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Year Number of Results
2010 1
2011 1
2013 1
2014 2
2015 2
2016 2
2017 1
2018 4
2019 5
2020 4
2021 3
2022 1
2023 5
2024 0

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31 results

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Page 1
Sex differences in ischemic stroke during COVID-19 first outbreak in northern Italy.
Sangalli D, Versino M, Colombo I, Ciccone A, Beretta S, Marcheselli S, Roncoroni M, Beretta S, Lorusso L, Cavallini A, Prelle A, Guidetti D, La Gioia S, Canella S, Zanferrari C, Grampa G, d'Adda E, Peverelli L, Colombo A, Martinelli-Boneschi F, Salmaggi A; SNO-COVID-19 group. Sangalli D, et al. Among authors: peverelli l. J Neurol Sci. 2023 Nov 15;454:120848. doi: 10.1016/j.jns.2023.120848. Epub 2023 Oct 31. J Neurol Sci. 2023. PMID: 37939626
NGS-Based Genetic Analysis in a Cohort of Italian Patients with Suspected Inherited Myopathies and/or HyperCKemia.
Invernizzi F, Izzo R, Colangelo I, Legati A, Zanetti N, Garavaglia B, Lamantea E, Peverelli L, Ardissone A, Moroni I, Maggi L, Bonanno S, Fiori L, Velardo D, Magri F, Comi GP, Ronchi D, Ghezzi D, Lamperti C. Invernizzi F, et al. Among authors: peverelli l. Genes (Basel). 2023 Jul 2;14(7):1393. doi: 10.3390/genes14071393. Genes (Basel). 2023. PMID: 37510298 Free PMC article.
Correction to: COVID‑19‑associated Guillain‑Barré syndrome in the early pandemic experience in Lombardia (Italy).
Martinelli-Boneschi F, Colombo A, Bresolin N, Sessa M, Bassi P, Grampa G, Magni E, Versino M, Ferrarese C, Zarcone D, Albanese A, Micieli G, Zanferrari C, Cagnana A, Ferrante C, Zilioli A, Locatelli D, Calloni MV, Delodovici ML, Pozzato M, Patisso V, Bortolan F, Foresti C, Frigeni B, Canella S, Xhani R, Crabbio M, Clemenzi A, Mauri M, Beretta S, La Spina I, Bernasconi S, De Santis T, Cavallini A, Ranieri M, D'Adda E, Fruguglietti ME, Peverelli L, Agosti E, Leoni O, Rigamonti A, Salmaggi A. Martinelli-Boneschi F, et al. Among authors: peverelli l. Neurol Sci. 2023 Apr;44(4):1475-1476. doi: 10.1007/s10072-022-06512-y. Neurol Sci. 2023. PMID: 36427103 Free PMC article. No abstract available.
COVID-19-associated Guillain-Barré syndrome in the early pandemic experience in Lombardia (Italy).
Martinelli-Boneschi F, Colombo A, Bresolin N, Sessa M, Bassi P, Grampa G, Magni E, Versino M, Ferrarese C, Zarcone D, Albanese A, Micieli G, Zanferrari C, Cagnana A, Ferrante C, Zilioli A, Locatelli D, Calloni MV, Delodovici ML, Pozzato M, Patisso V, Bortolan F, Foresti C, Frigeni B, Canella S, Xhani R, Crabbio M, Clemenzi A, Mauri M, Beretta S, La Spina I, Bernasconi S, De Santis T, Cavallini A, Ranieri M, D'Adda E, Fruguglietti ME, Peverelli L, Agosti E, Leoni O, Rigamonti A, Salmaggi A. Martinelli-Boneschi F, et al. Among authors: peverelli l. Neurol Sci. 2023 Feb;44(2):437-446. doi: 10.1007/s10072-022-06429-6. Epub 2022 Oct 26. Neurol Sci. 2023. PMID: 36289117 Free PMC article.
Leber's Hereditary Optic Neuropathy: A Report on Novel mtDNA Pathogenic Variants.
Peverelli L, Catania A, Marchet S, Ciasca P, Cammarata G, Melzi L, Bellino A, Fancellu R, Lamantea E, Capristo M, Caporali L, La Morgia C, Carelli V, Ghezzi D, Bianchi Marzoli S, Lamperti C. Peverelli L, et al. Front Neurol. 2021 Jun 9;12:657317. doi: 10.3389/fneur.2021.657317. eCollection 2021. Front Neurol. 2021. PMID: 34177762 Free PMC article.
Impact of SARS-CoV-2 infection on acute intracerebral haemorrhage in northern Italy.
Sangalli D, Martinelli-Boneschi F, Versino M, Colombo I, Ciccone A, Beretta S, Marcheselli S, Altavilla R, Roncoroni M, Beretta S, Lorusso L, Cavallini A, Prelle A, Guidetti D, La Gioia S, Santalucia P, Zanferrari C, Grampa G, D'Adda E, Peverelli L, Colombo A, Salmaggi A; SNO-COVID-19 group. Sangalli D, et al. Among authors: peverelli l. J Neurol Sci. 2021 Jul 15;426:117479. doi: 10.1016/j.jns.2021.117479. Epub 2021 May 5. J Neurol Sci. 2021. PMID: 34004463 Free PMC article.
Limb girdle muscular dystrophy due to LAMA2 gene mutations: new mutations expand the clinical spectrum of a still challenging diagnosis.
Magri F, Brusa R, Bello L, Peverelli L, Del Bo R, Govoni A, Cinnante C, Colombo I, Fortunato F, Tironi R, Corti S, Grimoldi N, Sciacco M, Bresolin N, Pegoraro E, Moggio M, Comi GP. Magri F, et al. Among authors: peverelli l. Acta Myol. 2020 Jun 1;39(2):67-82. doi: 10.36185/2532-1900-009. eCollection 2020 Jun. Acta Myol. 2020. PMID: 32904964 Free PMC article.
MYH2 myopathy, a new case expands the clinical and pathological spectrum of the recessive form.
Telese R, Pagliarani S, Lerario A, Ciscato P, Fagiolari G, Cassandrini D, Grimoldi N, Conte G, Cinnante C, Santorelli FM, Comi GP, Sciacco M, Peverelli L. Telese R, et al. Among authors: peverelli l. Mol Genet Genomic Med. 2020 Sep;8(9):e1320. doi: 10.1002/mgg3.1320. Epub 2020 Jun 24. Mol Genet Genomic Med. 2020. PMID: 32578970 Free PMC article.
31 results