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A Novel Splicing Mutation in the ACVRL1/ALK1 Gene as a Cause of HHT2.
Errasti Díaz S, Peñalva M, Recio-Poveda L, Vilches S, Casado-Vela J, Pérez Pérez J, Botella LM, Albiñana V, Cuesta AM. Errasti Díaz S, et al. Among authors: perez perez j. J Clin Med. 2022 May 28;11(11):3053. doi: 10.3390/jcm11113053. J Clin Med. 2022. PMID: 35683441 Free PMC article.
Relevance of complement factor H-related 1 (CFHR1) genotypes in age-related macular degeneration.
Martínez-Barricarte R, Recalde S, Fernández-Robredo P, Millán I, Olavarrieta L, Viñuela A, Pérez-Pérez J, García-Layana A, Rodríguez de Córdoba S; Spanish Multicenter Group on AMD. Martínez-Barricarte R, et al. Among authors: perez perez j. Invest Ophthalmol Vis Sci. 2012 Mar 1;53(3):1087-94. doi: 10.1167/iovs.11-8709. Invest Ophthalmol Vis Sci. 2012. PMID: 22247456 Free article.
Association between CFH, CFB, ARMS2, SERPINF1, VEGFR1 and VEGF polymorphisms and anatomical and functional response to ranibizumab treatment in neovascular age-related macular degeneration.
Cobos E, Recalde S, Anter J, Hernandez-Sanchez M, Barreales C, Olavarrieta L, Valverde A, Suarez-Figueroa M, Cruz F, Abraldes M, Pérez-Pérez J, Fernández-Robredo P, Arias L, García-Layana A. Cobos E, et al. Among authors: perez perez j. Acta Ophthalmol. 2018 Mar;96(2):e201-e212. doi: 10.1111/aos.13519. Epub 2017 Sep 19. Acta Ophthalmol. 2018. PMID: 28926193 Free article.
[No title available]
[No authors listed] [No authors listed] PMID: 35109199
SORL1 Variants in Familial Alzheimer's Disease.
Gómez-Tortosa E, Ruggiero M, Sainz MJ, Villarejo-Galende A, Prieto-Jurczynska C, Venegas Pérez B, Ordás C, Agüero P, Guerrero-López R, Pérez-Pérez J. Gómez-Tortosa E, et al. Among authors: perez perez j. J Alzheimers Dis. 2018;61(4):1275-1281. doi: 10.3233/JAD-170590. J Alzheimers Dis. 2018. PMID: 29376855
251 results