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Publicacions

  • 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: 17

    [doi:10.1136/jmedgenet-2019-106249]

  • Santoro C, Fuh B, Le PQ, Maes P, Berrueco R, Mingot-Castellano EM, von Mackensen S, Solms A and Wang M.

    BAY 81-8973 prophylaxis and pharmacokinetics in haemophilia A: Interim results from the TAURUS study

    EUROPEAN JOURNAL OF HAEMATOLOGY . 105(2): 164-172. Nº de cites: 3

    [doi:10.1111/ejh.13420]

  • Castella M, Caballero-Baños M, Ortiz-Maldonado V, González-Navarro EA, Suñé G, Antoñana-Vidósola A, Boronat A, Marzal B, Millán L, Martín-Antonio B, Jordi Cid Colom, Lozano M, García E, Tabera J, Trias E, Perpiña U, Canals JM, Baumann T, Benítez-Ribas D, ELENA CAMPO, Yagüe-Ribes J, Urbano-Ispizua Á, Rives-Solà S, Delgado J and Juan-Otero M.

    Point-Of-Care CAR T-Cell Production (ARI-0001) Using a Closed Semi-automatic Bioreactor: Experience From an Academic Phase I Clinical Trial

    FRONTIERS IN IMMUNOLOGY . 11: 482-482. Nº de cites: 73

    [doi:10.3389/fimmu.2020.00482]

  • Ruiz-Llobet A, Isola I, Gassiot S, Català-Temprano A, Díaz-Ricart M, Martinez-Monseny T, Serrano M and Berrueco R.

    Platelet Dysfunction in Noonan and 22q11.2 Deletion Syndromes in Childhood

    THROMBOSIS AND HAEMOSTASIS . 120(3): 457-465. Nº de cites: 3

    [doi:10.1055/s-0040-1701239]

  • 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 cites: 2

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

  • Borràs N, Garcia-Martínez I, Batlle J, Pérez-Rodríguez A, Parra R, Altisent C, López-Fernández MF, Costa Pinto J, Batlle-López F, Cid AR, Bonanad S, Cabrera N, Moret A, Mingot-Castellano ME, Navarro N, Pérez-Montes R, Marcellini S, Moreto A, Herrero S, Soto I, Fernández-Mosteirín N, Jiménez-Yuste V, Alonso N, de Andrés-Jacob A, Fontanes E, Campos R, Paloma MJ, Bermejo N, Berrueco R, Mateo J, Arribalzaga K, Marco P, Palomo Á, Castro Quismondo N, Iñigo B, Del Mar Nieto M, Vidal R, Martínez MP, Aguinaco R, Tenorio M, Ferreiro M, García-Frade J, Rodríguez-Huerta AM, Cuesta J, Rodríguez-González R, García-Candel F, Dobón M, Aguilar C, Corrales I and Vidal F.

    Unraveling the Influence of Common von Willebrand factor variants on von Willebrand Disease Phenotype: An Exploratory Study on the Molecular and Clinical Profile of von Willebrand Disease in Spain Cohort

    THROMBOSIS AND HAEMOSTASIS . 120(3): 437-448. Nº de cites: 2

    [doi:10.1055/s-0040-1702227]

  • Viñas-Giménez L, Donadeu L, Alsina L, Rincón R, de la Campa EÁ, Esteve-Solé A, Català-Temprano A, Colobran R, de la Cruz X, Sayós J and Martínez-Gallo M.

    Molecular analysis of the novel L243R mutation in STXBP2 reveals impairment of degranulation activity

    INTERNATIONAL JOURNAL OF HEMATOLOGY . 111(3): 440-450. Nº de cites: 3

    [doi:10.1007/s12185-019-02796-7]

  • Ramis-Zaldivar JE, Gonzalez-Farre B, Balagué O, Celis-Passini V, Nadeu F, Salmeron-Villalobos J, Andres M, Martin-Guerrero I, Garrido-Pontnou M, Gaafar A, Suñol M, Barcena C, Garcia-Bragado F, Andión M, Azorín D, Astigarraga I, Sagaseta de Ilurdoz M, Sábado C, Gallego S, Verdu-Amorós J, Fernandez-Delgado R, Perez V, Tapia G, Mozos A, Torrent M, Solano-Páez P, Rivas-Delgado A, Dlouhy I, Clot G, Enjuanes A, López-Guillermo A, Galera PK, Oberley MJ, Maguire A, Ramsower C, Rimsza LM, Quintanilla-Martinez L, Jaffe ES, ELENA CAMPO and Salaverria I.

    Distinct molecular profile of IRF4-rearranged large B-cell lymphoma

    Blood . 135(4): 274-286. Nº de cites: 77

    [doi:10.1182/blood.2019002699]

  • Zanetti SR, Romecin PA, Vinyoles M, Juan-Otero M, Fuster JL, Camós-Guijosa M, Querol S, Delgado M and Menendez P.

    Bone marrow MSC from pediatric patients with B-ALL highly immunosuppress T-cell responses but do not compromise CD19-CAR T-cell activity

    Journal for ImmunoTherapy of Cancer . 8(2): . Nº de cites: 15

    [doi:10.1136/jitc-2020-001419]

  • Ramírez MJ, Minguillón J, Loveless S, Lake K, Carrasco E, Stjepanovic N, Balmaña J, Català-Temprano A, Mehta PA and Surrallés J.

    Chromosome fragility in the buccal epithelium in patients with Fanconi anemia

    CANCER LETTERS . 472: 1-7. Nº de cites: 11

    [doi:10.1016/j.canlet.2019.12.008]