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Leucèmia i hemopaties pediàtriques

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Publicacions

  • Kozyra EJ, Pastor VB, Lefkopoulos S, Sahoo SS, Busch H, Voss RK, Erlacher M, Lebrecht D, Szvetnik EA, Hirabayashi S, Pasauliene R, Pedace L, Tartaglia M, Klemann C, Metzger P, Boerries M, Català-Temprano A, Hasle H, de Haas V, Kállay K, Masetti R, De Moerloose B, Dworzak M, Schmugge M, Smith O, Starý J, Mejstrikova E, Ussowicz M, Morris E, Singh P, Collin M, Derecka M, Göhring G, Flotho C, Strahm B, Locatelli F, Niemeyer CM, Trompouki E, Wlodarski MW and European Working Group of MDS in Childhood (EWOG-MDS).

    Synonymous GATA2 mutations result in selective loss of mutated RNA and are common in patients with GATA2 deficiency

    Leukemia . 34(10): 2673-2687. Nº de cites: 34

    [doi:10.1038/s41375-020-0899-5]

  • Montaño A, Hernández-Sánchez J, Forero-Castro M, Matorra-Miguel M, Lumbreras E, Miguel C, Santos S, Ramírez-Maldonado V, Fuster JL, de Las Heras N, García-de Coca A, Sierra M, Dávila J, de la Fuente I, Olivier C, Olazabal J, Martínez J, Vega-García N, González T, Hernández-Rivas JM and Benito R.

    Comprehensive Custom NGS Panel Validation for the Improvement of the Stratification of B-Acute Lymphoblastic Leukemia Patients

    Journal of Personalized Medicine . 10(3): 137. Nº de cites: 4

    [doi:10.3390/jpm10030137]

  • Fuster JL, Molinos-Quintana A, Fuentes C, Fernández JM, Velasco P, Pascual T, Rives-Solà S, Dapena JL, Sisinni L, López-Godino O, Palomo P, Villa-Alcázar M, Bautista F, González-Vicent M, López-Duarte M, García-Morín M, Ramos-Elbal E and Ramírez M.

    Blinatumomab and inotuzumab for B cell precursor acute lymphoblastic leukaemia in children: a retrospective study from the Leukemia Working Group of the Spanish Society of Pediatric Hematology and Oncology (SEHOP)

    BRITISH JOURNAL OF HAEMATOLOGY . 190(5): 764-771. Nº de cites: 20

    [doi:10.1111/bjh.16647]

  • Bardón Cancho EJ, García-Morín M, Beléndez C, Velasco P, Benéitez D, Ruiz-Llobet A, Berrueco R, Argilés B, Cervera Á, Salinas JA, Vecilla C, Gondra A, Vallés G, Murciano T, Bermúdez M and Cela E.

    Update of the Spanish registry of haemoglobinopathies in children and adults

    MEDICINA CLINICA . 155(3): 95-103. Nº de cites: 15

    [doi:10.1016/j.medcli.2019.10.011]

  • Rey-Barroso L, Roldan-Molina M, Burgos-Fernández FJ, Gassiot S, Ruiz-Llobet A, Isola I and Vilaseca MA.

    Spectroscopic Evaluation of Red Blood Cells of Thalassemia Patients with Confocal Microscopy: A Pilot Study

    SENSORS . 20(14): . Nº de cites: 6

    [doi:10.3390/s20144039]

  • Molina O, Vinyoles M, Granada I, Roca-Ho H, Gutierrez-Agüera F, Valledor L, López-López CM, Rodríguez-González P, Trincado JL, Tirados-Menéndez S, Pal D, Ballerini P, Den Boer ML, Plensa-Nebot I, Pérez-Iribarne MM, Rodriguez-Perales S, Calasanz MJ, Ramírez M, Rodríguez R, Camós-Guijosa M, Calvo M, Bueno C and Menendez P.

