Missense variants in ALAS2 gene in five patients by Moreno‐Carralero, María‐Isabel, Arrizabalaga‐Amuchastegui, Beatriz, Sánchez‐Calero‐Guilarte, Jorge, Morado‐Arias, Marta, Velasco‐Valdazo, Alberto‐Eterio, de‐la‐Iglesia‐Iñigo, Silvia, Méndez, Manuel, Morán‐Jiménez, María‐José

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Early‐onset reduced bone mineral density in patients with pyruvate kinase deficiency by Al‐Samkari, Hanny, Grace, Rachael F., Glenthøj, Andreas, Andres, Oliver, Barcellini, Wilma, Galactéros, Frédéric, Kuo, Kevin H. M., Layton, D. Mark, Morado Arias, Marta, Viprakasit, Vip, Dong, Yan, Tai, Feng, Hawkins, Peter, Gheuens, Sarah, Morales‐Arias, Jaime, Gilroy, Keely S., Porter, John B., Beers, Eduard J.

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Sideroblastic anemia: functional study of two novel missense mutations in ALAS2 by Méndez, Manuel, Moreno‐Carralero, María‐Isabel, Morado‐Arias, Marta, Fernández‐Jiménez, María‐Cristina, Iglesia Iñigo, Silvia, Morán‐Jiménez, María‐José

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Sideroblastic anemia: functional study of two novel missense mutations in ALAS 2 by Méndez, Manuel, Moreno‐Carralero, María‐Isabel, Morado‐Arias, Marta, Fernández‐Jiménez, María‐Cristina, de la Iglesia Iñigo, Silvia, Morán‐Jiménez, María‐José

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Response to Pegcetacoplan in Patients with PNH Assessed By Erythroid Clonal Size and Laboratory Markers by Morado-Arias, Marta, Ballesteros, Monica, Gómez-Álvarez, Miguel, Herrera, Federico, Villegas, Ana

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uRADAR: European Patients Referral Frame to Improve Access to New Drugs and Therapies in Ultra-Rare Anemia Disorders and Severe Hereditary Spherocytosis by Rodríguez Sánchez, Maria A., Collado Gimbert, Anna, Reidel, Sara, Aguilar-Martinez, Patricia, Bento, Celeste, Cela, Elena, Dedeken, Laurence, Drasar, Emma, Galacteros, Frederic, Glenthoej, Andreas, Horvathova, Monika, Koralkova, Pavla, Kulozik, Andreas E., Kunz, Joachim B., Morado-Arias, Marta, Ortuno Cabrero, Ana, Pospíšilová, Dagmar, Rab, Minke A.E., Roy, Noemi, Van Beers, Eduard J., van Wijk, Richard, Wambacq, Sarah, Diot, Claire, Gutiérrez Valle, Victoria, Mosull del Campo, Raquel, Tamana, Stella, Colombatti, Raffaella, Kountouris, Petros, Gulbis, Béatrice, Bianchi, Paola, Mañú-Pereira, Maria del Mar

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Molecular Characterization of Hemoglobin H Disease in Spain by Ropero Gradilla, Paloma, Villegas, Ana, Menor Gómez, María, Ferrer, Sara, Lopez-Duarte, Monica, Muruzábal Sitges, María José, Arbeteta Juanis, Jaime, Ibañez Royo, María Dolores, Recasens Flores, Valle, Montañés García, María Ángeles, Ordoñez García, María, Solano Ramos, Fernando, Lerma Verdejo, Ana, Martín Gulino, Horacio, Abío Calvete, Mariola, López Rubio, Montserrat, Ricard Andrés, Pilar, Morado Arias, Marta, Ortega Montero, Belén, Tenorio Núñez, María, Salido, Eduardo José, Lo Riso, Laura, Vara, Míriam, Zamanilllo Herreros, Irene, Guerrero Fernández, Lucía, Senent Peris, María Leonor, Fernandez Garcia, Sergio, Martínez Nieto, Jorge, Gómez Álvarez, Miguel, Fernandez, Fernando Ataulfo Gonzalez, Benavente Cuesta, Celina, Sehh, Grupo Español de Eritropatología

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Clinical and genetic features of congenital dyserythropoietic anemia (CDA) by Moreno‐Carralero, María‐Isabel, Horta‐Herrera, Saul, Morado‐Arias, Marta, Ricard‐Andrés, María‐Pilar, Lemes‐Castellano, Angelina, Abio‐Calvete, Mariola, Cedena‐Romero, María‐Teresa, González‐Fernández, Fernando‐Ataulfo, Llorente‐González, Laura, Periago‐Peralta, Adela‐María, de‐la‐Iglesia‐Íñigo, Silvia, Méndez, Manuel, Morán‐Jiménez, María‐José

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Missense variants in ALAS 2 gene in five patients by Moreno‐Carralero, María‐Isabel, Arrizabalaga‐Amuchastegui, Beatriz, Sánchez‐Calero‐Guilarte, Jorge, Morado‐Arias, Marta, Velasco‐Valdazo, Alberto‐Eterio, de‐la‐Iglesia‐Iñigo, Silvia, Méndez, Manuel, Morán‐Jiménez, María‐José

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Autoimmune haemolytic anaemias: A retrospective study of 93 patients by Gutiérrez Jomarrón, Isabel, López Rubio, Montserrat, Morado Arias, Marta, Arrizabalaga, Beatriz, de la Iglesia, Silvia, Beneitez, David, Sáez, María Isabel, Cervera, Aurea, Recasens, Valle, Herrera, Ascensión, Villegas, Ana María

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