de Souza Fernandez, Teresa
Published in Molecular cytogenetics (11.09.2017)
Published in Molecular cytogenetics (11.09.2017)
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A complex karyotype masked a cryptic variant t(8;21)(q22;q22) in a child with acute myeloid leukemia
Faria De Figueiredo, Amanda, Liehr, Thomas, Bhatt, Samarth, Binato, Renata, Tavares De Souza, Mariana, Rodrigues Capela De Matos, Roberto, De Jesus Marques Salles, Terezinha, Jordy, Fernanda C., Ribeiro, Raul C., Abdelhay, Eliana, Luiza Macedo Silva, Maria
Published in Leukemia & lymphoma (01.08.2011)
Published in Leukemia & lymphoma (01.08.2011)
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Molecular characterization of KMT2A fusion partner genes in 13 cases of pediatric leukemia with complex or cryptic karyotypes
Ney Garcia, Daniela R., Souza, Mariana T., Figueiredo, Amanda F., Othman, Moneeb A. K., Rittscher, Katharina, Abdelhay, Eliana, Capela de Matos, Roberto R., Meyer, Claus, Marschalek, Rolf, Land, Marcelo G. P., Liehr, Thomas, Ribeiro, Raul C., Silva, Maria Luiza Macedo
Published in Hematological oncology (01.12.2017)
Published in Hematological oncology (01.12.2017)
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Conventional and molecular cytogenetic characterization of Burkitt lymphoma with bone marrow involvement in Brazilian children and adolescents
De Souza, Mariana T., Hassan, Rocio, Liehr, Thomas, Marques-Salles, Terezinha J., Boulhosa, Alice M., Abdelhay, Eliana, Ribeiro, Raul C., Silva, Maria Luiza Macedo
Published in Pediatric blood & cancer (01.08.2014)
Published in Pediatric blood & cancer (01.08.2014)
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A case of childhood T cell acute lymphoblastic leukemia with a complex t(9;9) and homozygous deletion of CDKN2A gene associated with a Philadelphia-positive minor subclone
Ney-Garcia, Daniela Ribeiro, Vieira, Társis Paiva, Liehr, Thomas, Bhatt, Samarth, de Souza, Mariana Tavares, de Figueiredo, Amanda Faria, Ribeiro, Raul Correa, Silva, Maria Luiza Macedo
Published in Blood cells, molecules, & diseases (01.02.2013)
Published in Blood cells, molecules, & diseases (01.02.2013)
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A yet unreported der(11)t(6;11)(p21;q21) included in a complex karyotype of a refractory anemia with ring sideroblasts and poor prognosis
de Souza, Daiane Correa, de Figueiredo, Amanda Faria, Mkrtchyan, Hasmik, Othman, Moneeb A.K., Liehr, Thomas, Dobbin, Jane, Macedo Silva, Maria Luiza, Abdelhay, Eliana, de Souza Fernandez, Teresa
Published in Blood cells, molecules, & diseases (01.06.2014)
Published in Blood cells, molecules, & diseases (01.06.2014)
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A Novel Three-Way Variant t(8;13;21)(q22;q33;q22) in a Child with Acute Myeloid Leukemia with RUNX1/RUNX1T1 : The Contribution of Molecular Approaches for Revealing t(8;21) Variants
de Matos, Roberto R Capela, De Figueiredo, Amanda F, Liehr, Thomas, Alhourani, Eyad, De Souza, Mariana T, Binato, Renata, Ribeiro, Raul C, Silva, Maria Luiza Macedo
Published in Acta haematologica (01.01.2015)
Published in Acta haematologica (01.01.2015)
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A rare cryptic and complex rearrangement leading to MLL-MLLT10 gene fusion masked by del(10)(p12) in a child with acute monoblastic leukemia (AML-M5)
de Figueiredo, Amanda Faria, Vieira, Tarsis Paiva, Liehr, Thomas, Bhatt, Samarth, de Souza, Mariana Tavares, Binato, Renata, Marques-Salles, Terezinha de Jesus, Carboni, Edna, Ribeiro, Raul C, Silva, Maria Luiza Macedo, Abdelhay, Eliana
Published in Leukemia research (01.04.2012)
Published in Leukemia research (01.04.2012)
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Overexpression of the MLL Gene Combined With 11q Trisomy in a Child With Acute Lymphoblastic Leukemia
Ney Garcia, Daniela Ribeiro, de Figueiredo, Amanda Faria, Mencalha, André Luiz, de Matos, Roberto Rodrigues Capela, Neves, Fábia, Ribeiro, Raul Correa, Poirot Land, Marcelo Gerardin, Macedo Silva, Maria Luiza
Published in Clinical lymphoma, myeloma and leukemia (01.04.2014)
