Zobrazeno 1 - 10
of 393
pro vyhledávání: '"E, Abdelhay"'
Autor:
RRC Matos, GM Ferreira, AF Figueiredo, E Abdelhay, TJ Marques-Salles, L Otero, EF Rocha, MGP Land, I Zalcberg, MLM Silva
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 45, Iss , Pp S586-S587 (2023)
Objectives: Leukemia is the most common childhood malignancy, with an incidence of 4.7 per 100,000 in pediatric patients (< 20 years of age). Acute Leukemias (AL) represent a heterogeneous group of diseases that originate from the interaction between
Externí odkaz:
https://doaj.org/article/4e602bf456414775aa48bcbbf276b480
Autor:
RRC Matos, KC Monteso, MT Bizarro, MM Rocha, T Liehr, M Rouxinol, E Abdelhay, R Binato, RC Ribeiro
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss , Pp S279-S280 (2021)
Objectives: Core binding factor (CBF) leukemias represent an important prognostic group in acute myeloid leukemia (AML). The t(8;21)(q22;q22)/RUNX1 -RUNX1T1 is one of the most frequent abnormalities in childhood AML (7–16%) and is related to a good
Externí odkaz:
https://doaj.org/article/b6f646e0a6dc4205b649cc44a7b16fc1
Autor:
RRC Matos, GM Ferreira, KC Monteso, MT Bizarro, M Othman, T Liehr, M Rouxinol, E Abdelhay, R Binato, MLM Silva
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss , Pp S295-S296 (2021)
Objectives: Intrachromosomal amplification of chromosome 21 (iAMP21) occurs in 2% of B-cell acute lymphoblastic leukemia (ALL) and is considered to confer a poor prognosis. Alterations related to chromosome 21, such as the constitutional r(21)c and r
Externí odkaz:
https://doaj.org/article/85fd8e6e1a234ade9a1eb2589b4204cb
Autor:
GM Ferreira, RRC Matos, KC Monteso, MM Rocha, MT Bizarro, C Meyer, T Liehr, E Abdelhay, R Binato, MLM Silva
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss , Pp S300- (2021)
Objectives: KMT2A gene aberrations are more frequent in infants less than one year (yr) of age, accounting for about 70% of acute lymphoblastic leukemia (ALL) patients, and about 30% are diagnosed with acute myeloid leukemia (AML). The most common ab
Externí odkaz:
https://doaj.org/article/f4ce8fb1bfe94a3385d4ef477181226e
Autor:
VL Lovatel, EF Rodrigues, CS Fernandez, RC Tavares, APS Bueno, AS Fonte, ES Costa, E Abdelhay, SCS Lima, TS Fernandez
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss , Pp S303-S304 (2021)
Objetivos: A síndrome mielodisplásica pediátrica (SMD-p) é rara, sua etiopatologia é complexa e ainda não se sabe a causa de seu surgimento. Embora avanços rápidos tenham sido feitos na SMD no adulto, a genética e epigenética da SMD-p ainda
Externí odkaz:
https://doaj.org/article/85b587a793e94267adbd33f407d53c7e
Autor:
G.E.B. Oliveira, S.T. Oliveira, M.E.F. Vasselai, F.M.A.J.F. Silva, M.R. Garbim, S. Corrêa, F.C. Trigo, E. Abdelhay, C. Panis
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 42, Iss , Pp 305-306 (2020)
Externí odkaz:
https://doaj.org/article/6709c3c5c9d549edb5516611168275ca
Autor:
R R, Capela de Matos, Mak, Othman, G M, Ferreira, Kca, Monteso, M T, de Souza, M, Rouxinol, J B, Melo, I M, Carreira, E, Abdelhay, T, Liehr, R C, Ribeiro, Mlm, Silva
Publikováno v:
Cancer Genetics. :16-22
Intrachromosomal amplification of chromosome 21 (iAMP21) occurs in ∼2% of B-cell acute lymphoblastic leukemia (ALL) and is considered to confer a poor prognosis. The relapse risk is associated with therapy intensity, suggesting that other somatic m
Akademický článek
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Akademický článek
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Publikováno v:
ESMO Open. 8:101474