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Page 1
Demographic and geographic vascular risk factor differences in European young adults with ischemic stroke: the 15 cities young stroke study.
Putaala J, Yesilot N, Waje-Andreassen U, Pitkäniemi J, Vassilopoulou S, Nardi K, Odier C, Hofgart G, Engelter S, Burow A, Mihalka L, Kloss M, Ferrari J, Lemmens R, Coban O, Haapaniemi E, Maaijwee N, Rutten-Jacobs L, Bersano A, Cereda C, Baron P, Borellini L, Valcarenghi C, Thomassen L, Grau AJ, Palm F, Urbanek C, Tuncay R, Durukan-Tolvanen A, van Dijk EJ, de Leeuw FE, Thijs V, Greisenegger S, Vemmos K, Lichy C, Bereczki D, Csiba L, Michel P, Leys D, Spengos K, Naess H, Bahar SZ, Tatlisumak T. Putaala J, et al. Among authors: borellini l. Stroke. 2012 Oct;43(10):2624-30. doi: 10.1161/STROKEAHA.112.662866. Epub 2012 Jul 12. Stroke. 2012. PMID: 22798330
Etiology of first-ever ischaemic stroke in European young adults: the 15 cities young stroke study.
Yesilot Barlas N, Putaala J, Waje-Andreassen U, Vassilopoulou S, Nardi K, Odier C, Hofgart G, Engelter S, Burow A, Mihalka L, Kloss M, Ferrari J, Lemmens R, Coban O, Haapaniemi E, Maaijwee N, Rutten-Jacobs L, Bersano A, Cereda C, Baron P, Borellini L, Valcarenghi C, Thomassen L, Grau AJ, Palm F, Urbanek C, Tuncay R, Durukan Tolvanen A, van Dijk EJ, de Leeuw FE, Thijs V, Greisenegger S, Vemmos K, Lichy C, Bereczki D, Csiba L, Michel P, Leys D, Spengos K, Naess H, Tatlisumak T, Bahar SZ. Yesilot Barlas N, et al. Among authors: borellini l. Eur J Neurol. 2013 Nov;20(11):1431-9. doi: 10.1111/ene.12228. Epub 2013 Jul 10. Eur J Neurol. 2013. PMID: 23837733
Molecular basis of young ischemic stroke.
Bersano A, Borellini L, Motto C, Lanfranconi S, Pezzini A, Basilico P, Micieli G, Padovani A, Parati E, Candelise L. Bersano A, et al. Among authors: borellini l. Curr Med Chem. 2013;20(31):3818-39. doi: 10.2174/09298673113209990188. Curr Med Chem. 2013. PMID: 23895686 Review.
Genetics of cerebral hemorrhage and microbleeds.
Lanfranconi S, Franco G, Borellini L, Denaro F, Basilico P, Parati E, Micieli G, Bersano A. Lanfranconi S, et al. Among authors: borellini l. Panminerva Med. 2013 Mar;55(1):11-28. Panminerva Med. 2013. PMID: 23474661 Review.
A novel homozygous PLA2G6 mutation causes dystonia-parkinsonism.
Malaguti MC, Melzi V, Di Giacopo R, Monfrini E, Di Biase E, Franco G, Borellini L, Trezzi I, Monzio Compagnoni G, Fortis P, Feraco P, Orrico D, Cucurachi L, Donner D, Rizzuti M, Ronchi D, Bonato S, Bresolin N, Corti S, Comi GP, Di Fonzo A. Malaguti MC, et al. Among authors: borellini l. Parkinsonism Relat Disord. 2015 Mar;21(3):337-9. doi: 10.1016/j.parkreldis.2015.01.001. Epub 2015 Jan 10. Parkinsonism Relat Disord. 2015. PMID: 25601130 No abstract available.
Mutational analysis of COQ2 in patients with MSA in Italy.
Ronchi D, Di Biase E, Franco G, Melzi V, Del Sorbo F, Elia A, Barzaghi C, Garavaglia B, Bergamini C, Fato R, Mora G, Del Bo R, Fortunato F, Borellini L, Trezzi I, Compagnoni GM, Monfrini E, Frattini E, Bonato S, Cogiamanian F, Ardolino G, Priori A, Bresolin N, Corti S, Comi GP, Di Fonzo A. Ronchi D, et al. Among authors: borellini l. Neurobiol Aging. 2016 Sep;45:213.e1-213.e2. doi: 10.1016/j.neurobiolaging.2016.05.022. Epub 2016 Jun 7. Neurobiol Aging. 2016. PMID: 27394078
Mutations in TMEM230 are rare in autosomal dominant Parkinson's disease.
Buongarzone G, Monfrini E, Franco G, Trezzi I, Borellini L, Frattini E, Melzi V, Di Caprio AC, Ronchi D, Monzio Compagnoni G, Cogiamanian F, Ardolino G, Bresolin N, Comi GP, Corti S, Di Fonzo A. Buongarzone G, et al. Among authors: borellini l. Parkinsonism Relat Disord. 2017 Jun;39:87-88. doi: 10.1016/j.parkreldis.2017.03.007. Epub 2017 Mar 9. Parkinsonism Relat Disord. 2017. PMID: 28318986 Free article. No abstract available.
35 results