COMI, GIACOMO PIETRO

COMI, GIACOMO PIETRO  

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) -
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) -
Genomic and transcriptomic advances in amyotrophic lateral sclerosis 2023 Rizzuti, MafaldaScarcella, SimoneCostamagna, GianlucaOttoboni, LindaVerde, FedericoRatti, AntoniaTicozzi, NicolaComi, Giacomo PietroCorti, StefaniaGagliardi, Delia + 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) -
MERRF Mutation A8344G in a Four-Generation Family without Central Nervous System Involvement: Clinical and Molecular Characterization 2023 Ripolone, MichelaRonchi, DarioComi, Giacomo Pietro + Article (author) -
Tremulous spastic ataxia in a patient with a homozygous truncating SYNE1 variant 2023 Monfrini, EdoardoDe Marco, PaoloComi, Giacomo P + 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) -
Givinostat for Becker muscular dystrophy: A randomized, placebo-controlled, double-blind study 2023 Comi, Giacomo PMagri, Francesca + Article (author) -
Using Cluster Analysis to Overcome the Limits of Traditional Phenotype-Genotype Correlations: The Example of RYR1-Related Myopathies 2023 Comi, Giacomo PietroMagri, Francesca + Article (author) -
Telemedicine for cognitive impairment: a telephone survey of patients' experiences with neurological video consultation 2023 Ferrucci, RobertaPoletti, BarbaraSilani, VincenzoComi, GiacomoScarpini, Elio + 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) -
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) -
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) -
Whole-Exome Sequencing Study of Fibroblasts Derived From Patients With Cerebellar Ataxia Referred to Investigate CoQ10 Deficiency 2023 Monfrini, EdoardoBiella, FabioBrescia, GloriaComi, Giacomo P + Article (author) -
Safety and efficacy of propranolol for treatment of familial cerebral cavernous malformations (Treat_CCM): a randomised, open-label, blinded-endpoint, phase 2 pilot trial 2023 Lanfranconi, SilviaBertani, Giulio ADejana, ElisabettaGiacomo P ComiGiorgio ConteMarco LocatelliDario RonchiLaura Tassi + Article (author) -
Locus for severity implicates CNS resilience in progression of multiple sclerosis 2023 Comi G.Esposito F.Gasperi C.Islam T.Martinelli Boneschi F.Santaniello A. + 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) -
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) -
Lafora Disease: A Case Report and Evolving Treatment Advancements 2023 Ferrari Aggradi, Carola RitaRomagnoli, GloriaComi, Giacomo PietroRonchi, DarioCorti, Stefania + 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) -