LANFRANCONI, SILVIA

LANFRANCONI, SILVIA  

Universita' degli Studi di MILANO  

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Titolo Data di pubblicazione Autori Tipo File Abstract
Circulating biomarkers in familial cerebral cavernous malformation 2024 Lanfranconi, SilviaTassi, LauraLeone, RobertoBolli, NiccoloPassamonti, Francesco + Article (author) -
Safety and efficacy of propranolol for treatment of familial cerebral cavernous malformations (Treat_CCM): a randomised, open-label, blinded-endpoint, phase 2 pilot trial 2023 Lanfranconi, SilviaBertani, Giulio ADejana, ElisabettaGiacomo P ComiGiorgio ConteMarco LocatelliDario RonchiLaura Tassi + Article (author) -
Clinical, neuroradiological and genetic findings in a cohort of patients with multiple Cerebral Cavernous Malformations 2021 Lanfranconi S.Piergallini L.Ronchi D.Valcamonica G.Conte G.Marazzi E.Bertani G. A.Locatelli M.Triulzi F.Bresolin N.Comi G. P. + 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) -
Discovering the Italian phenotype of cerebral amyloid angiopathy (CAA) : the SENECA project 2020 Scelzo E.Pantoni L.Vitali P.Lanfranconi S. + Article (author) -
Safety and efficacy of rt-PA treatment for acute stroke in pseudoxanthoma elasticum : the first report 2020 Lanfranconi S.Ghione I.Valcamonica G.Corti S. P.Bresolin N. + Article (author) -
Hereditary hemorrhagic telangiectasia associated with cortical development malformation due to a start loss mutation in ENG 2020 Cinnante C.Valcamonica G.Lanfranconi S.Ghione I.Saetti M. C.Bresolin N.Comi G. P.Ronchi D. + Article (author) -
GEN-O-MA project: an Italian network studying clinical course and pathogenic pathways of moyamoya disease—study protocol and preliminary results 2019 GIOPPO, ANDREAEsposito S.PAVANELLO, MICHELACapra V.Pantoni L.BONO, GIOVANNICAPONE, FILIPPOLanfranconi S.Perrone P.FRATIANNI, ALESSIA + Article (author) -
Paroxysmal Nocturnal Hemoglobinuria (Pnh) : Brain Mri Ischemic Lesions in Neurologically Asymtomatic Patients 2018 S. LanfranconiGROTTAROLI, MARIKAB. FattizzoVALCAMONICA, GLORIAC. M. CinnanteBOSCHETTI, CLAUDIAM. BuoliN. BresolinF. TriulziA. ZanellaA. Cortelezzi + Article (author) -
A Rare Cause of Juvenile Stroke: Extracranial Carotid Artery Aneurysm with Venous Complete Reconstruction of the Carotid Bifurcation 2018 Domanin, MaurizioLanfranconi, SilviaRomagnoli, SilviaCortini, FrancescaComi, Giacomo PieroGabrielli, Livio + Article (author) -
Progressive encephalomyelitis with rigidity and myoclonus associated with anti-GlyR antibodies and Hodgkin's lymphoma : A case report 2017 Borellini, LindaLanfranconi, SilviaBonato, SaraTrezzi, IlariaFranco, GiuliaBresolin, NereoDi Fonzo, Alessio Barnaba + Article (author) -
Brain MRI Findings and Neuro-Psychiatric Involvement in Paroxysmal Nocturnal Hemoglobinuria (PNH) 2016 Silvia LanfranconiMarika GrottaroliFrancesca BindaBruno FattizzoGloria ValcamonicaMassimiliano BuoliCarlo Alfredo AltamuraNereo BresolinFabio TriulziAlberto ZanellaAgostino Cortelezzi + Article (author) -
Neuro-psychiatric involvement in paroxysmal nocturnal hemoglobinuria (PNH) 2016 S LanfranconiM GrottaroliB FattizzoM BuoliCA AltamuraN BresolinF TriulziA Cortelezzi + Article (author) -
Clinical pregenetic screening for stroke monogenic diseases: results from Lombardia GENS registry 2016 A. BersanoS. LanfranconiG.B. BoncoraglioS. CortiD. RonchiG.P. ComiP. VitaliCANDELISE, LIVIA + Article (author) -
A novel CCM1 mutation associated with multiple cerebral and vertebral cavernous malformations 2014 S. LanfranconiD. RonchiP. BasilicoN. BresolinG.P. ComiS. Corti + Article (author) -
Optic neuritis as isolated manifestation of leptomeningeal carcinomatosis : a case report and systematic review of ocular manifestations of neoplastic meningitis 2013 S. LanfranconiP. BasilicoI. TrezziL. BorelliniG. FrancoN. Bresolin + Article (author) -
Considerations on a mutation in the NOTCH3 gene sparing a cysteine residue: a rare polymorphism rather than a CADASIL variant 2012 A. BersanoM. RanieriC. CinnanteS. LanfranconiL. CandeliseI. GhioneE. BallabioN. Bresolin + Article (author) -
Anti-muSK-positive myasthenia gravis in a patient with parkinsonism and cognitive impairment 2011 S. LanfranconiS. CortiL. BorelliniN. BresolinA. Bersano + Article (author) -
Growth factors in ischemic stroke 2011 S. LanfranconiS. CortiL. CandeliseG. P. ComiN. BresolinA. Bersano + Article (author) -
Guillain-Barre syndrome after rtPA therapy for acute stroke 2010 A. BersanoD. SantoroS. LanfranconiM. RanieriN. Bresolin + Article (author) -