Ronchi Dario
Professore Associato
Settore scientifico-disciplinare
MEDS-12/A - Neurologia
Gruppo scientifico-disciplinare / settore concorsuale
06/MEDS-12 - NEUROLOGIA
Competenze e ambito di ricerca
Office hours
Disponibile su richiesta
Luogo di ricevimento
via Francesco Sforza 35, Ospedale Maggiore Policlinico
Teaching - Programme courses
Bachelors and masters
A.A. 2025/2026
A.A. 2024/2025
A.A. 2023/2024
A.A. 2022/2023
A.A. 2021/2022
A.A. 2020/2021
A.A. 2018/2019
Postgraduate programmes
A.A. 2024/2025
Dottorato
A.A. 2023/2024
Dottorato
A.A. 2022/2023
Research
Publications
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Case Report: Incidental late-onset Pompe disease diagnosis in a man with no clinical and instrumental evidence of neuromuscular dysfunction / M. Sciacco, S. Lucchiari, L. Bertolasi, G.P. Comi, S. Corti, D. Ronchi. - In: FRONTIERS IN GENETICS. - ISSN 1664-8021. - 16:(2025), pp. 1574381.1-1574381.8. [10.3389/fgene.2025.1574381]
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A novel DNM2 variant associated with centronuclear myopathy: a case report / M. Rimoldi, D. Velardo, S. Zanotti, M. Ripolone, R. Del Bo, P. Ciscato, L. Napoli, S. Corti, G.P. Comi, D. Ronchi. - In: FRONTIERS IN GENETICS. - ISSN 1664-8021. - 16:(2025), pp. 1559773.1-1559773.8. [10.3389/fgene.2025.1559773]
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Case report: Multiple approach analysis in a case of clinically assessed myotonia congenita / S. Lucchiari, F. Fortunato, G. Meola, A. Mignarri, S. Pagliarani, S. Corti, G.P. Comi, D. Ronchi. - In: FRONTIERS IN GENETICS. - ISSN 1664-8021. - 15:(2024 Dec 06), pp. 1486977.1-1486977.8. [10.3389/fgene.2024.1486977]
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Guanylate Kinase 1 Deficiency: A Novel and Potentially Treatable Mitochondrial DNA Depletion/Deletions Disease / A. Hidalgo-Gutierrez, J. Shintaku, J. Ramon, E. Barriocanal-Casado, A. Pesini, R.P. Saneto, G. Garrabou, J.C. Milisenda, A. Matas-Garcia, L. Gort, O. Ugarteburu, Y. Gu, L. Koganti, T. Wang, S. Tadesse, M. Meneri, M. Sciacco, S. Wang, K. Tanji, M.S. Horwitz, M.O. Dorschner, M. Mansukhani, G.P. Comi, D. Ronchi, R. Marti, A. Ribes, F. Tort, M. Hirano. - In: ANNALS OF NEUROLOGY. - ISSN 1531-8249. - 96:6(2024 Dec), pp. 1209-1224. [10.1002/ana.27071]
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Pathogenic TNNI1 variants disrupt sarcomere contractility resulting in hypo- and hypercontractile muscle disease / S. Donkervoort, M. van de Locht, D. Ronchi, J. Reunert, C.A. Mclean, M. Zaki, R. Orbach, J.M. de Winter, S. Conijn, D. Hoomoedt, O.L.A. Neto, F. Magri, A.N. Viaene, A.R. Foley, S. Gorokhova, V. Bolduc, Y. Hu, N. Acquaye, L. Napoli, J.H. Park, K. Immadisetty, L.B. Miles, M. Essawi, S. Mcmodie, L.F. Ferreira, S. Zanotti, S.B. Neuhaus, L. Medne, N. Elbagoury, K.R. Johnson, Y. Zhang, N.G. Laing, M.R. Davis, R.J. Bryson-Richardson, D.T. Hwee, J.J. Hartman, F.I. Malik, P.M. Kekenes-Huskey, G.P. Comi, W. Sharaf-Eldin, T. Marquardt, G. Ravenscroft, C.G. Bönnemann, C.A.C. Ottenheijm. - In: SCIENCE TRANSLATIONAL MEDICINE. - ISSN 1946-6242. - 16:741(2024 Apr 03), pp. eadg2841.1-eadg2841.13. [10.1126/scitranslmed.adg2841]