Persones / Equip Humà

Cecilia Jiménez Mallebrera

Buscador de publicacions

Publicacions

  • Jimenez-Mallebrera C, Davies K, Putt W and Edwards YH.

    A study of short utrophin isoforms in mice deficient for full-length utrophin

    MAMMALIAN GENOME . 14(1): 47-60. Nº de cites: 16

    [doi:10.1007/s00335-002-3044-z]

  • Jimenez-Mallebrera C, Torelli S, Brown SC, Feng L, Brockington M, Sewry CA, Beltrán-Valero De Bernabé D and Muntoni F.

    Profound skeletal muscle depletion of a-dystroglycan in Walker-Warburg syndrome

    EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY . 7(3): 129-137. Nº de cites: 30

    [doi:10.1016/S1090-3798(03)00042-4]

  • Wilson J, Putt W, Jimenez-Mallebrera C and Edwards YH.

    Up71 and Up140, two novel transcripts of utrophin that are homologues of short forms of dystrophin

    HUMAN MOLECULAR GENETICS . 8(7): 1271-1278. Nº de cites: 46

    [doi:10.1093/hmg/8.7.1271]

  • Villar-Quiles RN, Foley AR, Metay C, Orbach R, Donkervoort S, Labella B, Natera-de Benito D, Nascimento-Osorio A, Estévez-Arias B, Jimenez-Mallebrera C, Ortez-Gonzalez CI, Domínguez-González C, Horga A, Marti Carrera MI, Fernandez Torron R, Kurbatov S, Chausova P, Murtazina A, Subbotin D, Kuchina A, Frezzati R, Carvalho A, Waschbisch A, Allamand V, Zou Y, Richard P, Bönnemann CG and Stojkovic T.

    Expanding the phenotypic spectrum of COL6-related diseases: Motor neuropathy-like and neuromyopathy associated with COL6A3 c.7447A>G.

    Journal of Neuromuscular Diseases . : .

    [doi:10.1177/22143602261453996]