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Malalties infeccioses i microbioma

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Publicacions

  • Echeverría-García B, Vicente-Villa MA, Hernández A, Mascaró JM, Colmenero I, Terrón A, Escámez MJ, Del Río M, González-Enseñat MA and Torrelo A.

    Epidermolysis Bullosa Simplex with Mottled Pigmentation: A Family Report and Review

    PEDIATRIC DERMATOLOGY . 30(6): 125-131. Nº de cites: 11

    [doi:10.1111/j.1525-1470.2012.01748.x]

  • Hernández-Martin A, de Lucas R, Vicente-Villa MA, Baselga E, Morcillo-Makow E, Arroyo Manzanal MI, Abaitua I and Torrelo A.

    Reference centers for epidermolysis bullosa and ichthyosis: an urgent need in Spain.

    ACTAS DERMO-SIFILIOGRAFICAS . 104(5): 363-366. Nº de cites: 4

    [doi:10.1016/j.adengl.2013.04.001]

  • Martinez-Martinez L, Vazquez-Ortiz M, Gonzalez-Santesteban C, Martin-Nalda A, Vicente-Villa MA, Plaza-Martín AM, Badell I, Alsina L and de la Calle-Martin O.

    From Severe Combined Immunodeficiency to Omenn syndrome after hematopoietic stem cell transplantation in a RAG1 deficient family

    PEDIATRIC ALLERGY AND IMMUNOLOGY . 23(7): 660-666. Nº de cites: 7

    [doi:10.1111/j.1399-3038.2012.01339.x]

  • Lacruz G, González-Enseñat MA, Suñol M and Vicente-Villa MA.

    Unknown: a congenital nodule on the scapula.

    Dermatology Online Journal . 18(10): 12-12.

  • Hernández-Martín A, Garcia-Doval I, Aranegui B, de Unamuno P, Rodríguez-Pazos L, González-Enseñat MA, Vicente-Villa MA, Martín-Santiago A, Garcia-Bravo B, Feito M, Baselga E, Círia S, de Lucas R, Ginarte M, González-Sarmiento R and Torrelo A.

    Prevalence of autosomal recessive congenital ichthyosis: A population-based study using the capture-recapture method in Spain

    JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY . 67(2): 240-244. Nº de cites: 43

    [doi:10.1016/j.jaad.2011.07.033]

  • Galve J, Vicente-Villa MA, González-Enseñat MA, Pérez-Dueñas B, Cusi V, Møller LB, Julià M, Domínguez A and Ferrando J.

    Neonatal Erythroderma as a First Manifestation of Menkes Disease

    Pediatrics . 130(1): 239-242. Nº de cites: 6

    [doi:10.1542/peds.2011-1558]

  • Hafner, C, Toll, A, Gantner, S, Mauerer, A, Lurkin, I, Acquadro, F, Fernandez-Casado, A, Zwarthoff, EC, Dietmaier, W, Baselga E, Parera, E, Vicente-Villa MA, Casanova, A, Cigudosa, J, Mentzel, T, Pujol, RM, Landthaler, M and Real, FX.

    Keratinocytic epidermal nevi are associated with mosaic RAS mutations

    JOURNAL OF MEDICAL GENETICS . 49(4): 249-253. Nº de cites: 74

    [doi:10.1136/jmedgenet-2011-100637]

  • Guinovart RM, Vicente-Villa MA, Rovira-Zurriaga C, Suñol M and González-Enseñat MA.

    Facial telangiectasia: an unusual manifestation of neonatal lupus erythematosus

    Lupus . 21(5): 552-555. Nº de cites: 8

    [doi:10.1177/0961203311430701]

  • Darwich E, Vicente-Villa MA, Bolling MC, González-Enseñat MA, Cusi V, Fortuny-Guasch C, Bombí JA, Jonkman MF and Mascaró JM.

    Extensive acantholysis as the major histological feature of a severe case of Dowling Meara-epidermolysis bullosa simplex: a reappraisal of acantholysis in the newborn

    EUROPEAN JOURNAL OF DERMATOLOGY . 21(6): 966-971. Nº de cites: 5

    [doi:10.1684/ejd.2011.1497]

  • García M, Santiago JL, Terrón A, Hernández-Martín A, Vicente-Villa MA, Fortuny-Guasch C, De Lucas R, López JC, Cuadrado-Corrales N, Holguín A, Illera N, Duarte B, Sánchez-Jimeno C, Llames S, García E, Ayuso C, Martínez-Santamaría L, Castiglia D, De Luca N, Torrelo A, Mechan D, Baty D, Zambruno G, Escámez MJ and Del Río M.

    Two novel recessive mutations in KRT14 identified in a cohort of 21 Spanish families with epidermolysis bullosa simplex

    BRITISH JOURNAL OF DERMATOLOGY . 165(3): 683-692. Nº de cites: 19

    [doi:10.1111/j.1365-2133.2011.10428.x]