Mostrando 10 resultados de: 22
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scopus(22)
Comedo-like openings in dermoscopy: An essential diagnostic clue for lichen sclerosus, even in children
ArticleAbstract:Palabras claves:Autores:Campos-Domínguez M., Conde-Montero E., Horcajada-Reales C., Parra-Blanco V., Ricardo Maria Suárez-FernándezFuentes:scopusAntibodies to the amino-terminal domain of desmoglein 1 are retained during transition from pemphigus vulgaris to pemphigus foliaceus
ArticleAbstract: Background: Pemphigus vulgaris (PV) and pemphigus foliaceus (PF) are two blistering skin diseases mePalabras claves:Acantholysis, Desmoglein, Desmoglein domain-swapped molecules, Immunoblotting/immunoprecipitation, Pemphigus foliaceus, Pemphigus vulgarisAutores:España A., Hashimoto T., Irarrazaval I., Ishii N., Koga H., Ohata C., Ohyama B., Ricardo Maria Suárez-Fernández, Teye K.Fuentes:scopusConcordance analysis of dermoscopic features between five observers in a sample of 200 dermoscopic images
ArticleAbstract:Palabras claves:Autores:Avilés-Izquierdo J.A., Masdemont B.L., Nieto-Benito L.M., Ricardo Maria Suárez-Fernández, Rodríguez-Lomba E., Torre E.H.d.l.Fuentes:scopusDenuded areas of skin in an infant
ArticleAbstract:Palabras claves:Autores:Campos-Domínguez M., Molina-Lopez I., Ricardo Maria Suárez-Fernández, Rodríguez-Lomba E.Fuentes:scopusAcquired trichorrhexis nodosa in a young black woman
ArticleAbstract:Palabras claves:Autores:Barchino-Ortiz L., Cabeza-Martínez R., Manuel Leis-Dosil V., Ricardo Maria Suárez-FernándezFuentes:scopusAcute generalized blistering eruption in a 4-month-old infant
OtherAbstract:Palabras claves:Autores:Barchino-Ortiz L., Cano-Martinez N., Ricardo Maria Suárez-FernándezFuentes:scopusFiliform Follicular Hyperkeratosis on the Face
ArticleAbstract:Palabras claves:Autores:Campos Domíngez M., Parra-Blanco V., Ricardo Maria Suárez-Fernández, Ruiz-Rivero J.Fuentes:scopusFlat-topped papules on the face of a young boy
ArticleAbstract:Palabras claves:Autores:Campos-Domínguez M., Ricardo Maria Suárez-Fernández, Vilas-Boas P.Fuentes:scopusEctodermal dysplasia with congenital adermatoglyphia (Basan syndrome): Report of two cases presenting with extensive congenital milia
ArticleAbstract: Basan syndrome is a rare autosomal dominant genodermatosis, characterized by rapidly healing congeniPalabras claves:adermatoglyphia, Basan syndrome, ectodermal dysplasia, GenodermatosisAutores:Campos-Domínguez M., Feito-Rodríguez M., Martínez-González V., Molina-Lopez I., Nieto-Benito L.M., Ricardo Maria Suárez-FernándezFuentes:scopusNeonatal ichthyosis and hypotrichosis
OtherAbstract:Palabras claves:Autores:Campos-Domínguez M., Ricardo Maria Suárez-Fernández, Sanchez-Herrero A., Vilas-Boas P.Fuentes:scopus