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Rabbit antithymocyte globulin versus horse antithymocyte globulin for treatment of acquired aplastic anemia: a retrospective analysis.
Vallejo C, Montesinos P, Polo M, Cuevas B, Morado M, Rosell A, Xicoy B, Díez JL, Salamero O, Cedillo Á, Martínez P, Rayón C; Bone Marrow Failure Spanish Study Group (Pethema-GETH). Vallejo C, et al. Among authors: morado m. Ann Hematol. 2015 Jun;94(6):947-54. doi: 10.1007/s00277-015-2305-3. Epub 2015 Feb 13. Ann Hematol. 2015. PMID: 25672649
Diagnostic screening of paroxysmal nocturnal hemoglobinuria: Prospective multicentric evaluation of the current medical indications.
Morado M, Freire Sandes A, Colado E, Subirá D, Isusi P, Soledad Noya M, Belén Vidriales M, Sempere A, Ángel Díaz J, Minguela A, Álvarez B, Serrano C, Caballero T, Rey M, Pérez Corral A, Cristina Fernández Jiménez M, Magro E, Lemes A, Benavente C, Bañas H, Merino J, Castejon C, Gutierrez O, Rabasa P, Vescosi Gonçalves M, Perez-Andres M, Orfao A; PNH working group of the Iberian Society of Cytometry (SIC). Morado M, et al. Cytometry B Clin Cytom. 2017 Sep;92(5):361-370. doi: 10.1002/cyto.b.21480. Epub 2016 Oct 1. Cytometry B Clin Cytom. 2017. PMID: 27598686 Free article.
Consensus document for the diagnosis and treatment of pyruvate kinase deficiency.
Morado M, Villegas AM, de la Iglesia S, Martínez-Nieto J, Del Orbe Barreto R, Beneitez D, Salido E; en representación del Grupo Español de Eritropatología. Morado M, et al. Med Clin (Barc). 2021 Sep 10;157(5):253.e1-253.e8. doi: 10.1016/j.medcli.2020.10.018. Epub 2021 Jan 9. Med Clin (Barc). 2021. PMID: 33431182 English, Spanish.
[Paroxysmal nocturnal hemoglobinuria therapy with eculizumab: Spanish experience].
López Rubio M, Morado M, Gaya A, Alonso Rosa D, Ojeda E, Muñoz JA, Pérez de Mendiguren B, Monteagudo MD, Durán JM, Fisac RM, Moreno D, Villegas AM. López Rubio M, et al. Among authors: morado m. Med Clin (Barc). 2011 Jun 11;137(1):8-13. doi: 10.1016/j.medcli.2010.09.035. Epub 2011 Feb 5. Med Clin (Barc). 2011. PMID: 21296371 Spanish.
Mutations in the RACGAP1 gene cause autosomal recessive congenital dyserythropoietic anemia type III.
Hernández G, Romero-Cortadellas L, Ferrer-Cortès X, Venturi V, Dessy-Rodriguez M, Olivella M, Husami A, De Soto CP, Morales-Camacho RM, Villegas A, González-Fernández FA, Morado M, Kalfa TA, Quintana-Bustamante O, Pérez-Montero S, Tornador C, Segovia JC, Sánchez M. Hernández G, et al. Among authors: morado m. Haematologica. 2023 Feb 1;108(2):581-587. doi: 10.3324/haematol.2022.281277. Haematologica. 2023. PMID: 36200420 Free PMC article. No abstract available.
44 results