    Impaired condensin complex and Aurora B kinase underlie mitotic and chromosomal defects in hyperdiploid B-cell ALL

    Blood . 136(3): 313-327. Nº de cites: 19

    [doi:10.1182/blood.2019002538]

  • Mirones I, Moreno L, Patiño-García A, Lizeaga G, Moraleda JM, Toribio ML and Pérez-Martínez A.

    Inmunoterapia con células CAR-T en hematooncología pediátrica.

    ANALES DE PEDIATRIA . 93(1): . Nº de cites: 1

    [doi:10.1016/j.anpedi.2019.12.014]

  • Català-Temprano A, Ali SS, Cuvelier GDE, Steele M, Klaassen RJ, Fernandez CV, Pastore YD, Abish S, Rayar M, Jardine L, Breakey VR, Brossard J, Sinha R, Silva M, Goodyear L, Lipton JH, Michon B, Corriveau-Bourque C, Sung L, Lauhasurayotin S, Zlateska B, Cada M and Dror Y.

    Androgen therapy in inherited bone marrow failure syndromes: analysis from the Canadian Inherited Marrow Failure Registry.

    BRITISH JOURNAL OF HAEMATOLOGY . 189(5): 976-981. Nº de cites: 8

    [doi:10.1111/bjh.16445]

  • Hrusak O, Kalina T, Wolf J, Balduzzi A, Provenzi M, Rizzari C, Rives-Solà S, Del Pozo Carlavilla M, Alonso MEV, Domínguez-Pinilla N, Bourquin JP, Schmiegelow K, Attarbaschi A, Grillner P, Mellgren K, van der Werff Ten Bosch J, Pieters R, Brozou T, Borkhardt A, Escherich G, Lauten M, Stanulla M, Smith O, Yeoh AEJ, Elitzur S, Vora A, Li CK, Ariffin H, Kolenova A, Dallapozza L, Farah R, Lazic J, Manabe A, Styczynski J, Kovacs G, Ottoffy G, Felice MS, Buldini B, Conter V, Stary J and Schrappe M.

    Flash survey on severe acute respiratory syndrome coronavirus-2 infections in paediatric patients on anticancer treatment

    EUROPEAN JOURNAL OF CANCER . 132: 11-16. Nº de cites: 130

    [doi:10.1016/j.ejca.2020.03.021]

  • Bogliolo M, Pujol R, Aza-Carmona M, Muñoz-Subirana N, Rodriguez-Santiago B, Casado JA, Rio P, Bauser C, Reina-Castillón J, Lopez-Sanchez M, Gonzalez-Quereda L, Gallano P, Català-Temprano A, Ruiz-Llobet A, Badell I, Diaz-Heredia C, Hladun R, Senent L, Argiles B, Bergua Burgues JM, Bañez F, Arrizabalaga B, López Almaraz R, Lopez M, Figuera Á, Molinés A, Pérez de Soto I, Hernando I, Muñoz JA, Del Rosario Marin M, Balmaña J, Stjepanovic N, Carrasco E, Cuesta I, Cosuelo JM, Regueiro A, Moraleda Jimenez J, Galera-Miñarro AM, Rosiñol L, Carrió A, Beléndez-Bieler C, Escudero Soto A, Cela E, de la Mata G, Fernández-Delgado R, Garcia-Pardos MC, Sáez-Villaverde R, Barragaño M, Portugal R, Lendinez F, Hernadez I, Vagace JM, Tapia M, Nieto J, Garcia M, Gonzalez M, Vicho C, Galvez E, Valiente A, Antelo ML, Ancliff P, Garcia F, Dopazo J, Sevilla J, Paprotka T, Pérez-Jurado LA, Bueren J and Surralles J.

    Optimised molecular genetic diagnostics of Fanconi anaemia by whole exome sequencing and functional studies

    JOURNAL OF MEDICAL GENETICS . 57(4): 258-268. Nº de cites: 20

    [doi:10.1136/jmedgenet-2019-106249]