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BRUSA, ROBERTA

BRUSA, ROBERTA  

Universita' degli Studi di MILANO  

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Risultati 1 - 20 di 22 (tempo di esecuzione: 0.0 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
Cognitive abnormalities in Becker muscular dystrophy: a mysterious link between dystrophin deficiency and executive functions 2023 Pezzoni, LauraBrusa, RobertaMagri, FrancescaCorti, StefaniaComi, Giacomo PietroSaetti, Maria Cristina + Article (author) -
MicroRNAs as serum biomarkers in Becker muscular dystrophy 2022 Gagliardi, DeliaBrusa, RobertaDioni, LauraBresolin, NereoComi, Giacomo PietroCorti, Stefania + 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) -
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) -
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, MattiaSacchi, LucaValcamonica, GloriaVilla, DavideBonato, SaraComi, Giacomo PBresolin, NereoGalimberti, DanielaScarpini, Elio + 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) -
Noncoding RNAs in Duchenne and Becker muscular dystrophies: role in pathogenesis and future prognostic and therapeutic perspectives 2020 Brusa, RobertaMagri, FrancescaBresolin, NereoComi, Giacomo PietroCorti, Stefania 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) -
Limb girdle muscular dystrophy due to LAMA2 gene mutations: new mutations expand the clinical spectrum of a still challenging diagnosis 2020 Magri F.Brusa R.Bello L.Peverelli L.Govoni A.Cinnante C.Colombo I.Fortunato F.Corti S.Bresolin N.Comi G. P. + 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) -
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) -
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) -
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) -
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) -
A new case of limb girdle muscular dystrophy 2G in a Greek patient, founder effect and review of the literature 2018 Brusa, RobertaMagri, FrancescaPapadimitriou, DimitraGovoni, AlessandraDel Bo, RobertoCinnante, ClaudiaCorti, StefaniaBresolin, NereoComi, Giacomo Pietro + 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) -
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) -
The Italian limb girdle muscular dystrophy registry : relative frequency, clinical features, and differential diagnosis 2017 F. MagriM.G. D'AngeloS. CortiA. GovoniR. BrusaR. Del BoD. RonchiN. BresolinG.P. Comi + Article (author) -
ISPD mutations account for a small proportion of Italian Limb Girdle Muscular Dystrophy cases 2015 F. MagriI. ColomboR. Del BoR. BrusaM. ScarlatoD. RonchiM.G. D'AngeloS. CortiN. BresolinG.P. Comi + Article (author) -