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Hereditary cerebral small vessel disease: Assessment of a HTRA1 variant using protein stability predictors and 3D modelling.
Hidalgo Mayoral I, Martínez-Salio A, Llamas-Velasco S, Gómez-Majón I, Arteche-López A, Quesada-Espinosa JF, Palma Milla C, Lezana Rosales JM, Pérez de la Fuente R, Juárez Rufián A, Sierra Tomillo O, Sánchez Calvín MT, Gómez Rodríguez MJ, Ramos Gómez P, Villarejo-Galende A, Díaz-Guzmán J, Ortega-Casarrubios MÁ, Calleja-Castaño P, Moreno-García M. Hidalgo Mayoral I, et al. Among authors: llamas velasco s. Eur J Med Genet. 2022 Aug;65(8):104539. doi: 10.1016/j.ejmg.2022.104539. Epub 2022 Jun 12. Eur J Med Genet. 2022. PMID: 35705147
Alzheimer's disease prevention: A way forward.
Bermejo-Pareja F, Llamas-Velasco S, Villarejo-Galende A. Bermejo-Pareja F, et al. Rev Clin Esp (Barc). 2016 Dec;216(9):495-503. doi: 10.1016/j.rce.2016.05.010. Epub 2016 Jun 17. Rev Clin Esp (Barc). 2016. PMID: 27325510 English, Spanish.
Enteroviral T-cell encephalitis related to immunosuppressive therapy including rituximab.
Garzo-Caldas N, Ruiz-Sainz E, Vila-Bedmar S, Llamas-Velasco S, Hernández-Lain A, Ruiz-Morales J, Folgueira-López D, Villarejo-Galende A. Garzo-Caldas N, et al. Neurology. 2017 Jul 25;89(4):408-409. doi: 10.1212/WNL.0000000000004148. Epub 2017 Jun 23. Neurology. 2017. PMID: 28645913 Free PMC article. No abstract available.
TARDBP mutation associated with semantic variant primary progressive aphasia, case report and review of the literature.
González-Sánchez M, Puertas-Martín V, Esteban-Pérez J, García-Redondo A, Borrego-Hernández D, Méndez-Guerrero A, Llamas-Velasco S, Herrero-San Martín A, Cordero-Vázquez P, Herrero-Manso MC, Pérez-Martínez DA, Villarejo-Galende A. González-Sánchez M, et al. Neurocase. 2018 Oct-Dec;24(5-6):301-305. doi: 10.1080/13554794.2019.1581225. Epub 2019 Feb 16. Neurocase. 2018. PMID: 30773994 Review.
38 results