Ronchi Dario
Associate Professor
Scientific-Disciplinary Sector
MEDS-12/A - Neurology
Scientific-Disciplinary Group/Competition Sector
06/MEDS-12 - NEUROLOGIA
Research fields and competencies
Office hours
Available on request
Reception office
via Francesco Sforza 35, Policlinico Hospital
Teaching - Programme courses
Bachelors and masters
A.Y. 2024/2025
A.Y. 2021/2022
A.Y. 2020/2021
A.Y. 2018/2019
Postgraduate programmes
A.Y. 2024/2025
Doctoral programme (PhD)
A.Y. 2023/2024
Doctoral programme (PhD)
A.Y. 2022/2023
Doctoral programme (PhD)
Research
Publications
-
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]
-
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]
-
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]
-
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]
-
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]