SALADINO, FRANCESCA
SALADINO, FRANCESCA
Universita' degli Studi di MILANO
The mitochondrial disulfide relay system protein GFER is mutated in sutosomal-tecessive myopathy with vataract and vombined respiratory-chain deficiency
2009 A.B. Di Fonzo, D. Ronchi, T. Lodi , E. Fassone, M. Tigano, C. Lamperti, S.P. Corti, A. Bordoni, F.R. Fortunato, M. Nizzardo, L. Napoli, C. Donadoni, S. Salani, F. Saladino, M. Moggio, N. Bresolin, I. Ferrero, G.P. Comi
Transplantation of neural stem cells derived from murine embryonic stem cells ameliorates spinal muscular atrophy phenotype.
2008 S. Corti, M. Nizzardo, M. Nardini, C. Donadoni, F. Fortunato, F. Saladino, N. Bresolin, G.P. Comi
Neural stem cell transplantation can ameliorate the phenotype of a mouse model of spinal muscular atrophy
2008 S.P. Corti, M. Nizzardo, M. Nardini, C. Donadoni, S. Salani, D. Ronchi, F. Saladino, A. Bordoni, F.R. Fortunato, R. Del Bo, D. Papadimitriou, F. Locatelli, G. Menozzi, S. Strazzer, N. Bresolin, G.P. Comi
Identification of multiple mitochondrial DNA large deletions in Progressive External Ophthalmoplegia (PEO) by means of ultra-massive pyrosequencing
2008 E. Rizzi, J.P. Bonnal, R. Del Bo, M. Severgnini, M. Iacono, F. Saladino, G.P. Comi, G. Debellis
Ruolo del VEGF nella neurodegenerazione e nell’invecchiamento.
2008 S. Ghezzi, R. Del Bo, M. Scarlato, C. Fenoglio, M. Nardini, D. Santoro, A. Prelle, D. Galimberti, E. Scarpini, G. Forloni, N. Bresolin, S. Corti, G.P. Comi, F. Saladino, M. Nizzardo
Transplantation of Neural Stem Cells derived from Murine Embryonic (mES) Ameliorates Spinal Muscular Atrophy Phenotype.
2008 M. Nizzardo, S. Corti, M. Nardini, C. Donadoni, F. Fortunato, F. Saladino, N. Bresolin, G.P. Comi
Novel Twinkle (PEO1) gene mutations in mendelian progressive external ophthalmoplegia
2008 R. Virgilio, D. Ronchi, G.M. Hadjigeorgiou, A. Bordoni, F. Saladino, M. Moggio, L. Adobbati, D. Kafetsouli, E. Tsironi, S. Previtali, A. Papadimitriou, N. Bresolin, G.P. Comi
Changes in neuroimmunological pattern in IVIg treated-MMN patients : a long term follow up
2007 M. Carpo, D. Saccomanno, M. Scarlato, A. Bersano, F. Saladino, S. Allaria, E. Nobile-Orazio, N. Bresolin, G.P. Comi
A novel mutation in the mitochondrial tRNA LeuCUN gene associated with a mitochondrial myopathy with respiratory impairment
2007 R. Virgilio, A. Bordoni, D. Ronchi, F. Saladino, N. Bresolin, M. Sciacco, G.P. Comi
Parkin polymorphisms and environmental exposure: Reduction of Parkinson’s Disease age of onset XVIIth
2007 I. Ghione, A. Di Fonzo, F. Saladino, R. Del Bo, N. Bresolin, G.P. Comi, M. Rango
Screening of mitochondrial myopathy with mtDNA multiple deletions and characterization of patients without mutations in known loci
2006 R. Virgilio, D. Ronchi, A. Bordoni, L. Adobbati, G.M. Hadjigeorgiou, F. Saladino, A. Papadimitriou, M. Moggio, N. Bresolin, G.P. Comi
Survival motor neuron (SMN1 and SMN2) genes copy number in multifocal motor neuropathy
2005 F. Saladino, M. Scarlato, M. Carpo, A. Bordoni, E. Nobile-Orazio, N. Bresolin, G.P. Comi
PARK2 gene variability in idiopathic Parkinson’s disease
2005 A. Di Fonzo, I. Ghione, R. Del Bo, F. Saladino, M. Rango, N. Bresolin, G.P. Comi
PARK2 gene variability in idiopathic Parkinson's disease
2005 I. Ghione, M. Rango, A. Di Fonzo, R. Del Bo, F. Saladino, N. Bresolin, G.P. Comi