Hereditary elliptocytosis: A novel mutation in the SPTA1 gene and diagnosis after a stroke in paediatric patients. A two‐case report von Moreno Toro, Noelia, Gámez Belmonte, Ana, Alperi García, Sofía, Morillas Mingorance, Ángel, Ortega Acosta, María José, Urrutia Maldonado, Emilia, Bernal Sánchez, Mónica, Peláez Pleguezuelos, Irene

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Venous thromboembolism in pediatric patients with acute lymphoblastic leukemia under chemotherapy treatment. Risk factors and usefulness of thromboprophylaxis. Results of LAL‐SEHOP... von Ruiz‐Llobet, Anna, Gassiot, Susanna, Sarrate, Edurne, Zubicaray, Josune, Dapena, José Luis, Rives, Susana, Sevilla, Julián, Menárguez López, Ángela, Panesso Romero, Melissa, Montoya, Catalina, Vagace, José Manuel, Molina Hurtado, José Ramón, García‐Morín, Marina, García Abós, Miriam, Mendoza Sánchez, María Carmen, Lendínez, Francisco, Palomo Moraleda, Pilar, Tallón, María, González, Berta, Urrutia, Emilia, Serna, José Vicente, Peláez Pleguezuelos, Irene, Martínez Merino, Marta, Ramos Elbal, Eduardo, Orellana, Elena, Benítez Muñoz, Helga, Berrueco, Rubén

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Spanish registry of hemoglobinopathies and rare anemias (REHem-AR): demographics, complications, and management of patients with β-thalassemia von Bardón-Cancho, Eduardo J., Marco-Sánchez, José Manuel, Benéitez-Pastor, David, Payán-Pernía, Salvador, Llobet, Anna Ruiz, Berrueco, Rubén, García-Morin, Marina, Beléndez, Cristina, Senent, Leonor, Acosta, María José Ortega, Pleguezuelos, Irene Peláez, Velasco, Pablo, Collado, Anna, Moreno-Carbonell, Marta, Argilés, Bienvenida, de Soto, Inmaculada Pérez, del Mar Bermúdez, María, Salido Fiérrez, Eduardo J., Blanco-Álvarez, Adoración, Navarro, Pablo González, Cela, Elena

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Abstract 9749: Anthracicline-Induced Cardiotoxicity in Children. Pharmacogenetics and Clinical Study at a Tertiary Center von Moreno Toro, Noelia, Marangoni Iglecias, Luciana María, CARRERAS BLESA, CARMEN, Rodriguez Vazquez del Rey, Maria del Mar, Urrutia Maldonado, Emilia, ortega Acosta, maria jose, Pascual Gázquez, Juan Francisco, Pelaez Pleguezuelos, Irene, Perin, Francesca

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Inherited Thrombocytopenias Predisposing to Hematologic Neoplasms. Experience of the Spanish Group for Inherited Platelet Disorders (GEAPC) von Bastida, Jose Maria, Marín-Quílez, Ana, Zamora, Ana, Benito Sanchez, Maria Rocio, Rodriguez Alen, Agustín, Sevivas, Teresa, Gómez-González, Pedro Luis, Díaz-Ajenjo, Lorena, Butta, Nora, Campos, Rosa M., Escribano, Paola, Huertas-Aragoneses, Jorge, Lopez-Duarte, Monica, León, Antonio, Mompel, Angela, De Oña Navarrete, Raquel, Peláez-Pleguezuelos, Irene, Ramos-Ortega, Fernando Jesús, Sebastian, Elena, Serrano, Claudia, Sierra-Aisa, Cristina, Velasco, Pablo, Murillo, Laura, Vidal-Laso, Rosa, Nomdedeu, Meritxell, Esteve Reyner, Jordi, Hernández-Rivas, Jesús María, Rivera Pozo, Jose, Lozano, Maria Luisa

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Correction to: Spanish registry of hemoglobinopathies and rare anemias (REHem- AR): demographics, complications, and management of patients with β-thalassemia von Bardón-Cancho, Eduardo J., Marco-Sánchez, José Manuel, Benéitez-Pastor, David, Payán-Pernía, Salvador, Llobet, Anna Ruiz, Berrueco, Rubén, García-Morin, Marina, Beléndez, Cristina, Senent, Leonor, Acosta, María José Ortega, Pleguezuelos, Irene Peláez, Velasco, Pablo, Collado, Anna, Moreno-Carbonell, Marta, Argilés, Bienvenida, de Soto, Inmaculada Pérez, del Mar Bermúdez, María, Salido Fiérrez, Eduardo J., Blanco-Álvarez, Adoración, Navarro, Pablo González, Cela, Elena

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Spanish registry of hemoglobinopathies and rare anemias (REHem-AR) : demographics, complications, and management of patients with β-thalassemia von Bardón-Cancho, Eduardo J, Marco-Sánchez, José Manuel, Beneitez Pastor, David, Payán-Pernía, Salvador, Llobet, Anna Ruiz, Berrueco, Rubén, García-Morin, Marina, Beléndez, Cristina, Senent, Leonor, Ortega Acosta, María José, Peláez Pleguezuelos, Irene, Velasco, Pablo, Collado, Anna, Moreno-Servet, Marta, Argilés, Bienvenida, Pérez de Soto, Inmaculada, Bermúdez, María del Mar, Salido Fiérrez, Eduardo J, Blanco, Adoración, González Navarro, Pablo, Cela, Elena, Universitat Autònoma de Barcelona

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Hereditary elliptocytosis: A novel mutation in the SPTA1 gene and diagnosis after a stroke in paediatric patients. A two-case report von Moreno Toro, Noelia, Gámez Belmonte, Ana, Alperi García, Sofía, Morillas Mingorance, Ángel, Ortega Acosta, María José, Urrutia Maldonado, Emilia, Bernal Sánchez, Mónica, Peláez Pleguezuelos, Irene

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