Personas / Equipo Humano

Anna Ruiz Llobet

Buscador de publicaciones

Publicaciones

  • Pérez-Grijalba V, Arbizu J, Romero J, Prieto E, Pesini P, Sarasa L, Guillen F, Monleón I, San-José I, Martínez-Lage P, Munuera-del Cerro JL, Hernández I, Buendía M, Sotolongo-Grau O, Alegret M, Ruiz-Llobet A, Tárraga L, Boada M and Sarasa M.

    Plasma A beta 42/40 ratio alone or combined with FDG-PET can accurately predict amyloid-PET positivity: a cross-sectional analysis from the AB255 Study

    ALZHEIMERS RESEARCH & THERAPY . 11(1): 96-96. Nº de citas: 49

    [doi:10.1186/s13195-019-0549-1]

  • Arias-Salgado EG, Galvez E, Planas-Cerezales L, Pintado-Berninches L, Vallespin E, Martinez P, Carrillo J, Iarriccio L, Ruiz-Llobet A, Català-Temprano A, Badell-Serra I, Gonzalez-Granado LI, Martín-Nalda A, Martínez-Gallo M, Galera-Miñarro A, Rodríguez-Vigil C, Bastos-Oreiro M, Perez de Nanclares G, Leiro-Fernández V, Uria ML, Diaz-Heredia C, Valenzuela C, Martín S, López-Muñiz B, Lapunzina P, Sevilla J, Molina-Molina M, Perona R and Sastre L.

    Genetic analyses of aplastic anemia and idiopathic pulmonary fibrosis patients with short telomeres, possible implication of DNA-repair genes.

    ORPHANET JOURNAL OF RARE DISEASES . 14(1): 82-82. Nº de citas: 25

    [doi:10.1186/s13023-019-1046-0]

  • Vega-García N, Malatesta R, Estella-Aguado MC, Pérez-Jaume S, Esperanza-Cebollada E, Torrebadell-Burriel M, Català-Temprano A, Gassiot S, Berrueco R, Ruiz-Llobet A, Alonso-Saladrigues A, Mesegue-Meda M, Pont-Martí S, Rives-Solà S and Camós-Guijosa M.

    Paediatric patients with acute leukaemia and KMT2A (MLL) rearrangement show a distinctive expression pattern of histone deacetylases

    BRITISH JOURNAL OF HAEMATOLOGY . 182(4): 542-553. Nº de citas: 9

    [doi:10.1111/bjh.15436]

  • Llaudet-Planas E, Vives-Corrons JL, Rizzuto V, Gómez-Ramírez P, Sevilla Navarro J, Coll Sibina MT, García-Bernal M, Ruiz-Llobet A, Badell-Serra I, Velasco-Puyó P, Dapena JL and Mañú-Pereira MM.

    Osmotic gradient ektacytometry: A valuable screening test for hereditary spherocytosis and other red blood cell membrane disorders.

    INT J LAB HEMATOL . 40(1): 94-102. Nº de citas: 62

    [doi:10.1111/ijlh.12746]

  • Cela E, Bellón JM, de la Cruz M, Beléndez C, Berrueco R, Ruiz-Llobet A, Elorza I, Díaz de Heredia C, Cervera A, Vallés G, Salinas JA, Coll MT, Bermúdez M, Prudencio M, Argilés B and Vecilla C.

    National registry of hemoglobinopathies in Spain (REPHem)

    PEDIATRIC BLOOD & CANCER . 64(7): . Nº de citas: 36

    [doi:10.1002/pbc.26322]

  • Berrueco R, Alonso-Saladrigues A, Martorell-Sampol L, Català-Temprano A, Ruiz-Llobet A, Toll T, Torrebadell-Burriel M, Naudo-Lahoz M, Camós-Guijosa M and Rives-Solà S.

    Outcome and toxicities associated to chemotherapy in children with acute lymphoblastic leukemia and Gilbert syndrome. Usefulness of UGT1A1 mutational screening

    PEDIATRIC BLOOD & CANCER . 62(7): 1195-1201. Nº de citas: 8

    [doi:10.1002/pbc.25457]

  • Berrueco R, Antón A, Rives-Solà S, Català-Temprano A, Toll T, Ruiz-Llobet A, Camós-Guijosa M, Torrebadell-Burriel M, Estella J and Munoz-Almagro C.

    Multiplex real-time PCR for prompt diagnosis of an outbreak of human parainfluenza 3 virus in children with acute leukemia

    Infection . 41(6): 1171-1175. Nº de citas: 7

    [doi:10.1007/s15010-013-0498-8]

  • Berrueco R, Rives-Solà S, Català-Temprano A, Toll T, Gene-Giralt A, Ruiz-Llobet A, Badosa R, Claramonte MA, Estella J and Urrea M.

    Prospective Surveillance Study of Blood Stream Infections Associated With Central Venous Access Devices (Port-type) in Children With Acute Leukemia: An Intervention Program

    JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY . 35(5): 194-199. Nº de citas: 22

    [doi:10.1097/MPH.0b013e318290c24f]