Personas / Equipo Humano

Ferran Torner Rubies

Buscador de publicaciones

Publicaciones

  • Pérez-López LM, Vara-Patudo I, Torner-Rubies F, Tenorio V, Cabo LS, Fortuny-Guasch C and Knörr G.

    Pediatric Psoas Abscess, Early Diagnosis of a Challenging Condition.

    Journal of Acute Medicine . 7(4): 158-166. Nº de citas: 4

    [doi:10.6705/j.jacme.2017.0704.004]

  • Soldado, F., Diaz-Gallardo, P., Lidia, S.-C., Torner-Rubies F, Josep, B.-D., Mascarenhas, V.V. and Knorr, J..

    Vascularized fibular grafts extended with vascularized periosteum in children.

    MICROSURGERY . 37(5): 410-415. Nº de citas: 16

    [doi:10.1002/micr.30063]

  • Goepel U, Torner-Rubies F and Soldado F.

    Neuromuscular choriostoma of brachial plexus in a boy: A case report.

    Journal Of Hand Surgery-British And European Volume . 42(5): 531-532. Nº de citas: 3

    [doi:10.1177/1753193416656100]

  • Torner-Rubies F, Segur JM, Rosendo Ullot Font, Soldado F, Domenech P, DeSena L and Knorr J.

    Non-invasive expandable prosthesis in musculoskeletal oncology paediatric patients for the distal and proximal femur. First results.

    INTERNATIONAL ORTHOPAEDICS . 40(8): 1683-1688. Nº de citas: 27

    [doi:10.1007/s00264-016-3163-x]

  • Kalko SG, Paco-Mercader S, Jou-Munoz C, Rodríguez MA, Meznaric M, Rogac M, Jekovec-Vrhovsek M, Sciacco M, Moggio M, Fagiolari G, De Paepe B, De Meirleir L, Ferrer I, Roig-Quilis M, Munell F, Montoya J, López-Gallardo E, Ruiz-Pesini E, Artuch-Iriberri R, Montero-Sanchez R, Torner-Rubies F, Nascimento-Osorio A, Ortez-Gonzalez CI, Colomer J and Jimenez-Mallebrera C.

    Transcriptomic profiling of TK2 deficient human skeletal muscle suggests a role for the p53 signalling pathway and identifies growth and differentiation factor-15 as a potential novel biomarker for mitochondrial myopathies

    BMC Genomics . 15: 91-91. Nº de citas: 108

    [doi:10.1186/1471-2164-15-91]

  • Paco-Mercader S, Kalko SG, Jou-Munoz C, Rodríguez MA, Corbera J, Muntoni F, Feng L, Rivas E, Torner-Rubies F, Gualandi F, Gomez-Foix AM, Ferrer A, Ortez-Gonzalez CI, Nascimento-Osorio A, Colomer J and Jimenez-Mallebrera C.

    Gene Expression Profiling Identifies Molecular Pathways Associated with Collagen VI Deficiency and Provides Novel Therapeutic Targets

    PLoS One . 8(10): . Nº de citas: 21

    [doi:10.1371/journal.pone.0077430]

  • Celis-Passini V, de Torres C, Parareda A, Rodriguez N, Torner-Rubies F, Cruz-Martínez O and Mora J.

    Treatment of Newly Diagnosed Ewing Sarcoma with Gemcitabine and Docetaxel as an Alternative to Conventional Therapy in 2 patients Who Did Not Wish to Undergo Intensive Chemotherapy

    Oncopedia . : 584.

  • Sarrión P, Sangorrin A, Urreizti R, Delgado A, Artuch-Iriberri R, Martorell-Sampol L, Armstrong-Moron J, Anton-Lopez J, Torner-Rubies F, Vilaseca MA, Nevado J, Lapunzina P, Asteggiano CG, Balcells S and Grinberg D.

    Mutations in the EXT1 and EXT2 genes in Spanish patients with multiple osteochondromas

    SCIENTIFIC REPORTS . 3: 1346-1346. Nº de citas: 49

    [doi:10.1038/srep01346]

  • Paco-Mercader S, Ferrer I, Jou-Munoz C, Cusi V, Corbera J, Torner-Rubies F, Gualandi F, Sabatelli P, Orozco A, Gómez-Foix AM, Colomer J, Nascimento-Osorio A and Jimenez-Mallebrera C.

    Muscle Fiber Atrophy and Regeneration Coexist in Collagen VI-Deficient Human Muscle: Role of Calpain-3 and Nuclear Factor-?B Signaling

    JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY . 71(10): 894-906. Nº de citas: 23

    [doi:10.1097/NEN.0b013e31826c6f7b]

  • Jimenez-Mallebrera C, Paco-Mercader S, Kalko S, Jou-Munoz C, Rodríguez-García MA, Cusi V, Joan R. Corbera Torredeflò, Colomer J, Nascimento-Osorio A and Torner-Rubies F.

    Perfil de expresión génica en la distrofia muscular congénita de Ullrich

    REVISTA DE NEUROLOGIA . 2012(27): 155-312.