LANFRANCONI, SILVIA

LANFRANCONI, SILVIA  

Universita' degli Studi di MILANO  

Risultati 1 - 20 di 26 (tempo di esecuzione: 0.0 secondi).
Titolo Data di pubblicazione Autore(i) Tipo File Abstract
A cortically blind patient with preserved visual imagery 1-mar-2010 S. ZagoS.P. CortiA. BersanoE. BallabioS. LanfranconiC.M. CinnanteN. Bresolin + Article (author) -
Aberrant splicing due to a silent nucleotide change in CCM2 gene in a family with cerebral cavernous malformation 1-gen-2009 S. LanfranconiA. BersanoS. CortiN. Bresolin + Article (author) -
Anti-muSK-positive myasthenia gravis in a patient with parkinsonism and cognitive impairment 1-gen-2011 S. LanfranconiS. CortiL. BorelliniN. BresolinA. Bersano + Article (author) -
Aphasic and visual aura with increased vasogenic leakage : an atypical migrainosus status 15-ott-2009 S. LanfranconiS. CortiA. BersanoA. CostaN. BresolinI. Ghione + Article (author) -
Brain MRI Findings and Neuro-Psychiatric Involvement in Paroxysmal Nocturnal Hemoglobinuria (PNH) 1-gen-2016 Silvia LanfranconiMarika GrottaroliFrancesca BindaBruno FattizzoGloria ValcamonicaMassimiliano BuoliCarlo Alfredo AltamuraNereo BresolinFabio TriulziAlberto ZanellaAgostino Cortelezzi + 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) -
Clinical pregenetic screening for stroke monogenic diseases: results from Lombardia GENS registry 1-gen-2016 A. BersanoS. LanfranconiG.B. BoncoraglioS. CortiD. RonchiG.P. ComiP. VitaliCANDELISE, LIVIA + Article (author) -
Clinical studies in stem cells transplantation for stroke: a review 1-gen-2010 A. BersanoE. BallabioS. LanfranconiG.B. BoncoraglioS. CortiF. LocatelliN. BresolinL. Candelise + Article (author) -
Clinical, neuroradiological and genetic findings in a cohort of patients with multiple Cerebral Cavernous Malformations 1-ott-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) -
Considerations on a mutation in the NOTCH3 gene sparing a cysteine residue: a rare polymorphism rather than a CADASIL variant 1-ott-2012 A. BersanoM. RanieriC. CinnanteS. LanfranconiL. CandeliseI. GhioneE. BallabioN. Bresolin + Article (author) -
Discovering the Italian phenotype of cerebral amyloid angiopathy (CAA) : the SENECA project 1-ago-2020 Scelzo E.Pantoni L.Vitali P.Lanfranconi S. + Article (author) -
Effect of steroid treatment in cerebellar ataxia associated with anti-glutamic acid decarboxylase antibodies 1-gen-2009 R. VirgilioS.P. CortiD. SantoroS. LanfranconiL. CandeliseN. BresolinG.P. ComiA. Bersano + Article (author) -
GEN-O-MA project: an Italian network studying clinical course and pathogenic pathways of moyamoya disease—study protocol and preliminary results 1-mar-2019 GIOPPO, ANDREAEsposito S.PAVANELLO, MICHELACapra V.Pantoni L.BONO, GIOVANNICAPONE, FILIPPOLanfranconi S.Perrone P.FRATIANNI, ALESSIA + Article (author) -
Growth factors in ischemic stroke 1-ago-2011 S. LanfranconiS. CortiL. CandeliseG. P. ComiN. BresolinA. Bersano + Article (author) -
Guillain-Barre syndrome after rtPA therapy for acute stroke 1-gen-2010 A. BersanoD. SantoroS. LanfranconiM. RanieriN. Bresolin + Article (author) -
Hereditary hemorrhagic telangiectasia associated with cortical development malformation due to a start loss mutation in ENG 26-ago-2020 Cinnante C.Valcamonica G.Lanfranconi S.Ghione I.Saetti M. C.Bresolin N.Comi G. P.Ronchi D. + Article (author) -
Inclusion body myopathy and frontotemporal dementia caused by a novel VCP mutation 1-gen-2009 R. Del BoC. LampertiF. FortunatoE. BallabioL. CandeliseD. GalimbertiR. VirgilioS. LanfranconiY. TorrenteM. CarpoN. BresolinG.P. ComiS. Corti + Article (author) -
Neuro-psychiatric involvement in paroxysmal nocturnal hemoglobinuria (PNH) 1-gen-2016 S LanfranconiM GrottaroliB FattizzoM BuoliCA AltamuraN BresolinF TriulziA Cortelezzi + Article (author) -
A novel CCM1 mutation associated with multiple cerebral and vertebral cavernous malformations 3-ago-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 1-gen-2013 S. LanfranconiP. BasilicoI. TrezziL. BorelliniG. FrancoN. Bresolin + Article (author) -