Personas / Equipo Humano

Susana Rives Solà

Buscador de publicaciones

Publicaciones

  • 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]

  • Carrillo J, Martínez P, Solera J, Moratilla C, González A, Manguán-García C, Aymerich M, Canal L, Del Campo M, Dapena JL, Escoda L, García-Sagredo JM, Martín-Sala S, Rives-Solà S, Sevilla J, Sastre L and Perona R.

    High resolution melting analysis for the identification of novel mutations in DKC1 and TERT genes in patients with dyskeratosis congenita

    BLOOD CELLS MOLECULES AND DISEASES . 49(3-4): 140-146. Nº de citas: 27

    [doi:10.1016/j.bcmd.2012.05.008]

  • Salazar J, Altés A, del Río E, Estella J, Rives-Solà S, Tasso M, Navajas A, Molina J, Villa M, Vivanco JL, Torrent M, Baiget M and Badell I.

    Methotrexate consolidation treatment according to pharmacogenetics of MTHFR ameliorates event-free survival in childhood acute lymphoblastic leukaemia

    PHARMACOGENOMICS JOURNAL . 12(5): 379-385. Nº de citas: 48

    [doi:10.1038/tpj.2011.25]

  • Garcia-Puig M, Fons-Estupina MC, Rives-Solà S, Berrueco-Moreno R, Cruz-Martínez O and Campistol-Plana J.

    Neurotoxicity due to methotrexate in paediatric patients. Description of the clinical symptoms and neuroimaging findings

    REVISTA DE NEUROLOGIA . 54(12): 712-718. Nº de citas: 9

    [doi:10.33588/rn.5412.2012005]

  • Rives-Solà S, Estella J, Camós-Guijosa M, García-Miguel P, Verdeguer A, Couselo JM, Tasso M, Molina J, Gómez P, Fernández-Delgado R, Navajas A and Badell I.

    T-cell pediatric acute lymphoblastic leukemia: analysis of survival and prognostic factors in 4 consecutive protocols of the Spanish cooperative study group SHOP

    MEDICINA CLINICA . 139(4): 141-149. Nº de citas: 8

    [doi:10.1016/j.medcli.2011.12.019]

  • Rives-Solà S, Estella J, Gómez P, López-Duarte M, de Miguel PG, Verdeguer A, Moreno MJ, Vivanco JL, Couselo JM, Fernández-Delgado R, Maldonado M, Tasso M, López-Ibor B, Lendinez F, López-Almaraz R, Uriz J, Melo M, Fernández-Teijeiro A, Rodríguez I and Badell I.

    Intermediate dose of imatinib in combination with chemotherapy followed by allogeneic stem cell transplantation improves early outcome in paediatric Philadelphia chromosome-positive acute lymphoblastic leukaemia (ALL): results of the Spanish Cooperative Group SHOP studies ALL-94, ALL-99 and ALL-2005

    BRITISH JOURNAL OF HAEMATOLOGY . 154(5): 600-611. Nº de citas: 51

    [doi:10.1111/j.1365-2141.2011.08783.x]

  • Launes-Montana C, Rives-Solà S, Català A, Berrueco R, Toll T, Camós-Guijosa M, Munoz-Almagro C, García-García JJ and Estella J.

    Pandemic influenza A (2009 H1N1) in children with acute lymphoblastic leukaemia

    BRITISH JOURNAL OF HAEMATOLOGY . 149(6): 874-878. Nº de citas: 27

    [doi:10.1111/j.1365-2141.2010.08178.x]

  • Berrueco R, Rives-Solà S, Camós-Guijosa M, Toll T, Català-Temprano A and Estella J.

    Syndromic albinism and haemophagocytosis.

    BRITISH JOURNAL OF HAEMATOLOGY . 148(6): 815-815. Nº de citas: 3

    [doi:10.1111/j.1365-2141.2009.07885.x]

  • Rives-Solà S, Pahl HL, Florensa L, Bellosillo B, Neusuess A, Estella J, Debatin KM, Kohne E, Schwarz K and Cario H.

    Molecular genetic analyses in familial and sporadic congenital primary erythrocytosis

    HAEMATOLOGICA . 92(5): 674-677. Nº de citas: 26

    [doi:10.3324/haematol.10787]

  • Rives-Solà S, Alcorta I, Toll T, Tuset E, Estella J and Cross NC.

    Idiopathic hypereosinophilic syndrome in children - Report of a 7-year-old boy with FIP1L1-PDGFRA rearrangement

    JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY . 27(12): 663-665. Nº de citas: 33

    [doi:10.1097/01.mph.0000193467.06938.77]