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Page 1
Internal Carotid Artery Web as the Cause of Recurrent Cryptogenic Ischemic Stroke.
Antigüedad-Muñoz J, de la Riva P, Arenaza Choperena G, Muñoz Lopetegi A, Andrés Marín N, Fernández-Eulate G, Moreno Valladares M, Martínez Zabaleta M. Antigüedad-Muñoz J, et al. J Stroke Cerebrovasc Dis. 2018 May;27(5):e86-e87. doi: 10.1016/j.jstrokecerebrovasdis.2017.12.012. Epub 2018 Jan 10. J Stroke Cerebrovasc Dis. 2018. PMID: 29331613
COL4A1 Mutation as a Cause of Familial Recurrent Intracerebral Hemorrhage.
Campo-Caballero D, Rodriguez-Antigüedad J, Ekiza-Bazan J, Iruzubieta-Agudo P, Fernández-Eulate G, Muñoz-Lopetegui A, Martínez-Zabaleta M, de la Riva P, Urtasun-Ocariz M, López de Munain A, de Arce A. Campo-Caballero D, et al. J Stroke Cerebrovasc Dis. 2020 Apr;29(4):104652. doi: 10.1016/j.jstrokecerebrovasdis.2020.104652. Epub 2020 Feb 6. J Stroke Cerebrovasc Dis. 2020. PMID: 32033901
Attention to acute cerebrovascular disease in Guipúzcoa: description of the results of a reference hospital in a centralized care model.
Fernández-Eulate G, Arocena P, Muñoz-Lopetegi A, Rodriguez-Antigüedad J, Campo-Caballero D, Equiza J, Andrés N, de Arce A, Gonzalez F, Diez N, Basterrechea J, Suquia E, de la Riva P, Martinez-Zabaleta M. Fernández-Eulate G, et al. Neurologia (Engl Ed). 2022 Jun;37(5):355-361. doi: 10.1016/j.nrleng.2019.03.022. Epub 2021 Apr 29. Neurologia (Engl Ed). 2022. PMID: 35672122 Free article. Review.
Attention to acute cerebrovascular disease in Guipúzcoa: Description of the results of a reference hospital in a centralized care model.
Fernández-Eulate G, Arocena P, Muñoz-Lopetegi A, Rodriguez-Antigüedad J, Campo-Caballero D, Equiza J, Andrés N, de Arce A, Gonzalez F, Diez N, Basterrechea J, Suquia E, de la Riva P, Martinez-Zabaleta M. Fernández-Eulate G, et al. Neurologia (Engl Ed). 2022 Jun;37(5):355-361. doi: 10.1016/j.nrl.2019.03.009. Epub 2019 Apr 30. Neurologia (Engl Ed). 2022. PMID: 31053483 Free article. English, Spanish.
Cryptococcal meningoencephalitis presenting as cerebral venous thrombosis.
Equiza J, Fernandez-Eulate G, Rodriguez-Antigüedad J, Campo-Caballero D, Muñoz-Lopetegi A, Goenaga Sanchez MA, Larrea JA, de Arce Borda A. Equiza J, et al. J Neurovirol. 2020 Apr;26(2):289-291. doi: 10.1007/s13365-019-00813-3. Epub 2019 Dec 20. J Neurovirol. 2020. PMID: 31863401
Gut microbiome and serum metabolome analyses identify molecular biomarkers and altered glutamate metabolism in fibromyalgia.
Clos-Garcia M, Andrés-Marin N, Fernández-Eulate G, Abecia L, Lavín JL, van Liempd S, Cabrera D, Royo F, Valero A, Errazquin N, Vega MCG, Govillard L, Tackett MR, Tejada G, Gónzalez E, Anguita J, Bujanda L, Orcasitas AMC, Aransay AM, Maíz O, López de Munain A, Falcón-Pérez JM. Clos-Garcia M, et al. EBioMedicine. 2019 Aug;46:499-511. doi: 10.1016/j.ebiom.2019.07.031. Epub 2019 Jul 18. EBioMedicine. 2019. PMID: 31327695 Free PMC article.
Parkinsonism and spastic paraplegia type 7: Expanding the spectrum of mitochondrial Parkinsonism.
De la Casa-Fages B, Fernández-Eulate G, Gamez J, Barahona-Hernando R, Morís G, García-Barcina M, Infante J, Zulaica M, Fernández-Pelayo U, Muñoz-Oreja M, Urtasun M, Olaskoaga A, Zelaya V, Jericó I, Saez-Villaverde R, Catalina I, Sola E, Martínez-Sáez E, Pujol A, Ruiz M, Schlüter A, Spinazzola A, Muñoz-Blanco JL, Grandas F, Holt I, Álvarez V, López de Munaín A. De la Casa-Fages B, et al. Mov Disord. 2019 Oct;34(10):1547-1561. doi: 10.1002/mds.27812. Epub 2019 Aug 21. Mov Disord. 2019. PMID: 31433872
Reply to: "Mitochondrial Parkinsonism due to SPG7/Paraplegin variants with secondary mtDNA depletion".
De la Casa-Fages B, Fernández-Eulate G, Gamez J, Barahona-Hernando R, Morís G, García-Barcina M, Infante J, Zulaica M, Fernández-Pelayo U, Muñoz-Oreja M, Urtasun M, Olaskoaga A, Zelaya V, Jericó I, Saez-Villaverde R, Catalina I, Sola E, Martínez-Sáez E, Pujol A, Ruiz M, Schlüter A, Spinazzola A, Muñoz-Blanco JL, Grandas F, Holt I, Álvarez V, López de Munaín A. De la Casa-Fages B, et al. Mov Disord. 2019 Dec;34(12):1932-1933. doi: 10.1002/mds.27899. Mov Disord. 2019. PMID: 31845766 No abstract available.
A comprehensive serum lipidome profiling of amyotrophic lateral sclerosis.
FernÁndez-Eulate G, Ruiz-Sanz JI, Riancho J, ZufirÍa M, GereÑu G, FernÁndez-TorrÓn R, Poza-Aldea JJ, Ondaro J, Espinal JB, GonzÁlez-ChinchÓn G, Zulaica M, Ruiz-Larrea MB, LÓpez De Munain A, Gil-Bea FJ. FernÁndez-Eulate G, et al. Amyotroph Lateral Scler Frontotemporal Degener. 2020 May;21(3-4):252-262. doi: 10.1080/21678421.2020.1730904. Epub 2020 Feb 28. Amyotroph Lateral Scler Frontotemporal Degener. 2020. PMID: 32106710
35 results