Published in Clinical lymphoma, myeloma and leukemia (01.04.2014)
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Molecular cytogenetic studies characterizing a novel complex karyotype with an uncommon 5q22 deletion in childhood acute myeloid leukemia
de Figueiredo, Amanda Faria, Capela de Matos, Roberto Rodrigues, Othman, Moneeb A K, Liehr, Thomas, da Costa, Elaine Sobral, Land, Marcelo Geradin Poirot, Ribeiro, Raul C, Abdelhay, Eliana, Silva, Maria Luiza Macedo
Published in Molecular cytogenetics (07.08.2015)
Published in Molecular cytogenetics (07.08.2015)
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Molecular cytogenetics reveals complex karyotype in apparent t(8;13) therapy-related acute myeloid leukemia M2 after fibrosarcoma
Soares-Ventura, Eliane Maria, Mkrtchyan, Hasmik, de Jesus Marques-Salles, Terezinha, Silva, Mariluze, Santos, Neide, de Araujo Silva Amaral, Bethania, Liehr, Thomas, Abdelhay, Eliana, Silva, Maria Luiza Macedo, Muniz, Maria Tereza Cartaxo
Published in Leukemia research (01.05.2011)
Published in Leukemia research (01.05.2011)
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A new cryptic ins(11;1)(q23;q21q31) detected in a t(1;8;11)(q21;p21;q23) in a baby with acute myeloid leukemia FAB AML-M5
de Figueiredo, Amanda Faria, Liehr, Thomas, Bath, Samarth, Binato, Renata, Ventura, Eliane Maria Soares, de Souza, Mariana Tavares, de Matos, Roberto Rodrigues Capela, Ribeiro, Raul Correa, Abdelhay, Eliana, Silva, Maria Luiza Macedo
Published in Blood cells, molecules, & diseases (15.10.2010)
Published in Blood cells, molecules, & diseases (15.10.2010)
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Unusual childhood biphenotypic acute leukemia with a yet unreported t(3;13)(p25.1;q13)
Marques-Salles, Terezinha de Jesus, Barros, Jemima Eline Xavier da Silva, Soares-Ventura, Eliane Maria, Cartaxo Muniz, Maria Tereza, Santos, Neide, Ferreira da Silva, Elizangela, Silva, Maria Luiza Macedo, Liehr, Thomas, Mkrtchyan, Hasmik
Published in Leukemia research (01.08.2010)
Published in Leukemia research (01.08.2010)
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Extra Copies of der(21)t(12;21) plus Deletion of ETV6 Gene due to dic(12;18) in B-Cell Precursor ALL with Poor Outcome
Liehr, Thomas, Santos, Neide, Silva, Maria Luiza Macedo, Hernandes, Marina Araújo Fonzar, Cornélio, Maria Teresa Marquim Nogueira, Muniz, Maria Tereza Cartaxo, Leite, Edinalva Pereira, Marques-Salles, Terezinha de Jesus, Mkrtchyan, Hasmik, Soares-Ventura, Eliane Maria
Published in Case reports in genetics (01.01.2012)
Published in Case reports in genetics (01.01.2012)
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New rearrangement t(3;17)(q26.3;q12) in an AML patient with a poor outcome
Macedo Silva, Maria Luiza, Land, Marcelo, Heller, Anita, Abdelhay, Eliana, do Socorro Pombo-de-Oliveira, Maria, Ribeiro, Raul, Alves, Gilda, Lerner, Décio, Liehr, Thomas
Published in Oncology reports (01.09.2005)
Published in Oncology reports (01.09.2005)
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Unbalanced chromosome 1 abnormalities leading to partial trisomy 1q in four infants with Down syndrome and acute megakaryocytic leukemia
Silva, Maria Luiza Macedo, Pombo-de-Oliveira, Maria do Socorro, Raimondi, Susana C, Mkrtchyan, Hasmik, Abdelhay, Eliana, de Figueiredo, Amanda Faria, de Souza, Mariana Tavares, Garcia, Daniela Ribeiro Ney, de Ventura, Eliane Maria Soares, de Sousa, Adriana Martins, Liehr, Thomas
Published in Molecular cytogenetics (19.02.2009)
Published in Molecular cytogenetics (19.02.2009)
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BCR - ABL1 co-occurring with CBFA2T3 - GLIS2 and RAM immunophenotype in a non-Down syndrome infant with acute megakaryoblastic leukemia
de Matos, Roberto R Capela, Ferreira, Gerson Moura, Bonecker, Simone, Rouxinol, Mainá, da Costa, Elaine Sobral, Mello, Fabiana V, Abdelhay, Eliana, Ribeiro, Raul C, Zalcberg, Ilana, Silva, Maria Luiza Macedo
Published in Leukemia & lymphoma (01.12.2023)
Published in Leukemia & lymphoma (01.12.2023)
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