ANA
VILLEGAS MARTÍNEZ
Ikertzailea 2007-2012 tartean
Argitalpenak (134) ANA VILLEGAS MARTÍNEZ argitalpenak
2024
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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
2020
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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
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Hb Moncloa: A new variant of haemoglobin that interferes in the quantification of Hb A1c
Clinical Biochemistry, Vol. 50, Núm. 9, pp. 521-524
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Phenotype of mutations in the promoter region of the β-globin gene
Journal of Clinical Pathology, Vol. 70, Núm. 10, pp. 874-878
2016
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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
2015
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Asociación de la hemoglobina Groene Hart con la hemoglobina J-París-I: primer caso en España
Medicina Clinica, Vol. 144, Núm. 5, pp. 212-215
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Hb Cervantes, Hb Marañón, Hb La Mancha and Hb Goya: Description of 4 new haemoglobinopathies
Clinical Biochemistry, Vol. 48, Núm. 10-11, pp. 662-667
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Interobserver variance in myelodysplastic syndromes with less than 5 % bone marrow blasts: unilineage vs. multilineage dysplasia and reproducibility of the threshold of 2 % blasts
Annals of Hematology, Vol. 94, Núm. 4, pp. 565-573
2014
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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
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Hb Cibeles [α2 CD25(B6) (Gly → Asp)]: a novel alpha chain variant causing alpha-thalassemia
International Journal of Hematology, Vol. 100, Núm. 6, pp. 599-601
2013
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Association in cis of the mutations +20 (C>T) in the 5′ untranslated region and IVS-II-745 (C>G) on the β-globin gene
Hemoglobin, Vol. 37, Núm. 2, pp. 112-118
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Erythrocytosis in a child due to Hb andrew-minneapolis [β144(HC1) Lys→Asn (AAG>AAT or AAC)] associated with a Spanish (δβ) ;0-thalassemia
Hemoglobin, Vol. 37, Núm. 1, pp. 48-55
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Guidelines on haemovigilance of post-transfusional iron overload
Blood Transfusion, Vol. 11, Núm. 1, pp. 128-139
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Inter-observer variance with the diagnosis of myelodysplastic syndromes (MDS) following the 2008 WHO classification
Annals of Hematology, Vol. 92, Núm. 1, pp. 19-24
2012
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Another Hb with inclusion bodies β-thalassemia, owing to Hb Durham-N.C. [β114(G16) Leu > Pro]. First case described in Hispanic populations
Annals of Hematology
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Study of three families with Hb agrinio [α29(B10)Leu→Pro, CTG>CCG (α2)] in the spanish population: Three homozygous cases
Hemoglobin, Vol. 36, Núm. 6, pp. 526-532
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Thrombosis and severe asthenia as priority manifestations in paroxysmal nocturnal haemoglobinuria
Annals of Hematology
2011
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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
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Darbepoetin alfa for anemia in patients with low or intermediate-1 risk myelodysplastic syndromes and positive predictive factors of response
Current Medical Research and Opinion, Vol. 27, Núm. 5, pp. 951-960