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Page 1
Can Intestinal Pseudo-Obstruction Drive Recurrent Stroke-Like Episodes in Late-Onset MELAS Syndrome? A Case Report and Review of the Literature.
Gagliardi D, Mauri E, Magri F, Velardo D, Meneri M, Abati E, Brusa R, Faravelli I, Piga D, Ronchi D, Triulzi F, Peverelli L, Sciacco M, Bresolin N, Comi GP, Corti S, Govoni A. Gagliardi D, et al. Among authors: mauri e. Front Neurol. 2019 Jan 31;10:38. doi: 10.3389/fneur.2019.00038. eCollection 2019. Front Neurol. 2019. PMID: 30766507 Free PMC article.
Central Nervous System Involvement in Common Variable Immunodeficiency: A Case of Acute Unilateral Optic Neuritis in a 26-Year-Old Italian Patient.
Abati E, Faravelli I, Magri F, Govoni A, Velardo D, Gagliardi D, Mauri E, Brusa R, Bresolin N, Fabio G, Comi GP, Carrabba M, Corti S. Abati E, et al. Among authors: mauri e. Front Neurol. 2018 Nov 30;9:1031. doi: 10.3389/fneur.2018.01031. eCollection 2018. Front Neurol. 2018. PMID: 30555409 Free PMC article.
Therapeutic effect of Anakinra in the relapsing chronic phase of febrile infection-related epilepsy syndrome.
Dilena R, Mauri E, Aronica E, Bernasconi P, Bana C, Cappelletti C, Carrabba G, Ferrero S, Giorda R, Guez S, Scalia Catenacci S, Triulzi F, Barbieri S, Calderini E, Vezzani A. Dilena R, et al. Among authors: mauri e. Epilepsia Open. 2019 Mar 27;4(2):344-350. doi: 10.1002/epi4.12317. eCollection 2019 Jun. Epilepsia Open. 2019. PMID: 31168503 Free PMC article.
Ophthalmoplegia Due to Miller Fisher Syndrome in a Patient With Myasthenia Gravis.
Brusa R, Faravelli I, Gagliardi D, Magri F, Cogiamanian F, Saccomanno D, Cinnante C, Mauri E, Abati E, Bresolin N, Corti S, Comi GP. Brusa R, et al. Among authors: mauri e. Front Neurol. 2019 Aug 13;10:823. doi: 10.3389/fneur.2019.00823. eCollection 2019. Front Neurol. 2019. PMID: 31456730 Free PMC article.
Estimating the impact of COVID-19 pandemic on services provided by Italian Neuromuscular Centers: an Italian Association of Myology survey of the acute phase.
Mauri E, Abati E, Musumeci O, Rodolico C, D'Angelo MG, Mirabella M, Lucchini M, Bello L, Pegoraro E, Maggi L, Manneschi L, Gemelli C, Grandis M, Zuppa A, Massucco S, Benedetti L, Caponnetto C, Schenone A, Prelle A, Previtali SC, Scarlato M, D'Amico A, Bertini E, Pennisi EM, De Giglio L, Pane M, Mercuri E, Mongini T, Ricci F, Berardinelli A, Astrea G, Lenzi S, Battini R, Ricci G, Torri F, Siciliano G, Santorelli FM, Ariatti A, Filosto M, Passamano L, Politano L, Scutifero M, Tonin P, Fossati B, Panicucci C, Bruno C, Ravaglia S, Monforte M, Tasca G, Ricci E, Petrucci A, Santoro L, Ruggiero L, Barp A, Albamonte E, Sansone V, Gagliardi D, Costamagna G, Govoni A, Magri F, Brusa R, Velardo D, Meneri M, Sciacco M, Corti S, Bresolin N, Moroni I, Messina S, Di Muzio A, Nigro V, Liguori R, Antonini G, Toscano A, Minetti C, Comi GP; Italian Association of Myology. Mauri E, et al. Acta Myol. 2020 Jun 1;39(2):57-66. doi: 10.36185/2532-1900-008. eCollection 2020 Jun. Acta Myol. 2020. PMID: 32904925 Free PMC article.
Expanding the clinical spectrum of the mitochondrial mutation A13084T in the ND5 gene.
Brusa R, Mauri E, Dell'Arti L, Magri F, Ronchi D, Minorini V, Mainetti C, Gagliardi D, Faravelli I, Meneri M, Bresolin N, Viola F, Corti S, Comi GP. Brusa R, et al. Among authors: mauri e. Neurol Genet. 2020 Sep 15;6(5):e511. doi: 10.1212/NXG.0000000000000511. eCollection 2020 Oct. Neurol Genet. 2020. PMID: 33062892 Free PMC article. No abstract available.
91 results