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Year Number of Results
2012 2
2013 2
2016 1
2017 3
2018 1
2020 3
2021 10
2022 4
2023 3
2024 1

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Page 1
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.
Subclinical myopathic changes in COVID-19.
Villa D, Ardolino G, Borellini L, Cogiamanian F, Vergari M, Savojardo V, Peyvandi F, Barbieri S. Villa D, et al. Among authors: borellini l. Neurol Sci. 2021 Oct;42(10):3973-3979. doi: 10.1007/s10072-021-05469-8. Epub 2021 Jul 25. Neurol Sci. 2021. PMID: 34304328 Free PMC article.
Harmonizing Genetic Testing for Parkinson's Disease: Results of the PARKNET Multicentric Study.
Di Fonzo A, Percetti M, Monfrini E, Palmieri I, Albanese A, Avenali M, Bartoletti-Stella A, Blandini F, Brescia G, Calandra-Buonaura G, Campopiano R, Capellari S, Colangelo I, Comi GP, Cuconato G, Ferese R, Galandra C, Gambardella S, Garavaglia B, Gaudio A, Giardina E, Invernizzi F, Mandich P, Mineri R, Panteghini C, Reale C, Trevisan L, Zampatti S, Cortelli P, Valente EM; PARKNET study group. Di Fonzo A, et al. Mov Disord. 2023 Dec;38(12):2241-2248. doi: 10.1002/mds.29617. Epub 2023 Sep 26. Mov Disord. 2023. PMID: 37750340
A Novel Homozygous VPS11 Variant May Cause Generalized Dystonia.
Monfrini E, Cogiamanian F, Salani S, Straniero L, Fagiolari G, Garbellini M, Carsana E, Borellini L, Biella F, Moggio M, Bresolin N, Corti S, Duga S, Comi GP, Aureli M, Di Fonzo A. Monfrini E, et al. Among authors: borellini l. Ann Neurol. 2021 Apr;89(4):834-839. doi: 10.1002/ana.26021. Epub 2021 Feb 2. Ann Neurol. 2021. PMID: 33452836 Free PMC article.
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.
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
CACNA1S mutation associated with a case of juvenile-onset congenital myopathy.
Mauri E, Piga D, Pagliarani S, Magri F, Manini A, Sciacco M, Ripolone M, Napoli L, Borellini L, Cinnante C, Cassandrini D, Corti S, Bresolin N, Comi GP, Govoni A. Mauri E, et al. Among authors: borellini l. J Neurol Sci. 2021 Dec 15;431:120047. doi: 10.1016/j.jns.2021.120047. Epub 2021 Nov 3. J Neurol Sci. 2021. PMID: 34763287 No abstract available.
Peri-lead edema and local field potential correlation in post-surgery subthalamic nucleus deep brain stimulation patients.
Prenassi M, Borellini L, Bocci T, Scola E, Barbieri S, Priori A, Ferrucci R, Cogiamanian F, Locatelli M, Rampini P, Vergari M, Pastore S, Datola B, Marceglia S. Prenassi M, et al. Among authors: borellini l. Front Hum Neurosci. 2022 Sep 8;16:950434. doi: 10.3389/fnhum.2022.950434. eCollection 2022. Front Hum Neurosci. 2022. PMID: 36158622 Free PMC article.
27 results