Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Hematological Oncology|August 16, 2021
Lower incidence of clinical allergy with PEG-asparaginase upfront versus the sequential use of native E. coli asparaginase followed by PEG-ASP in pediatric patients with acute lymphoblastic leukemiaMontserrat Mesegué, Anna Alonso-Saladrigues, Sara Pérez-Jaume, et al.
British Journal of Haematology|July 7, 2018
Paediatric patients with acute leukaemia and KMT2A (MLL) rearrangement show a distinctive expression pattern of histone deacetylasesNerea Vega-García, Roberta Malatesta, Camino Estella, et al.
Medicina Clinica|March 2, 2020
Update of the Spanish registry of haemoglobinopathies in children and adultsEduardo J Bardón Cancho, Marina García-Morín, Cristina Beléndez, et al.
JCI Insight|May 22, 2024
Lentivirus-mediated gene therapy corrects ribosomal biogenesis and shows promise for Diamond Blackfan anemiaYari Giménez, Manuel Palacios, Rebeca Sánchez-Domínguez, et al.
Annals of Hematology|March 23, 2024
Spanish registry of hemoglobinopathies and rare anemias (REHem-AR): demographics, complications, and management of patients with β-thalassemiaEduardo J Bardón-Cancho, José Manuel Marco-Sánchez, David Benéitez-Pastor, et al.
Journal of Thrombosis and Haemostasis : JTH|March 15, 2022
Venous thromboembolism in pediatric patients with acute lymphoblastic leukemia under chemotherapy treatment. Risk factors and usefulness of thromboprophylaxis. Results of LAL-SEHOP-PETHEMA-2013Anna Ruiz-Llobet, Susanna Gassiot, Edurne Sarrate, et al.
Orphanet Journal of Rare Diseases|April 19, 2019
Genetic analyses of aplastic anemia and idiopathic pulmonary fibrosis patients with short telomeres, possible implication of DNA-repair genesElena G Arias-Salgado, Eva Galvez, Lurdes Planas-Cerezales, et al.
Annals of Hematology|May 19, 2024
Haemoglobinopathies and other rare anemias in Spain: ten years of a nationwide registry (REHem-AR)José Manuel Marco Sánchez, Eduardo Jesús Bardón Cancho, David Benéitez, et al.
International Journal of Neonatal Screening|October 25, 2024
Newborn Screening for Sickle Cell Disease in Catalonia between 2015 and 2022-Epidemiology and Impact on Clinical EventsJosé Manuel González de Aledo-Castillo, Ana Argudo-Ramírez, David Beneitez-Pastor, et al.
Orphanet Journal of Rare Diseases|April 16, 2025
COVID- 19 in patients affected by red blood cell disorders, results from the European registry ERN-EuroBloodNetPablo Velasco Puyo, Soteroula Christou, Saveria Campisi, et al.
Pageof 2