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Expanding the clinical and genetic spectrum of SQSTM1-related disorders in family with personality disorder and frontotemporal dementia.
Llamas-Velasco S, Arteche-López A, Méndez-Guerrero A, Puertas Martín V, Quesada Espinosa JF, Lezana Rosales JM, González-Sánchez M, Blanco-Palmero VA, Palma Milla C, Herrero-San Martín A, Borrego-Hernández D, García-Redondo A, Pérez-Martínez DA, Villarejo-Galende A. Llamas-Velasco S, et al. Among authors: mendez guerrero a. Amyotroph Lateral Scler Frontotemporal Degener. 2021 Nov;22(7-8):552-560. doi: 10.1080/21678421.2021.1927101. Epub 2021 May 19. Amyotroph Lateral Scler Frontotemporal Degener. 2021. PMID: 34009082 Review.
Brain-to-brain embolism: an unknown pathway to consider in ischemic strokes.
López-Blanco R, Díaz-Guzmán J, Méndez-Guerrero A, de Fuenmayor-Fernández de la Hoz CP, González-Sánchez M, Llorente-Ayuso L, Gredilla-Zubiria Í, Calleja-Castaño P. López-Blanco R, et al. Rev Neurol. 2015 Dec 1;61(11):509-10. Rev Neurol. 2015. PMID: 26602806 Free article. English, Spanish. 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.
Acute hypokinetic-rigid syndrome following SARS-CoV-2 infection.
Méndez-Guerrero A, Laespada-García MI, Gómez-Grande A, Ruiz-Ortiz M, Blanco-Palmero VA, Azcarate-Diaz FJ, Rábano-Suárez P, Álvarez-Torres E, de Fuenmayor-Fernández de la Hoz CP, Vega Pérez D, Rodríguez-Montalbán R, Pérez-Rivilla A, Sayas Catalán J, Ramos-González A, González de la Aleja J. Méndez-Guerrero A, et al. Neurology. 2020 Oct 13;95(15):e2109-e2118. doi: 10.1212/WNL.0000000000010282. Epub 2020 Jul 8. Neurology. 2020. PMID: 32641525
First patient with mosaic NOTCH3 gene pathogenic variant. Unrevealed mosaicisms and importance of their detection.
Moreno-García M, Arteche-López AR, Álvarez-Mora MI, Palma Milla C, Quesada Espinosa JF, Lezana Rosales JM, Sánchez Calvín MT, Gómez Manjón I, Gómez Rodríguez MJ, Mendez-Guerrero A, Villarejo-Galende A. Moreno-García M, et al. Am J Med Genet A. 2021 Feb;185(2):591-595. doi: 10.1002/ajmg.a.61999. Epub 2020 Dec 11. Am J Med Genet A. 2021. PMID: 33305890
Serum and CSF alpha-synuclein levels do not change in COVID-19 patients with neurological symptoms.
Blanco-Palmero VA, Azcárate-Díaz FJ, Ruiz-Ortiz M, Laespada-García MI, Rábano-Suárez P, Méndez-Guerrero A, Aramendi-Ramos M, Eguiburu JL, Pérez-Rivilla A, Marchán-López A, Rubio-Fernández M, Carro E, González de la Aleja J. Blanco-Palmero VA, et al. Among authors: mendez guerrero a. J Neurol. 2021 Sep;268(9):3116-3124. doi: 10.1007/s00415-021-10444-6. Epub 2021 Feb 19. J Neurol. 2021. PMID: 33606070 Free PMC article.
31 results