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Sporadic Creutzfeldt-Jakob disease with extremely long 14-year survival period.
Kortazar-Zubizarreta I, Ruiz-Onandi R, Pereda A, Vado Y, González-Chinchon G, Eraña H, Perez de Nanclares G, Castilla J. Kortazar-Zubizarreta I, et al. Among authors: vado y. Eur J Neurol. 2021 Sep;28(9):2901-2906. doi: 10.1111/ene.14946. Epub 2021 Jun 26. Eur J Neurol. 2021. PMID: 34060706 Free PMC article.
Marfan Syndrome Caused by Somatic Mosaicism in an FBN1 Splicing Mutation.
Rekondo J, Robledo-Inarritu M, Vado Y, Pérez de Nanclares G, Arós F. Rekondo J, et al. Among authors: vado y. Rev Esp Cardiol (Engl Ed). 2016 May;69(5):520-1. doi: 10.1016/j.rec.2016.01.018. Epub 2016 Mar 30. Rev Esp Cardiol (Engl Ed). 2016. PMID: 27037046 English, Spanish. No abstract available.
Genetic counselling in the era of next generation sequencing.
Espada-Musitu D, Manero-Azua Á, Vado Y, Perez de Nanclares G. Espada-Musitu D, et al. Among authors: vado y. An Pediatr (Engl Ed). 2025 Jan;102(1):503712. doi: 10.1016/j.anpede.2024.503712. Epub 2024 Dec 31. An Pediatr (Engl Ed). 2025. PMID: 39743412 Free article. Review.