Visualitza per autor "Mañu Pereira, M Mar"
Ara mostrant els elements 1-4 d 4
-
Combining microfluidics with machine learning algorithms for RBC classification in rare hereditary hemolytic anemia
Rizzuto, Valeria; Mencattini, Arianna; Álvarez‑González, Begoña; Di Giuseppe, Davide; Martinelli, Eugenio; Mañu Pereira, M Mar; Beneitez Pastor, David (Nature Research, 2021-06-30) -
Red Blood Cell Membrane Conductance in Hereditary Haemolytic Anaemias
Petkova-Kirova, Polina; Hertz, Laura; Danielczok, Jens; Huisjes, Rick; Makhro, Asya; Bogdanova, Anna; Mañu Pereira, M Mar (Frontiers Media, 2019-04-16) -
The use of next-generation sequencing in the diagnosis of rare inherited anaemias: A Joint BSH/EHA Good Practice Paper
Roy, Noemi; Da Costa, Lydie; Russo, Roberta; Bianchi, Paola; Mañu Pereira, M Mar; Fermo, Elisa (Wiley, 2022-08) -
Usefulness of NGS for Diagnosis of Dominant Beta-Thalassemia and Unstable Hemoglobinopathies in Five Clinical Cases
Rizzuto, Valeria; Koopmann, Tamara T.; Blanco Alvarez, Adoración; Tazón Vega, Bárbara; Idrizovic, Amira; Díaz de Heredia Rubio, Maria Cristina; Mañu Pereira, M Mar; Beneitez Pastor, David; Velasco Puyó, Pablo (Frontiers Media, 2021-02-05)