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Browsing by Author Torrelo, Antonio

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closedAccessaccesoRestringido.pdf.jpg2016Cutaneous manifestations in patients with mastocytosis: Consensus report of the European Competence Network on Mastocytosis; The American Academy of Allergy, Asthma & Immunology; And the European Academy of Allergology and Clinical ImmunologyHartmann, Karin; Escribano, Luis; Grattan, Clive; Brockow, Knut; Carter, Melody C.; Álvarez-Twose, Iván; Matito, Almudena; Broesby-Olsen, Sigurd; Siebenhaar, Frank; Lange, Magdalena; Niedoszytko, Marek; Castells, Mariana; Oude Elberink, Joanna N. G.; Bonadonna, Patrizia; Zanotti, Roberta; Hornick, Jason L.; Torrelo, Antonio; Grabbe, Jürgen; Rabenhorst, Anja; Nedoszytko, Boguslaw; Butterfield, Joseph H.; Gotlib, Jason; Reiter, Andreas; Radia, Deepti; Hermine, Olivier; Sotlar, Karl; George, Tracy I.; Kristensen, Thomas K.; Kluin-Nelemans, Hanneke C.; Yavuz, Selim; Hägglund, Hans; Sperr, Wolfgang R.; Schwartz, Lawrence B.; Triggiani, Massimo; Maurer, Marcus; Nilsson, Gunnar; Horny, Hans-Peter; Arock, Michel; Orfao, Alberto  ; Metcalfe, Dean D.; Akin, Cem; Valent, PeterArtículo
closedAccessaccesoRestringido.pdf.jpg2014Early-onset acral basal cell carcinomas in Gorlin syndromeTorrelo, Antonio; Bueno, Elena; González-Sarmiento, Rogelio  ; Hernández-Martín, AngelaArtículo
closedAccessaccesoRestringido.pdf.jpg2013Molecular evidence of type 2 mosaicism in Gorlin syndromeTorrelo, Antonio; Hernández-Martín, Angela; González-Sarmiento, Rogelio  Artículo
closedAccessaccesoRestringido.pdf.jpg2012Prevalence of autosomal recessive congenital ichthyosis: A population-based study using the capture-recapture method in SpainHernández-Martín, Angela; Ciria, S.; González-Sarmiento, Rogelio  ; Torrelo, AntonioArtículo
closedAccess3-Nov-2009The H syndrome: Two novel mutations affecting the same amino acid residue of hENT3Molho-Pessach, Vered; Suarez, José; Perrin, Christophe; Chiaverini, Christine; Doviner, Victoria; Tristán Clavijo, E. ; Colmenero, Isabel; Giuliano, Fabienne; Torrelo, Antonio; Zlotogorski, AbrahamArtículo
closedAccessaccesoRestringido.pdf.jpg2016Two cases of autosomal recessive congenital ichthyosis due to CYP4F22 mutations: Expanding the genotype of self-healing collodion babyNoguera-Morel, Lucero; Feito-Rodríguez, Marta; Maldonado-Cid, Paola; García-Miñáur, Sixto; Kamsteeg, Erik-Jan; González-Sarmiento, Rogelio  ; De Lucas-Laguna, Raúl; Hernández-Martín, Angela; Torrelo, AntonioArtículo