Sfoglia per Autore
Aberrant splicing due to a silent nucleotide change in CCM2 gene in a family with cerebral cavernous malformation
2009 A. Tonelli, S. Lanfranconi, A. Bersano, S. Corti, M. Bassi, N. Bresolin
Inclusion body myopathy and frontotemporal dementia caused by a novel VCP mutation
2009 A. Bersano, R. Del Bo, C. Lamperti, S. Ghezzi, G. Fagiolari, F. Fortunato, E. Ballabio, M. Moggio, L. Candelise, D. Galimberti, R. Virgilio, S. Lanfranconi, Y. Torrente, M. Carpo, N. Bresolin, G.P. Comi, S. Corti
Effect of steroid treatment in cerebellar ataxia associated with anti-glutamic acid decarboxylase antibodies
2009 R. Virgilio, S.P. Corti, P. Agazzi, D. Santoro, S. Lanfranconi, L. Candelise, N. Bresolin, G.P. Comi, A. Bersano
Stem cell therapy in stroke
2009 F. Locatelli, A. Bersano, E. Ballabio, S. Lanfranconi, D. Papadimitriou, S. Strazzer, N. Bresolin, G.P. Comi, S. Corti
Transthyretin asn90 variant: amyloidogenic or non-amyloidogenic role
2009 A. Bersano, R. Del Bo, E. Ballabio, C. Cinnante, S. Lanfranconi, G.P. Comi, P. Baron, N. Bresolin, L. Candelise
Aphasic and visual aura with increased vasogenic leakage : an atypical migrainosus status
2009 S. Lanfranconi, S. Corti, A. Bersano, A. Costa, A. Prelle, M. Sciacco, N. Bresolin, I. Ghione
Guillain-Barre syndrome after rtPA therapy for acute stroke
2010 A. Bersano, D. Santoro, A. Prelle, S. Lanfranconi, M. Ranieri, C. Tadeo, N. Bresolin, P. Baron
Clinical studies in stem cells transplantation for stroke: a review
2010 A. Bersano, E. Ballabio, S. Lanfranconi, G.B. Boncoraglio, S. Corti, F. Locatelli, P. Baron, N. Bresolin, E. Parati, L. Candelise
A cortically blind patient with preserved visual imagery
2010 S. Zago, S.P. Corti, A. Bersano, P. Baron, G. Conti, E. Ballabio, S. Lanfranconi, C.M. Cinnante, A. Costa, A. Cappellari, N. Bresolin
Anti-muSK-positive myasthenia gravis in a patient with parkinsonism and cognitive impairment
2011 S. Lanfranconi, S. Corti, P. Baron, G. Conti, L. Borellini, N. Bresolin, A. Bersano
Growth factors in ischemic stroke
2011 S. Lanfranconi, F. Locatelli, S. Corti, L. Candelise, G.P. Comi, P.L. Baron, S. Strazzer, N. Bresolin, A. Bersano
Considerations on a mutation in the NOTCH3 gene sparing a cysteine residue: a rare polymorphism rather than a CADASIL variant
2012 A. Bersano, M. Ranieri, A. Ciammola, C. Cinnante, S. Lanfranconi, M.T. Dotti, L. Candelise, C. Baschirotto, I. Ghione, E. Ballabio, N. Bresolin, M.T. Bassi
Optic neuritis as isolated manifestation of leptomeningeal carcinomatosis : a case report and systematic review of ocular manifestations of neoplastic meningitis
2013 S. Lanfranconi, P. Basilico, I. Trezzi, L. Borellini, G. Franco, V. Civelli, F. Pallotti, N. Bresolin, P. Baron
A novel CCM1 mutation associated with multiple cerebral and vertebral cavernous malformations
2014 S. Lanfranconi, D. Ronchi, N. Ahmed, V. Civelli, P. Basilico, N. Bresolin, G.P. Comi, S. Corti
Neuro-psychiatric involvement in paroxysmal nocturnal hemoglobinuria (PNH)
2016 W. Barcellini, E. Scola, S. Lanfranconi, M. Grottaroli, F. Binda, B. Fattizzo, P. Bianchi, C. Boschetti, M. Buoli, C. Altamura, N. Bresolin, F. Triulzi, A. Cortelezzi
Clinical pregenetic screening for stroke monogenic diseases: results from Lombardia GENS registry
2016 A. Bersano, H.S. Markus, S. Quaglini, E. Arbustini, S. Lanfranconi, G. Micieli, G.B. Boncoraglio, F. Taroni, C. Gellera, S. Baratta, S. Penco, L. Mosca, M. Grasso, P. Carrera, M. Ferrari, C. Cereda, G. Grieco, S. Corti, D. Ronchi, M. Teresa Bassi, L. Obici, E.A. Parati, A. Pezzini, M.L. De Lodovici, E.P. Verrengia, G. Bono, F. Mazucchelli, D. Zarcone, M.V. Calloni, P. Perrone, B.M. Bordo, A. Colombo, A. Padovani, A. Cavallini, S. Beretta, C. Ferrarese, C. Motto, E. Agostoni, G. Molini, F. Sasanelli, M. Corato, S. Marcheselli, M. Sessa, G. Comi, N. Checcarelli, M. Guidotti, D. Uccellini, E. Capitani, L. Tancredi, M. Arnaboldi, B. Incorvaia, C.S. Tadeo, L. Fusi, G. Grampa, G. Merlini, N. Trobia, G.P. Comi, M. Braga, P. Vitali, P. Baron, C. Grond-Ginsbach, L. Candelise
Brain MRI Findings and Neuro-Psychiatric Involvement in Paroxysmal Nocturnal Hemoglobinuria (PNH)
2016 W. Barcellini, E. Scola, S. Lanfranconi, M. Grottaroli, F. Binda, B. Fattizzo, A. Zaninoni, G. Valcamonica, C. Boschetti, M. Buoli, A.C. Altamura, N. Bresolin, F.M. Triulzi, A. Zanella, A. Cortelezzi
Progressive encephalomyelitis with rigidity and myoclonus associated with anti-GlyR antibodies and Hodgkin's lymphoma : A case report
2017 L. Borellini, S. Lanfranconi, S. Bonato, I. Trezzi, G. Franco, L. Torretta, N. Bresolin, A.B. Di Fonzo
A Rare Cause of Juvenile Stroke: Extracranial Carotid Artery Aneurysm with Venous Complete Reconstruction of the Carotid Bifurcation
2018 M. Domanin, S. Lanfranconi, S. Romagnoli, L. Runza, F. Cortini, G.P. Comi, L. Gabrielli
Paroxysmal Nocturnal Hemoglobinuria (Pnh) : Brain Mri Ischemic Lesions in Neurologically Asymtomatic Patients
2018 W. Barcellini, E. Scola, S. Lanfranconi, M. Grottaroli, F. Binda, B. Fattizzo, A. Zaninoni, G. Valcamonica, C.M. Cinnante, C. Boschetti, M. Buoli, C.A. Altamura, N. Bresolin, F. Triulzi, A. Zanella, A. Cortelezzi
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