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104 results

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Page 1
Keratosis pilaris-like eruption secondary to nilotinib in a child.
Oro-Ayude M, Feito M, Quintana-Castanedo L, Beato-Merino MJ, De Lucas R. Oro-Ayude M, et al. Among authors: feito m. Pediatr Dermatol. 2020 Sep;37(5):968-969. doi: 10.1111/pde.14267. Epub 2020 Jun 29. Pediatr Dermatol. 2020. PMID: 32602176
Dilated Cardiomyopathy in a Child with Recessive Dystrophic Epidermolysis Bullosa.
Imbernón-Moya A, Maseda-Pedrero R, Feito M, de Lucas R. Imbernón-Moya A, et al. Among authors: feito m. Actas Dermosifiliogr (Engl Ed). 2019 Jan-Feb;110(1):81-83. doi: 10.1016/j.ad.2017.10.025. Epub 2018 Apr 23. Actas Dermosifiliogr (Engl Ed). 2019. PMID: 29699768 English, Spanish. No abstract available.
Prevalence of autosomal recessive congenital ichthyosis: a population-based study using the capture-recapture method in Spain.
Hernández-Martín A, Garcia-Doval I, Aranegui B, de Unamuno P, Rodríguez-Pazos L, González-Enseñat MA, Vicente A, Martín-Santiago A, Garcia-Bravo B, Feito M, Baselga E, Círia S, de Lucas R, Ginarte M, González-Sarmiento R, Torrelo A. Hernández-Martín A, et al. Among authors: feito m. J Am Acad Dermatol. 2012 Aug;67(2):240-4. doi: 10.1016/j.jaad.2011.07.033. Epub 2011 Oct 14. J Am Acad Dermatol. 2012. PMID: 22000705
A six-attribute classification of genetic mosaicism.
Martínez-Glez V, Tenorio J, Nevado J, Gordo G, Rodríguez-Laguna L, Feito M, de Lucas R, Pérez-Jurado LA, Ruiz Pérez VL, Torrelo A, Spinner NB, Happle R, Biesecker LG, Lapunzina P. Martínez-Glez V, et al. Among authors: feito m. Genet Med. 2020 Nov;22(11):1743-1757. doi: 10.1038/s41436-020-0877-3. Epub 2020 Jul 14. Genet Med. 2020. PMID: 32661356 Free PMC article. Review.
Prioritization of therapy uncertainties in Dystrophic Epidermolysis Bullosa: where should research direct to? an example of priority setting partnership in very rare disorders.
Davila-Seijo P, Hernández-Martín A, Morcillo-Makow E, de Lucas R, Domínguez E, Romero N, Monrós E, Feito M, Carretero L, Aranegui B, García-Doval I. Davila-Seijo P, et al. Among authors: feito m. Orphanet J Rare Dis. 2013 Apr 22;8:61. doi: 10.1186/1750-1172-8-61. Orphanet J Rare Dis. 2013. PMID: 23607806 Free PMC article.
104 results