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Page 1
Epidemiology of ataxia and hereditary spastic paraplegia in Spain: A cross-sectional study.
Ortega Suero G, Abenza Abildúa MJ, Serrano Munuera C, Rouco Axpe I, Arpa Gutiérrez FJ, Adarmes Gómez AD, Rodríguez de Rivera FJ, Quintans Castro B, Posada Rodríguez I, Vadillo Bermejo A, Domingo Santos Á, Blanco Vicente E, Infante Ceberio I, Pardo Fernández J, Costa Arpín E, Painous Martí C, Muñoz García JE, Mir Rivera P, Montón Álvarez F, Bataller Alberola L, Gascón Bayarri J, Casasnovas Pons C, Vélez Santamaría V, López de Munain A, Fernández-Eulate G, Gazulla Abío J, Sanz Gallego I, Rojas Bartolomé L, Ayo Martín Ó, Segura Martín T, González Mingot C, Baraldés Rovira M, Sivera Mascaró R, Cubo Delgado E, Echavarría Íñiguez A, Vázquez Sánchez F, Bártulos Iglesias M, Casadevall Codina MT, Martínez Fernández EM, Labandeira Guerra C, Alemany Perna B, Carvajal Hernández A, Fernández Moreno C, Palacín Larroy M, Caballol Pons N, Ávila Rivera A, Navacerrada Barrero FJ, Lobato Rodríguez R, Sobrido Gómez MJ. Ortega Suero G, et al. Among authors: rouco axpe i. Neurologia (Engl Ed). 2023 Jul-Aug;38(6):379-386. doi: 10.1016/j.nrleng.2023.04.003. Epub 2023 Apr 28. Neurologia (Engl Ed). 2023. PMID: 37120112 Free article.
Neuropsychological Profile of Hereditary Ataxias: Study of 38 Patients.
García M, Rouco-Axpe I, Amayra I, Rodríguez-Antigüedad A, Catalli C, Cabrera-Zubizarreta A, Rodríguez AA, Pérez M. García M, et al. Among authors: rouco axpe i. Arch Clin Neuropsychol. 2022 Jul 19;37(5):904-915. doi: 10.1093/arclin/acac024. Arch Clin Neuropsychol. 2022. PMID: 35484833
Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment.
Roux T, Barbier M, Papin M, Davoine CS, Sayah S, Coarelli G, Charles P, Marelli C, Parodi L, Tranchant C, Goizet C, Klebe S, Lohmann E, Van Maldergem L, van Broeckhoven C, Coutelier M, Tesson C, Stevanin G, Duyckaerts C, Brice A, Durr A; SPATAX network. Roux T, et al. Genet Med. 2020 Nov;22(11):1851-1862. doi: 10.1038/s41436-020-0899-x. Epub 2020 Jul 27. Genet Med. 2020. PMID: 32713943 Free article.
Diagnostic difficulty of a glioblastoma with an unusual presentation.
Rouco Axpe I, Mateos Goñi B, Zaldumbide Dueñas L, Fernández-Lomana Idiondo E. Rouco Axpe I, et al. Neurologia (Engl Ed). 2021 Apr;36(3):241-243. doi: 10.1016/j.nrl.2020.04.016. Epub 2020 Jun 20. Neurologia (Engl Ed). 2021. PMID: 32571555 Free article. English, Spanish. No abstract available.
Epidemiology of ataxia and hereditary spastic paraplegia in Spain: a cross-sectional study.
Ortega Suero G, Abenza Abildúa MJ, Serrano Munuera C, Rouco Axpe I, Arpa Gutiérrez FJ, Adarmes Gómez AD, Rodríguez de Rivera FJ, Quintans Castro B, Posada Rodríguez I, Vadillo Bermejo A, Domingo Santos Á, Blanco Vicente E, Infante Ceberio I, Pardo Fernández J, Costa Arpín E, Painous Martí C, Muñoz JE, Mir Rivera P, Montón Álvarez F, Bataller Alberola L, Gascón Bayarri J, Casasnovas Pons C, Vélez Santamaría V, López Munain A, Fernández García Eulate G, Gazulla Abío J, Sanz Gallego I, Rojas Bartolomé L, Ayo Martín Ó, Segura Martín T, González Mingot C, Baraldés Rovira M, Sivera Mascaró R, Cubo Delgado E, Echevarría Íñiguez A, Vázquez Sánchez F, Bártulos Iglesias M, Casadevall Codina MT, Martínez Fernández EM, Labandeira Guerra C, Alemany Perna B, Carvajal Hernández A, Fernández Moreno C, Palacín Larroy M, Caballol Pons N, Ávila Rivera A, Navacerrada Barrero FJ, Lobato Rodríguez R, Sobrido Gómez MJ. Ortega Suero G, et al. Among authors: rouco axpe i. Neurologia (Engl Ed). 2021 Mar 25:S0213-4853(21)00021-9. doi: 10.1016/j.nrl.2021.01.006. Online ahead of print. Neurologia (Engl Ed). 2021. PMID: 33775475 Free article. English, Spanish.
Hypomagnesemia: a Treatable Cause of Ataxia with Cerebellar Edema.
Rouco Axpe I, Almeida Velasco J, Barreiro Garcia JG, Urbizu Gallardo JM, Mateos Goñi B. Rouco Axpe I, et al. Cerebellum. 2017 Dec;16(5-6):988-990. doi: 10.1007/s12311-017-0873-6. Cerebellum. 2017. PMID: 28656525 No abstract available.
16 results