Search Results - "Garcia, Daniela Ribeiro Ney"

Secondary abnormalities involving 1q or 13q and poor outcome in high stage Burkitt leukemia/lymphoma cases with 8q24 rearrangement at diagnosis by 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

“…Classical Burkitt lymphoma/leukemia (BL/L) presenting L3 morphology is found in 1% of childhood ALL. Recently, it has been described that secondary…”
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Overexpression of the MLL Gene Combined With 11q Trisomy in a Child With Acute Lymphoblastic Leukemia by 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

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Unbalanced chromosome 1 abnormalities leading to partial trisomy 1q in four infants with Down syndrome and acute megakaryocytic leukemia by 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

“…Children with Down syndrome (DS) have an increased risk of childhood acute leukemia, especially acute megakaryoblastic leukemia (AMKL) also called acute…”
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Intrachromosomal amplification of chromosome 21 (iAMP21) detected by ETV6/RUNX1 FISH screening in childhood acute lymphoblastic leukemia: a case report by Garcia, Daniela Ribeiro Ney, Arancibia, Alejandro Mauricio, Ribeiro, Raul C, Land, Marcelo Gerardin Poirot, Silva, Maria Luiza Macedo

“…Chromosome abnormalities that usually define high-risk acute lymphoblastic leukemia are the t(9;22)/ breakpoint cluster region protein-Abelson murine leukemia…”
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Molecular cytogenetic studies characterize a near-triploid complex karyotype in a child with acute lymphoblastic leukemia by Mkrtchyan, Hasmik, Garcia Ney, Daniela Ribeiro, de Ventura, Eliane Soares, Liehr, Thomas, Felix, Gabriel Rafael, de Jesus Marques-Salles, Terezinha, Abdelhay, Eliana, Macedo Silva, Maria Luiza

“…Abstract High hyperdiploidy with modal chromosome numbers between 50 and 65 is common in childhood acute lymphoblastic leukemia (ALL), occurring in 25–30% of…”
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Molecular studies reveal a MLL - MLLT3 gene fusion displaced in a case of childhood acute lymphoblastic leukemia with complex karyotype by Ney Garcia, Daniela Ribeiro, Liehr, Thomas, Emerenciano, Mariana, Meyer, Claus, Marschalek, Rolf, Pombo-de-Oliveira, Maria do Socorro, Ribeiro, Raul C, Poirot Land, Marcelo Gerardin, Macedo Silva, Maria Luiza

“…Rearrangement of the mixed lineage-leukemia gene ( MLL -r) is common in hematological diseases and is generally associated with poor prognosis. The…”
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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 by 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

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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 by 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

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