CORTI, STEFANIA PAOLA

CORTI, STEFANIA PAOLA  

Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti  

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Titolo Data di pubblicazione Autori Tipo File Abstract
Shaping the Neurovascular Unit Exploiting Human Brain Organoids 2024 Rizzuti, MafaldaBrambilla, LorenzoOttoboni, LindaMeneri, MegiRatti, AntoniaVerde, FedericoTicozzi, NicolaComi, Giacomo PietroCorti, StefaniaAbati, Elena + Article (author) -
Characterization of Skeletal Muscle Biopsy and Derived Myoblasts in a Patient Carrying Arg14del Mutation in Phospholamban Gene 2023 Ripolone, MichelaSalani, SabrinaCorti, StefaniaComi, Giacomo + Article (author) -
Onasemnogene abeparvovec in spinal muscular atrophy: predictors of efficacy and safety in naïve patients with spinal muscular atrophy and following switch from other therapies 2023 Sansone, Valeria AdaCorti, StefaniaLeone, DanielaRicci, Martina + Article (author) -
Longitudinal transcriptomic analysis of mouse sciatic nerve reveals pathways associated with age-related muscle pathology 2023 Parodi, ChiaraCorti, Stefania + Article (author) -
The Profiling of 179 miRNA Expression in Serum from Limb Girdle Muscular Dystrophy Patients and Healthy Controls 2023 Magri, FrancescaRipolone, MichelaCorti, StefaniaComi, Giacomo Pietro + Article (author) -
Case report: Clinical and molecular characterization of two siblings affected by Brody myopathy 2023 Pagliarani, SerenaCogiamanian, FilippoCorti, StefaniaComi, Giacomo PietroRonchi, Dario + Article (author) -
A biallelic variant in COX18 cause isolated Complex IV deficiency associated with neonatal encephalo-cardio-myopathy and axonal sensory neuropathy 2023 Ronchi, DarioMagri, FrancescaMeneri, MegiDilena, RobertinoPicciolli, IreneSalani, SabrinaFortunato, FrancescoMosca, FabioCorti, StefaniaComi, Giacomo Pietro + Article (author) -
Genomic and transcriptomic advances in amyotrophic lateral sclerosis 2023 Rizzuti, MafaldaScarcella, SimoneCostamagna, GianlucaOttoboni, LindaVerde, FedericoRatti, AntoniaTicozzi, NicolaComi, Giacomo PietroCorti, StefaniaGagliardi, Delia + Article (author) -
Extracellular Matrix Disorganization and Sarcolemmal Alterations in COL6-Related Myopathy Patients with New Variants of COL6 Genes 2023 Ronchi, DarioFortunato, FrancescoCorti, StefaniaComi, Giacomo Pietro + Article (author) -
Identification of Novel Biomarkers of Spinal Muscular Atrophy and Therapeutic Response by Proteomic and Metabolomic Profiling of Human Biological Fluid Samples 2023 Meneri, MegiAbati, ElenaGagliardi, DeliaRatti, AntoniaVerde, FedericoTicozzi, NicolaComi, Giacomo P.Ottoboni, LindaCorti, Stefania + Article (author) -
Combined RNA interference and gene replacement therapy targeting MFN2 as proof of principle for the treatment of Charcot-Marie-Tooth type 2A 2023 Ottoboni, LindaAbati, ElenaTaiana, MichelaLonati, CaterinaComi, GiacomoCorti, Stefania + Article (author) -
Multi-omics profiling of CSF from spinal muscular atrophy type 3 patients after nusinersen treatment: a 2-year follow-up multicenter retrospective study 2023 Faravelli, IreneGagliardi, DeliaAbati, ElenaMeneri, MegiMagri, FrancescaParente, ValeriaRicci, GiuliaGarrone, GiuliaFontana, ManuelaCaruso, DonatellaComi, Giacomo PietroGovoni, AlessandraCorti, StefaniaOttoboni, Linda + Article (author) -
Lafora Disease: A Case Report and Evolving Treatment Advancements 2023 Ferrari Aggradi, Carola RitaRomagnoli, GloriaComi, Giacomo PietroRonchi, DarioCorti, Stefania + Article (author) -
Unraveling the Neurological Complexity of Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal Protein, and Skin Changes Syndrome: A Report of a Challenging Case of a Young Woman and Cutting-Edge Advancements in the Field 2023 Furciniti, GiocondaLo Russo, Francesco MBolli, NiccolòMeneri, MegiComi, Giacomo PCorti, Stefania P + Article (author) -
NOTCH2NLC GGC repeats are not expanded in Italian amyotrophic lateral sclerosis patients 2023 Manini, AriannaGagliardi, DeliaMeneri, MegiDel Bo, RobertoComi, Giacomo PietroCorti, StefaniaRonchi, Dario + Article (author) -
Advancing Stroke Research on Cerebral Thrombi with Omic Technologies 2023 Costamagna, GianlucaBonato, SaraCorti, StefaniaMeneri, Megi Article (author) -
Prominent muscle involvement in a familial form of mitochondrial disease due to a COA8 variant 2023 Magri, FrancescaRipolone, MichelaSalani, SabrinaFortunato, FrancescoCorti, StefaniaComi, Giacomo PietroRonchi, Dario + Article (author) -
Cognitive abnormalities in Becker muscular dystrophy: a mysterious link between dystrophin deficiency and executive functions 2023 Pezzoni, LauraBrusa, RobertaMagri, FrancescaCorti, StefaniaComi, Giacomo PietroSaetti, Maria Cristina + Article (author) -
Clinical Phenotype of Pediatric and Adult Patients With Spinal Muscular Atrophy With Four SMN2 Copies: Are They Really All Stable? 2023 Sansone, Valeria AComi, Giacomo PCorti, StefaniaRonchi, Dario + Article (author) -
Regional spreading pattern is associated with clinical phenotype in amyotrophic lateral sclerosis 2023 Maranzano, AlessioVerde, FedericoColombo, EleonoraPoletti, BarbaraDoretti, AlbertoBonetti, RuggeroGagliardi, DeliaMeneri, MegiCorti, StefaniaMorelli, ClaudiaSilani, VincenzoTicozzi, Nicola + Article (author) -