Publicacións en colaboración con investigadores/as de Complexo Hospitalario Universitario de Vigo (10)

2023

  1. Pseudofolliculitis of the breast: Report of five cases

    Australasian Journal of Dermatology

2019

  1. A novel ABCA12 pathologic variant identified in an Ecuadorian harlequin ichthyosis patient: A step forward in genotype-phenotype correlations

    Molecular Genetics and Genomic Medicine, Vol. 7, Núm. 5

  2. Biogeographical origin and timing of the founder ichthyosis TGM1 c.1187G > A mutation in an isolated Ecuadorian population

    Scientific Reports, Vol. 9, Núm. 1

  3. Novel compound heterozygous FATP4 mutations caused ichthyosis prematurity syndrome in Spanish sisters

    Acta Paediatrica, International Journal of Paediatrics, Vol. 108, Núm. 4, pp. 763-765

2018

  1. ABCA12 mutations in patients with autosomal recessive congenital ichthyosis: evidence of a founder effect in the Spanish population and phenotype-genotype implications

    Journal of Dermatological Science

2017

  1. Phenotypic spectrum of autosomal recessive congenital ichthyosis due to PNPLA1 mutation

    British Journal of Dermatology

2011

  1. Reproducibility of the diagnosis of onychomycosis by dermatologists in a clinical setting

    Actas Dermo-Sifiliograficas

2010

  1. Clinical diagnosis of toenail onychomycosis is possible in some patients: Cross-sectional diagnostic study and development of a diagnostic rule

    British Journal of Dermatology, Vol. 163, Núm. 4, pp. 743-751

  2. Molusco contagioso: estudio descriptivo

    Anales de Pediatria, Vol. 72, Núm. 2, pp. 139-142

2009

  1. Observer agreement in toenail disorders: implications for diagnosis and clinical research

    British Journal of Dermatology, Vol. 160, Núm. 6, pp. 1315-1317