Investigación

Leucemia y hemopatías pediátricas

Buscador de publicaciones

Publicaciones

  • Parisi C, Candela-Cantó SA, Serrano M, Català-Temprano A, Aparicio J and Hinojosa J.

    Life-threatening secondary hemophagocytic lymphohistiocytosis following vagal nerve stimulator infection in a child with CHD2 myoclonic encephalopathy: a case report

    CHILDS NERVOUS SYSTEM . 36(11): 2851-2856. Nº de citas: 3

    [doi:10.1007/s00381-020-04558-x]

  • Salvador, PP, Benjamin, RS, Manel, BG, Angel, FRS, Montserrat, TE, Badell-Serra I, Jordi, SC and Jorge, SG.

    APPLICATION OF THE CLINICAL EXOMA "SANT PAU" FOR THE DIAGNOSIS OF HEMOLITIC ANEMIAS AND HEREDITARY IRON METABOLISM DISORDERS

    HAEMATOLOGICA . 105: 33-33.

    [doi:10.3324/haematol.2020.s3]

  • 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 citas: 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 citas: 7

    [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 citas: 21

    [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 citas: 16

    [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 citas: 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 citas: 20

    [doi:10.1182/blood.2019002538]

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

    Immunotherapy with CAR-T cells in paediatric haematology-oncology

    ANALES DE PEDIATRIA . 93(1): . Nº de citas: 2

    [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 citas: 9

    [doi:10.1111/bjh.16445]