BRUSA, ROBERTA

BRUSA, ROBERTA  

Universita' degli Studi di MILANO  

Risultati 1 - 20 di 20 (tempo di esecuzione: 0.0 secondi).
Titolo Data di pubblicazione Autore(i) Tipo File Abstract
Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect. A Case Report and a Review of the Literature 2-ago-2018 Gagliardi, DeliaFaravelli, IreneVilla, LuisaCinnante, ClaudiaBrusa, RobertaMauri, EleonoraTresoldi, LauraMagri, FrancescaGovoni, AlessandraBresolin, NereoComi, Giacomo PCorti, Stefania + Article (author) -
Can Intestinal Pseudo-Obstruction Drive Recurrent Stroke-Like Episodes in Late-Onset MELAS Syndrome? A Case Report and Review of the Literature 31-gen-2019 Gagliardi, DeliaMauri, EleonoraMagri, FrancescaMeneri, MegiAbati, ElenaBrusa, RobertaFaravelli, IreneRonchi, DarioTriulzi, FabioPeverelli, LorenzoBresolin, NereoComi, Giacomo PietroCorti, StefaniaGovoni, Alessandra + Article (author) -
Central nervous system involvement in common variable immunodeficiency: A case of acute unilateral optic neuritis in a 26 -year-old Italian Patient 30-nov-2018 ABATI, ELENAFaravelli, IreneMagri, FrancescaGovoni, AlessandraGagliardi, DeliaMauri, EleonoraBrusa, RobertaBresolin, NereoFabio, GiovannaComi, Giacomo PietroCARRABBA, MARIA DOMENICA ROSARIACorti, Stefania + Article (author) -
Clinical features and disease course of patients with acute ischaemic stroke just before the Italian index case: Was COVID-19 already there? 1-ago-2021 Pietroboni, Anna MLanfranconi, SilviaCarandini, TizianaArighi, AndreaAbati, ElenaBrusa, RobertaCostamagna, GianlucaLazzeri, GiuliaMauri, EleonoraPozzato, MattiaValcamonica, GloriaVilla, DavideBonato, SaraComi, Giacomo PBresolin, NereoGalimberti, DanielaScarpini, Elio + Article (author) -
Early Findings in Neonatal Cases of RYR1-Related Congenital Myopathies 28-giu-2021 Mauri, EleonoraGovoni, AlessandraBrusa, RobertaPagliarani, SerenaRipolone, MichelaCinnante, ClaudiaBresolin, NereoCorti, StefaniaComi, Giacomo PMagri, Francesca + 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 1-giu-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) -
The expanding spectrum of LAMA2 gene mutations : from congenital muscular dystrophy 1A to limb girdle muscular dystrophy 2R 1-feb-2013 F. MagriR. Del BoF. FortunatoM. D’AngeloA. GovoniR. BrusaS. BrajkovicS. CortiN. BresolinG. Comi + Article (author) -
Expanding the clinical spectrum of the mitochondrial mutation A13084T in the ND5 gene 1-gen-2020 Brusa, RobertaMauri, EleonoraDell'Arti, LauraMagri, FrancescaRonchi, DarioGagliardi, DeliaFaravelli, IreneMeneri, MegiBresolin, NereoViola, FrancescoCorti, StefaniaComi, Giacomo Pietro + Article (author) -
Human induced pluripotent stem cell models for the study and treatment of Duchenne and Becker muscular dystrophies 3-mag-2019 Salani S.Magri F.Brusa R.Mauri E.Comi G. P.Bresolin N.Corti S. + Article (author) -
Hyperacute extensive spinal cord infarction and negative spine magnetic resonance imaging: a case report and review of the literature 23-ott-2020 Costamagna, GianlucaMeneri, MegiAbati, ElenaBrusa, RobertaGagliardi, DeliaMauri, EleonoraCinnante, ClaudiaBresolin, NereoComi, GiacomoCorti, StefaniaFaravelli, Irene + Article (author) -
Impact of COVID-19 on the quality of life of patients with neuromuscular disorders in the Lombardy area, Italy 1-ott-2021 Gagliardi, DeliaCostamagna, GianlucaAbati, ElenaMauri, EleonoraBrusa, RobertaAndreoli, LucaCitterio, GaiaMagri, FrancescaMeneri, MegiBresolin, NereoCorti, StefaniaComi, Giacomo Pietro + Article (author) -
ISPD mutations account for a small proportion of Italian Limb Girdle Muscular Dystrophy cases 24-set-2015 F. MagriI. ColomboR. Del BoR. BrusaM. ScarlatoD. RonchiM.G. D'AngeloS. CortiN. BresolinG.P. Comi + Article (author) -
The Italian limb girdle muscular dystrophy registry : relative frequency, clinical features, and differential diagnosis 1-gen-2017 F. MagriM.G. D'AngeloS. CortiA. GovoniR. BrusaR. Del BoD. RonchiN. BresolinG.P. Comi + Article (author) -
The Italian registry of limb girdle muscular dystrophy : natural history, genotype-phenotype correlations and outcome measures 1-ott-2014 F. MagriA. GovoniR. BrusaM.G. D’AngeloS. GandossiniR. Del BoF. FortunatoD. RonchiS. CortiN. BresolinG.P. Comi + Article (author) -
Limb girdle muscular dystrophy due to LAMA2 gene mutations: new mutations expand the clinical spectrum of a still challenging diagnosis 1-giu-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) -
A new case of limb girdle muscular dystrophy 2G in a Greek patient, founder effect and review of the literature 1-giu-2018 Brusa, RobertaMagri, FrancescaPapadimitriou, DimitraGovoni, AlessandraDel Bo, RobertoCinnante, ClaudiaCorti, StefaniaBresolin, NereoComi, Giacomo Pietro + Article (author) -
Noncoding RNAs in Duchenne and Becker muscular dystrophies: role in pathogenesis and future prognostic and therapeutic perspectives 1-gen-2020 Brusa, RobertaMagri, FrancescaBresolin, NereoComi, Giacomo PietroCorti, Stefania Article (author) -
Ophthalmoplegia due to Miller Fisher syndrome in a patient with myasthenia gravis 1-ago-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) -
Sodium Levels Predict Disability at Discharge in Guillain-Barré Syndrome: A Retrospective Cohort Study 7-set-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) -
Subclinical Leber's hereditary optic neuropathy with pediatric acute spinal cord onset: More than meets the eye 27-dic-2018 MAURI, ELEONORARonchi, DarioTriulzi, FabioGagliardi, DeliaBrusa, RobertaFaravelli, IreneBresolin, NereoMagri, FrancescaCorti, StefaniaComi, Giacomo P. + Article (author) -