SALADINO, FRANCESCA

SALADINO, FRANCESCA  

Universita' degli Studi di MILANO  

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Titolo Data di pubblicazione Autori Tipo File Abstract
The mitochondrial disulfide relay system protein GFER is mutated in sutosomal-tecessive myopathy with vataract and vombined respiratory-chain deficiency 2009 D. RonchiE. FassoneC. LampertiS.P. CortiA. BordoniF.R. FortunatoM. NizzardoS. SalaniF. SaladinoN. BresolinG.P. Comi + Article (author) -
Transplantation of neural stem cells derived from murine embryonic stem cells ameliorates spinal muscular atrophy phenotype. 2008 S. CortiM. NizzardoF. FortunatoF. SaladinoN. BresolinG.P. Comi + Article (author) -
Identification of multiple mitochondrial DNA large deletions in Progressive External Ophthalmoplegia (PEO) by means of ultra-massive pyrosequencing 2008 R. Del BoF. SaladinoG. P. Comi + Conference Object -
Ruolo del VEGF nella neurodegenerazione e nell’invecchiamento. 2008 R. Del BoE. ScarpiniN. BresolinS. CortiG.P. ComiF. SaladinoM. Nizzardo + Conference Object -
Transplantation of Neural Stem Cells derived from Murine Embryonic (mES) Ameliorates Spinal Muscular Atrophy Phenotype. 2008 M. NizzardoS. CortiF. SaladinoN. BresolinG.P. Comi. + Conference Object -
Novel Twinkle (PEO1) gene mutations in mendelian progressive external ophthalmoplegia 2008 R. VirgilioD. RonchiA. BordoniF. SaladinoN. BresolinG.P. Comi + Article (author) -
Neural stem cell transplantation can ameliorate the phenotype of a mouse model of spinal muscular atrophy 2008 S.P. CortiM. NizzardoM. NardiniS. SalaniD. RonchiF. SaladinoA. BordoniF.R. FortunatoR. Del BoD. PapadimitriouN. BresolinG.P. Comi + Article (author) -
A novel mutation in the mitochondrial tRNA LeuCUN gene associated with a mitochondrial myopathy with respiratory impairment 2007 R. VirgilioA. BordoniD. RonchiF. SaladinoN. BresolinG.P. Comi + Article (author) -
Changes in neuroimmunological pattern in IVIg treated-MMN patients : a long term follow up 2007 M. CarpoM. ScarlatoA. BersanoF. SaladinoE. Nobile-OrazioN. BresolinG.P. Comi + Conference Object -
Parkin polymorphisms and environmental exposure: Reduction of Parkinson’s Disease age of onset XVIIth 2007 I. GhioneA. Di FonzoF. SaladinoR. Del BoN. BresolinG.P. ComiM. Rango Conference Object -
Screening of mitochondrial myopathy with mtDNA multiple deletions and characterization of patients without mutations in known loci 2006 R. VirgilioD. RonchiA. BordoniF. SaladinoA. PapadimitriouN. BresolinG.P. Comi + Article (author) -
Survival motor neuron (SMN1 and SMN2) genes copy number in multifocal motor neuropathy 2005 F.SaladinoM. CarpoA. BordoniE. Nobile-OrazioN. BresolinG.P.Comi + Article (author) -
PARK2 gene variability in idiopathic Parkinson's disease 2005 I. GhioneA. Di FonzoR. Del BoF. SaladinoN. BresolinG.P. Comi + Article (author) -
PARK2 gene variability in idiopathic Parkinson’s disease 2005 A. Di FonzoI. GhioneR. Del BoF. SaladinoM. RangoN. BresolinG.P. Comi Article (author) -