RIGUZZI, PIETRO

RIGUZZI, PIETRO  

Università di Padova  

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Risultati 1 - 14 di 14 (tempo di esecuzione: 0.03 secondi).
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
Characterisation of a large, single-centre cohort of patients with Becker muscular dystrophy to inform standardised care guidelines 2025 Riguzzi, PietroPegoraro, ElenaBello, Luca + JOURNAL OF NEUROLOGY - -
Deep characterization of females with heterozygous Duchenne muscular dystrophy mutations 2025 Riguzzi, PietroSabbatini, DanieleFusto, AuroraVianello, SaraMerlo, BeatriceCapece, GiulianaGorgoglione, DomenicoSorarù, GianniBariani, RiccardoBauce, BarbaraMartini, MarikaBello, LucaPegoraro, Elena + JOURNAL OF NEUROLOGY - -
Evaluation of aggrephagy markers in myofibrillar myopathies 2025 Riguzzi, PietroVianello, SaraBello, LucaPegoraro, Elena + ACTA NEUROPATHOLOGICA COMMUNICATIONS - -
Longitudinal Changes of Motor Function in Becker Muscular Dystrophy 2025 Bello, LucaRiguzzi, PietroCapece, GiulianaSabbatini, DanieleGorgoglione, DomenicoVianello, SaraSorarù, GianniPegoraro, Elena + NEUROLOGY. GENETICS - -
Muscle Biopsy Findings in Valosin-Containing Protein Multisystem Proteinopathy 2025 Pegoraro, ElenaRiguzzi, Pietro + NEUROLOGY. GENETICS - -
Opinion of the Italian Association of Myology on Ataluren for the Treatment of Nonsense Mutation Duchenne Muscular Dystrophy 2025 Bello, LucaRiguzzi, PietroPegoraro, Elena + DRUGS IN R&D - -
Robotic Thymectomy for Myasthenia Gravis: Analysis of the Surgical and Neurological Outcomes After a 20 Years' Experience 2025 Comacchio, Giovanni MSchiavon, MarcoBello, LucaMammana, MarcoFaccioli, EleonoraPegoraro, ElenaLorenzoni, GiuliaCannone, GiorgioGregori, DarioCapece, GiulianaRiguzzi, PietroPezzuto, FedericaCalabrese, FiorellaDell'Amore, AndreaRea, Federico + EUROPEAN JOURNAL OF NEUROLOGY - -
Focal epilepsy followed by rapidly progressive frontotemporal dementia: a rare manifestation of VCP mutation 2024 Salvalaggio, AlessandroRiguzzi, PietroCecchin, DiegoCagnin, Annachiara + AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION - -
Natural history of Becker muscular dystrophy: DMD gene mutations predict clinical severity 2024 Gorgoglione, DomenicoSabbatini, DanieleRiguzzi, PietroCapece, GiulianaVianello, SaraBello, LucaPegoraro, Elena + BRAIN - -
The IAAM LTBP4 Haplotype is Protective Against Dystrophin-Deficient Cardiomyopathy 2024 Bello, LucaSabbatini, DanieleGorgoglione, DomenicoRiguzzi, PietroVianello, SaraPegoraro, Elena + JOURNAL OF NEUROMUSCULAR DISEASES - -
Transition and management of patients with Duchenne Muscular Dystrophy: a narrative review based on Italian experts' opinion and real-world experience 2024 Bello, LucaRiguzzi, PietroVianello, Andrea + ACTA MYOLOGICA - -
Continuitiy of care with ataluren in Duchenne Muscular Dystrophy patients with nonsense mutations after loss of ambulation. Personal experience 2023 Bello, LucaRiguzzi, PietroVianello, Andrea + ACTA MYOLOGICA - -
Encephalopathy as unique manifestation of Sjogren's syndrome: Expanding the spectrum of steroid-responsive encephalopathy 2021 Miscioscia A.Riguzzi P.Puthenparampil M.Gallo P. + RHEUMATOLOGY - -
Next-generation sequencing application to investigate skeletal muscle channelopathies in a large cohort of Italian patients 2021 Riguzzi P.Pegoraro E. + NEUROMUSCULAR DISORDERS - -