¿Qué debe preguntar a su médico sobre la leucemia linfocítica aguda? Es importante sostener diálogos sinceros y honestos con su médico. Existen cuatro tipos principales de leucemia: Leucemia linfoblástica (linfocítica) aguda (ALL, por sus siglas en inglés). Leucemia mieloide (mielógena) aguda. Sin embargo, el aspecto cumbre de su estudio fue el descubrimiento, hace 30 años, de que la variedad más común en el niño, la leucemia linfocítica aguda.

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Chromosomal localization of human leukocyte, fibroblast, and immune interferon genes by means of in situ hybridization. This study focuses on the most important chromosomal abnormalities found in childhood ALL and their prognostic and therapeutic implications. Blood, 76pp. Blood, 87pp.

Preguntas que deben formularse acerca de la leucemia linfocítica aguda

Centric and pericentric chromosome rearrangements in hematopoietic malignancies. Unifirm approch to risk classification and treatment assignment to children with acute lymphoblastic leukemia.

N Engl J Med,pp. Blood, 8pp. Blood, 79pp.

Immunologic, cytogenetic, and clinical characterization of childhood acute lymphoblastic leukemia with the t 1;9 linfocitjca or its derivative. Localization the estrogen receptor locus ESR to chromosome 6q Nonrandom abnormalities of chromosome 9p in childhood acute lymphoblastic leukemia: Blood, 84pp.


Cancer, 40pp. Oncogene, 7pp. Identification of a gene, MLL, that spans the breakpoint in 11q23 translocations associated with human leukemias.

Factores de riesgo para la leucemia linfocítica aguda

Leukemia, 13pp. Br J Haematol, 90pp. The greatest impact on patient management has been the finding that the cytogenetic result is an independent prognostic indicator.

Genes Chromosom Cancer, 9pp.

Si continua navegando, consideramos que acepta su uso. Most patients with ALL show karyotype abnormalities, either in chromosome number ploidy or as structural changes such as translocations, inversions, or deletions. Hospital 12 de Octubre Edificio Materno-Infantil.

Blood, 65pp. Br J Haematol, 43pp.


Cytogenetic analysis of blast cells in childhood acute lymphoblastic leukemia has led to the recognition of specific non-random chromosomal abnormalities with prognostic value. Are you a health professional able to prescribe or dispense drugs? Blood, 77pp.

Genomics, 17pp. Prognostic implications of chromosomal findings in acute lymphoblastic leukemia at diagnosis. Nonrandom involvement of the 12p12 breakpoint in chromosome abnormalities of childhood acute lymphoblastic leukemia. Cytogenetic abnormalities in childhood acute lymphoblastic leukemia correlates with clinical features and treatmentoutcome.


This study focuses on the most important chromosomal abnormalities found in childhood ALL and their prognostic and therapeutic implications. To improve our services and products, we use “cookies” own or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior. Large-scale molecular mapping of human c-myb: Blood, 75pp.

Factores de riesgo para la leucemia linfocítica aguda

Sangre, 44pp. J Clin Oncol, 12pp. Leukemia, 7pp. You can change the settings or obtain more information by clicking here. Poor prognosis of children with pre-B acute lymphoblastic leukemia is associated with the t 1;19 q23,p Many of these chromosomal alterations are associated with specific cytomorphological and immunological types.

Collaborative lecuemia of karyotypes in childhood acute lymphoblastic leukemia.