Investigación

Enfermedades Infecciosas y Microbioma

Buscador de publicaciones

Publicaciones

  • Natera-De Benito D, Poo P, Gean Molins E, Vicente-Villa MA, Garcia-Cazorla A and Fons-Estupina C.

    Diploid/triploid mosaicism: a variable but characteristic phenotype

    REVISTA DE NEUROLOGIA . 59(4): 158-163.

    [doi:10.33588/rn.5904.2014077]

  • Pau-Charles I, Vicente-Villa MA, Jou-Munoz C and González-Enseñat MA.

    Acquired hypopigmented suprapubic macules

    CLINICAL AND EXPERIMENTAL DERMATOLOGY . 39(5): 655-657. Nº de citas: 1

    [doi:10.1111/ced.12319]

  • Hernandez-Martin, A, Gilliam, AE, Baselga E, Vicente-Villa MA, Lam, J, Gonzalez-Ensenat, MA, Azorin, D and Torrelo, A.

    Hyperpigmented macules on the face of young children: A series of 25 cases

    JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY . 70(2): 288-290. Nº de citas: 6

    [doi:10.1016/j.jaad.2013.10.045]

  • Carrera J, Albert A, FRANCISCO J PARRI FERRANDIS, Vicente-Villa MA, Brualla D, Rovira-Zurriaga C and Manzano ML.

    [Surgical treatment of giant congenital melanocytic nevi: a change of aim].

    Cirugia pediatrica : organo oficial de la Sociedad Espanola de Cirugia Pediatrica . 27(1): 36-42. Nº de citas: 5

  • 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 citas: 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 citas: 198

    [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 citas: 29

    [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 citas: 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 citas: 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 citas: 7

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