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104 results

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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.
Hernandez-Martín A, Aranegui B, Escámez MJ, de Lucas R, Vicente A, Rodríguez-Díaz E, Bernabeu-Wittel J, Gonzalez-Hermosa R, García-Patos V, Ginarte M, Mascaró JM Jr, Corredera C, Baselga E, Santiago JL, Chaves A, Román C, Evole M, Martin-Santiago A, Torrelo A, Del Río M, Feito M, Gonzalez-Enseñat MA, Romero G, Morcillo-Makow E, Abaitua I, García-Doval I. Hernandez-Martín A, et al. Among authors: feito m. Actas Dermosifiliogr. 2013 Dec;104(10):890-6. doi: 10.1016/j.ad.2013.03.006. Epub 2013 Jun 27. Actas Dermosifiliogr. 2013. PMID: 23809583 Free article.
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
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.
Capillary malformation-arteriovenous malformation syndrome: a multicentre study.
Valdivielso-Ramos M, Martin-Santiago A, Azaña JM, Hernández-Nuñez A, Vera A, Perez B, Tercedor J, Feito M, Vicente A, Prat C, Lopez-Gutierrez JC, Garnacho G, Baselga E, Roe E, Palencia S, Cordero P, Moreno R, Agudo A, de la Cueva P, Torrelo A. Valdivielso-Ramos M, et al. Among authors: feito m. Clin Exp Dermatol. 2021 Mar;46(2):300-305. doi: 10.1111/ced.14428. Epub 2020 Oct 20. Clin Exp Dermatol. 2021. PMID: 32840927
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
104 results