Publicaciones en las que colabora con ANA VILLEGAS MARTÍNEZ (13)

2024

  1. Largest comparison between onset and relapses of acquired thrombotic thrombocytopenic purpura reveals severe neurological involvement and worse analytic parameters at debut

    Annals of Hematology, Vol. 103, Núm. 3, pp. 725-727

2023

  1. Mutations in the RACGAP1 gene cause autosomal recessive congenital dyserythropoietic anemia type III

    Haematologica

2020

  1. Diagnóstico diferencial de las eritrocitosis. Hemoglobinas con alta afinidad por el oxígeno

    Anales de la Real Academia Nacional de Medicina, Núm. 137, pp. 35-43

2017

  1. Hb Moncloa: A new variant of haemoglobin that interferes in the quantification of Hb A1c

    Clinical Biochemistry, Vol. 50, Núm. 9, pp. 521-524

  2. Phenotype of mutations in the promoter region of the β-globin gene

    Journal of Clinical Pathology, Vol. 70, Núm. 10, pp. 874-878

2016

  1. HB Puerta del Sol [HBA1:c.148A>C], HB Valdecilla [HBA2:c.3G>T], HB Gran Vía [HBA2:c.98T>G], HB Macarena [HBA2:c.358C>T] and HB El Retiro [HBA2:c.364-366dupGTG]: Description of five new hemoglobinopathies

    Clinical Chemistry and Laboratory Medicine, Vol. 54, Núm. 4, pp. 553-560

2014

  1. A novel antibody against human factor B that blocks formation of the C3bB proconvertase and inhibits complement activation in disease models

    Journal of Immunology, Vol. 193, Núm. 11, pp. 5567-5575

2011

  1. Hemoglobin Seville [α2 β2 81(EF5) Leu → Phe] a silent phenotypic variant that interferes in hemoglobin A1c measurement by ion-exchange HPLC method

    Clinical Biochemistry, Vol. 44, Núm. 10-11, pp. 933-935

2009

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

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

2005

  1. A deletion of 11 bp (CD 131-134) in exon 3 of the β-globin gene produces the phenotype of inclusion body β-thalassemia

    Annals of Hematology, Vol. 84, Núm. 9, pp. 584-587

  2. Distribución geográfica de las mutaciones del gen HFE en España

    Medicina Clinica

2004

  1. Receptor sérico de transferrina en niños sanos. Valor diagnóstico en la anemia infecciosa y en la ferropénica

    Anales de Pediatria, Vol. 60, Núm. 5, pp. 428-435

1994

  1. Acquired hemoglobin H disease associated with a myelodysplastic syndrome

    Sangre, Vol. 39, Núm. 3, pp. 211-213