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Publicacions

  • Hernandez-Martín A, Aranegui B, Escámez MJ, de Lucas R, Vicente-Villa MA, Rodríguez-Díaz E, Bernabeu-Wittel J, Gonzalez-Hermosa R, García-Patos V, Ginarte M, Mascaró JM, Corredera C, Baselga E, Santiago JL, Chaves A, Román C, Evole M, Martin-Santiago A, Torrelo A, Del Río M, Feito M, González-Enseñat MA, Romero G, Morcillo-Makow E, Abaitua I and García-Doval I.

    Prevalence of dystrophic epidermolysis bullosa in Spain: a population-based study using the 3-source capture-recapture method. Evidence of a need for improvement in care.

    ACTAS DERMO-SIFILIOGRAFICAS . 104(10): 890-6. Nº de cites: 19

    [doi:10.1016/j.ad.2013.03.006]

  • Revencu N, Boon LM, Mendola A, Cordisco MR, Dubois J, Clapuyt P, Hammer F, Amor DJ, Irvine AD, Baselga E, Dompmartin A, Syed S, Santiago AM, Ades L, Collins F, Smith J, Sandaradura S, Barrio VR, Burrows PE, Blei F, Cozzolino M, Brunetti-Pierri N, Vicente-Villa MA, Abramowicz M, Désir J, Vilain C, Chung WK, Wilson A, Gardiner CA, Dwight Y, Lord DJ, Fishman L, Cytrynbaum C, Chamlin S, Ghali F, Gilaberte Y, Joss S, Boente MD, Léauté-Labrèze C, Delrue MA, Bayliss S, Martorell-Sampol L, Gonzalez MA, Mazereeuw-Hautier J, O'Donnell B, Bessis D, Pyeritz RE, Salhi A, Tan OT, Wargon O, Mulliken JB and Vikkula M.

    RASA1 Mutations and Associated Phenotypes in 68 Families with Capillary Malformation-Arteriovenous Malformation

    HUMAN MUTATION . 34(12): 1632-1641. Nº de cites: 194

    [doi:10.1002/humu.22431]

  • de la Fuente S, Hernández-Martín Á, de Lucas R, González-Enseñat MA, Vicente-Villa MA, Colmenero I, González-Beato M, Suñol M and Torrelo A.

    Postvaccination Bullous Pemphigoid in Infancy: Report of Three New Cases and Literature Review

    PEDIATRIC DERMATOLOGY . 30(6): 741-744. Nº de cites: 28

    [doi:10.1111/pde.12231]

  • 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]