MAURI, ELEONORA

MAURI, ELEONORA  

Universita' degli Studi di MILANO  

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Risultati 1 - 16 di 16 (tempo di esecuzione: 0.003 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
Missense mutations in small muscle protein X-linked (SMPX) cause distal myopathy with protein inclusions 2021 Magri F.Mauri E.Comi G. P. + Article (author) -
Sodium Levels Predict Disability at Discharge in Guillain-Barré Syndrome: A Retrospective Cohort Study 2021 Gagliardi D.Faravelli I.Podesta M. A.Brusa R.Mauri E.Bonato S.Scarpini E.Bresolin N.Comi G. P.Corti S. + Article (author) -
Clinical features and disease course of patients with acute ischaemic stroke just before the Italian index case: Was COVID-19 already there? 2021 Pietroboni, Anna MLanfranconi, SilviaCarandini, TizianaArighi, AndreaAbati, ElenaBrusa, RobertaCostamagna, GianlucaLazzeri, GiuliaMauri, EleonoraPozzato, MattiaValcamonica, GloriaVilla, DavideBonato, SaraComi, Giacomo PBresolin, NereoGalimberti, DanielaScarpini, Elio + Article (author) -
CACNA1S mutation associated with a case of juvenile-onset congenital myopathy 2021 Mauri E.Pagliarani S.Magri F.Manini A.Ripolone M.Borellini L.Cinnante C.Corti S.Bresolin N.Comi G. P. + Article (author) -
Early Findings in Neonatal Cases of RYR1-Related Congenital Myopathies 2021 Mauri, EleonoraGovoni, AlessandraBrusa, RobertaPagliarani, SerenaRipolone, MichelaCinnante, ClaudiaBresolin, NereoCorti, StefaniaComi, Giacomo PMagri, Francesca + Article (author) -
Impact of COVID-19 on the quality of life of patients with neuromuscular disorders in the Lombardy area, Italy 2021 Gagliardi, DeliaCostamagna, GianlucaAbati, ElenaMauri, EleonoraBrusa, RobertaAndreoli, LucaCitterio, GaiaMagri, FrancescaMeneri, MegiBresolin, NereoCorti, StefaniaComi, Giacomo Pietro + Article (author) -
Hyperacute extensive spinal cord infarction and negative spine magnetic resonance imaging: a case report and review of the literature 2020 Costamagna, GianlucaMeneri, MegiAbati, ElenaBrusa, RobertaGagliardi, DeliaMauri, EleonoraCinnante, ClaudiaBresolin, NereoComi, GiacomoCorti, StefaniaFaravelli, Irene + Article (author) -
Expanding the clinical spectrum of the mitochondrial mutation A13084T in the ND5 gene 2020 Brusa, RobertaMauri, EleonoraDell'Arti, LauraMagri, FrancescaRonchi, DarioGagliardi, DeliaFaravelli, IreneMeneri, MegiBresolin, NereoViola, FrancescoCorti, StefaniaComi, Giacomo Pietro + Article (author) -
Estimating the impact of COVID-19 pandemic on services provided by Italian Neuromuscular Centers: an Italian Association of Myology survey of the acute phase 2020 Mauri E.Abati E.D'Angelo M. G.Lucchini M.Bello L.Benedetti L.Scarlato M.Bertini E.Politano L.Scutifero M.Fossati B.Sansone V.Gagliardi D.Costamagna G.Govoni A.Magri F.Brusa R.Meneri M.Corti S.Bresolin N.Nigro V.Antonini G.Comi G. P. + Article (author) -
Can Intestinal Pseudo-Obstruction Drive Recurrent Stroke-Like Episodes in Late-Onset MELAS Syndrome? A Case Report and Review of the Literature 2019 Gagliardi, DeliaMauri, EleonoraMagri, FrancescaMeneri, MegiAbati, ElenaBrusa, RobertaFaravelli, IreneRonchi, DarioTriulzi, FabioPeverelli, LorenzoBresolin, NereoComi, Giacomo PietroCorti, StefaniaGovoni, Alessandra + Article (author) -
Human induced pluripotent stem cell models for the study and treatment of Duchenne and Becker muscular dystrophies 2019 Salani S.Magri F.Brusa R.Mauri E.Comi G. P.Bresolin N.Corti S. + Article (author) -
Ophthalmoplegia due to Miller Fisher syndrome in a patient with myasthenia gravis 2019 Brusa R.Faravelli I.Gagliardi D.Magri F.Cogiamanian F.Cinnante C.Mauri E.Abati E.Bresolin N.Corti S.Comi G. P. + Article (author) -
Acute flaccid paralysis due to Echovirus 30 in an immunosuppressed transplant recipient 2019 E. MauriL. PellegrinelliE. ParianiS. BindaF. TriulziC. BanaG. MontiniR. Dilena + Article (author) -
Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect. A Case Report and a Review of the Literature 2018 Gagliardi, DeliaFaravelli, IreneVilla, LuisaCinnante, ClaudiaBrusa, RobertaMauri, EleonoraTresoldi, LauraMagri, FrancescaGovoni, AlessandraBresolin, NereoComi, Giacomo PCorti, Stefania + Article (author) -
Subclinical Leber's hereditary optic neuropathy with pediatric acute spinal cord onset: More than meets the eye 2018 MAURI, ELEONORARonchi, DarioTriulzi, FabioGagliardi, DeliaBrusa, RobertaFaravelli, IreneBresolin, NereoMagri, FrancescaCorti, StefaniaComi, Giacomo P. + Article (author) -
Central nervous system involvement in common variable immunodeficiency: A case of acute unilateral optic neuritis in a 26 -year-old Italian Patient 2018 ABATI, ELENAFaravelli, IreneMagri, FrancescaGovoni, AlessandraGagliardi, DeliaMauri, EleonoraBrusa, RobertaBresolin, NereoFabio, GiovannaComi, Giacomo PietroCARRABBA, MARIA DOMENICA ROSARIACorti, Stefania + Article (author) -