Publicaciones en las que colabora con EDUARDO LUIS ANGUITA MANDLY (24)

2011

  1. Caracterización molecular de dos nuevas mutaciones de α° talasemia en 2 familias españolas (mutación - ED y - GP)

    Medicina Clinica, Vol. 136, Núm. 15, pp. 674-677

2010

  1. GFI1B controls its own expression binding to multiple sites

    Haematologica, Vol. 95, Núm. 1, pp. 36-46

  2. Human promoter mutations unveil Oct-1 and GATA-1 opposite action on Gfi1b regulation

    Annals of Hematology, Vol. 89, Núm. 8, pp. 759-765

2009

  1. Haemoglobinopathies with high oxygen affinity. Experience of Erythropathology Cooperative Spanish Group

    Annals of Hematology, Vol. 88, Núm. 3, pp. 235-238

2001

  1. Monosomy for the most telomeric, gene-rich region of the short arm of human chromosome 16 causes minimal phenotypic effects

    European Journal of Human Genetics, Vol. 9, Núm. 3, pp. 217-225

  2. The thalassemia syndromes: Molecular characterization in the spanish population

    Hemoglobin, Vol. 25, Núm. 3, pp. 273-283

2000

  1. A new polymorphism (G→A) in the ψζ1 globin gene

    Haematologica, Vol. 85, Núm. 9, pp. 899-901

  2. Association of t(9;11)-MLL AF9 and trisomy 8 in an AML-M5 preceded by pancytopenia

    Cancer Genetics and Cytogenetics, Vol. 120, Núm. 2, pp. 144-147

  3. Hb Johnstown [β109 (G11) Val→Leu]: Second case described and associated for the first time with β0-thalassemia in two Spanish families

    American Journal of Hematology, Vol. 65, Núm. 4, pp. 298-301

  4. Homozygous Constant Spring: The first case described in the West

    Haematologica, Vol. 85, Núm. 6, pp. 667-669

  5. Is the α - (cal) mutation prevalent in central spain?

    Haematologica, Vol. 85, Núm. 1, pp. 100-101

1999

  1. Acute promyelocytic leukemia relapse in the central nervous system during hematologic and molecular remission [5]

    American Journal of Hematology

  2. Cleavage of the ALL1 gene in acute lymphoid leukemia before treatment disappears in relapse

    Haematologica, Vol. 84, Núm. 8, pp. 695-698

  3. Identification of the Hb Lepore phenotype by HPLC

    Haematologica, Vol. 84, Núm. 12, pp. 1081-1084

  4. Relación entre la persistencia del gen BCR/ABL y la recaída en pacientes adultos con leucemia linfoblástica aguda

    Medicina Clinica, Vol. 112, Núm. 13, pp. 481-484

1998

  1. Detection of bcr/abl mRNA in a case of chronic myelogenous leukemia in long-term remission: CML or sensitivity of detection?

    Haematologica, Vol. 83, Núm. 8, pp. 744-747

  2. High incidence of the CD8/9 (+G) β0-thalassemia mutation in Spain

    Haematologica, Vol. 83, Núm. 12, pp. 1066-1068

  3. Late relapse in BCR/ABL-positive patients after non-intensive chemotherapy [7]

    Leukemia

  4. The first report of a Philadelphia chromosome and BCR/ABL rearrangement positive myeloproliferative disorder in a child with thrombocythemia [2]

    Leukemia

  5. The importance of molecular screening of 11q23 abnormalities in childhood acute lymphoblastic leukemia: has the t(11;19)(q23;p13) a higher frequency than that revealed by conventional cytogenetic techniques?

    Medical and pediatric oncology