RINCHETTI, PAOLA

RINCHETTI, PAOLA  

Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti  

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Titolo Data di pubblicazione Autori Tipo File Abstract
Brain Calcifications: Genetic, Molecular, and Clinical Aspects 2023 Monfrini E.Arienti F.Rinchetti P.Lotti F. + Article (author) -
Sumoylation regulates the assembly and activity of the SMN complex 2021 Faravelli I.Rinchetti P.Corti S. + Article (author) -
DEVELOPMENT OF 3D IN VITRO MODEL TO STUDY MOLECULAR MECHANISMS OF SPINAL MUSCULAR ATROPHY 2020 RINCHETTI, PAOLA Doctoral Thesis -
Optimization of AAV9 gene therapy for Spinal Muscular Atrophy with respiratory distress Type 1 using in vivo disease models 2020 Pagliari E.Rinchetti P.Galli N.Taiana M.Comi GP.Corti S.Nizzardo M. + Conference Object -
SETX (senataxin), the helicase mutated in AOA2 and ALS4, functions in autophagy regulation 2020 Rinchetti P. + Article (author) -
Systematic elucidation of neuron-astrocyte interaction in models of amyotrophic lateral sclerosis using multi-modal integrated bioinformatics workflow 2020 Nizzardo, MonicaPapadimitriou, DimitraRinchetti, PaolaCorti, Stefania + Article (author) -
Neurofascin (NFASC) gene mutation causes autosomal recessive ataxia with demyelinating neuropathy 2019 Monfrini, EdoardoStraniero, LetiziaBonato, SaraMonzio Compagnoni, GiacomoBordoni, AndreinaRinchetti, PaolaSilipigni, RosamariaRonchi, DarioCorti, StefaniaComi, Giacomo P.Bresolin, NereoDuga, StefanoDi Fonzo, Alessio + Article (author) -
MicroRNA Metabolism and Dysregulation in Amyotrophic Lateral Sclerosis 2017 P. RinchettiM. RizzutiI. FaravelliS. Corti Article (author) -
Peptide-conjugated Morpholino Oligomers for treatment of Spinal Muscular Atrophy 2016 A. RamirezM. RizzutiF. RizzoP. RinchettiM. BucchiaN. BresolinG. P. ComiS. CortiM. Nizzardo Conference Object -
Is spinal muscular atrophy a disease of the motor neurons only: pathogenesis and therapeutic implications? 2016 C. SimoneA. RamirezM. BucchiaP. RinchettiD. PapadimitriouS. Corti + Article (author) -
Gene therapy rescues disease phenotype in a spinal muscular atrophy with respiratory distress type 1 (SMARD1) mouse model 2015 M. NizzardoC. SimoneF. RizzoS. SalaniP. RinchettiR. Del BoS. DamettiN. BresolinG. ComiS. Corti + Conference Object -
Gene therapy rescues disease phenotype in a spinal muscular atrophy with respiratory distress type 1 (SMARD1) mouse model 2015 M. NizzardoC. SimoneF. RizzoS. SalaniS. DamettiP. RinchettiR. Del BoN. BresolinG.P. ComiS. Corti + Article (author) -
Clinical and molecular features and therapeutic perspectives of spinal muscular atrophy with respiratory distress type 1 2015 P. RinchettiF. PorroS. Corti + Article (author) -
The wide spectrum of clinical phenotypes of spinal muscular atrophy with respiratory distress type 1: a systematic review 2014 F. PorroP. RinchettiF. MagriG. RiboldiM. NizzardoC. SimoneI. FaravelliS. Corti + Article (author) -
Motor neuron derivation from human embryonic and induced pluripotent stem cells: experimental approaches and clinical perspectives 2014 I. FaravelliM. BucchiaP. RinchettiM. NizzardoC. SimoneE. FrattiniS. Corti Article (author) -