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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: puertas martin v. 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.
Amyloid pet in primary progressive aphasia: case series and systematic review of the literature.
Villarejo-Galende A, Llamas-Velasco S, Gómez-Grande A, Puertas-Martín V, Contador I, Sarandeses P, González-Sánchez M, Trincado R, Pilkington P, Ruiz-Solis S, Pérez-Martínez DA, Herrero-San Martín A. Villarejo-Galende A, et al. Among authors: puertas martin v. J Neurol. 2017 Jan;264(1):121-130. doi: 10.1007/s00415-016-8324-8. Epub 2016 Nov 4. J Neurol. 2017. PMID: 27815682 Review.
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. Among authors: puertas martin v. Neurocase. 2018 Oct-Dec;24(5-6):301-305. doi: 10.1080/13554794.2019.1581225. Epub 2019 Feb 16. Neurocase. 2018. PMID: 30773994 Review.
Decreased salivary lactoferrin levels are specific to Alzheimer's disease.
González-Sánchez M, Bartolome F, Antequera D, Puertas-Martín V, González P, Gómez-Grande A, Llamas-Velasco S, Herrero-San Martín A, Pérez-Martínez D, Villarejo-Galende A, Atienza M, Palomar-Bonet M, Cantero JL, Perry G, Orive G, Ibañez B, Bueno H, Fuster V, Carro E. González-Sánchez M, et al. Among authors: puertas martin v. EBioMedicine. 2020 Jul;57:102834. doi: 10.1016/j.ebiom.2020.102834. Epub 2020 Jun 22. EBioMedicine. 2020. PMID: 32586758 Free PMC article.
Early-Onset Dementia Associated with a Heterozygous, Nonsense, and de novo Variant in the MBD5 Gene.
González-Ortega G, Llamas-Velasco S, Arteche-López A, Quesada-Espinosa JF, Puertas-Martín V, Gómez-Grande A, López-Álvarez J, Saiz Díaz RA, Lezana-Rosales JM, Villarejo-Galende A, González de la Aleja J. González-Ortega G, et al. Among authors: puertas martin v. J Alzheimers Dis. 2021;84(1):73-78. doi: 10.3233/JAD-210648. J Alzheimers Dis. 2021. PMID: 34459404
31 results