Dario Ronchi

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 9

Top Venues

Annals of clinical and translational neurology

Annals of neurology

Neurology. Genetics

European journal of human genetics : EJHG

University of Milan

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University of Milan Apr 01 2020

Italy

Associate Professor :: Dino Ferrari Centre, Neuroscience Section, Department of Pathophysiology and Transplantation (DEPT), Neurology Unity

Publications

Agustín Hidalgo-Gutiérrez, Jonathan Shintaku, Javier Ramón, Eliana Barriocanal-Casado, Alba Pesini, Russell P Saneto, Gloria Garrabou, Jose Cesar Milisenda, Ana Matas-Garcia, Laura Gort, Olatz Ugarteburu, Yue Gu, Lahari Koganti, Tian Wang, Saba Tadesse, Megi Meneri, Monica Sciacco, Shuang Wang, Kurenai Tanji, Marshall S Horwitz, Michael O Dorschner, Mahesh M Mansukhani, Giacomo Pietro Comi, Dario Ronchi, Ramon Ramon, Antonia Ribes, Frederic Tort, Michio Hirano
Guanylate Kinase 1 Deficiency: A Novel and Potentially Treatable Mitochondrial DNA Depletion/Deletions Disease. Annals of neurology (2024)
Dario Ronchi, Manuela Garbellini, Francesca Magri, Francesca Menni, Megi Meneri, Maria Francesca Bedeschi, Robertino Dilena, Valeria Cecchetti, Irene Picciolli, Francesca Furlan, Valentina Polimeni, Sabrina Salani, Laura Pezzoli, Francesco Fortunato, Matteo Bellini, Daniela Piga, Michela Ripolone, Simona Zanotti, Laura Napoli, Patrizia Ciscato, Monica Sciacco, Giovanna Mangili, Fabio Mosca, Stefania Corti, Maria Iascone, Giacomo Pietro Comi
A biallelic variant in COX18 cause isolated Complex IV deficiency associated with neonatal encephalo-cardio-myopathy and axonal sensory neuropathy. European journal of human genetics : EJHG (2023)
Martina Ricci, Gianpaolo Cicala, Anna Capasso, Giorgia Coratti, Stefania Fiori, Costanza Cutrona, Adele D'Amico, Valeria A Sansone, Claudio Bruno, Sonia Messina, Tiziana Mongini, Michela Coccia, Gabriele Siciliano, Elena Pegoraro, Riccardo Masson, Massimiliano Mirabella, Giacomo Pietro Comi, Stefania P Corti, Dario Ronchi, Lorenzo Maggi, Maria G D'Angelo, Veria Vacchiano, Chiara Ticci, Lucia Ruggiero, Lorenzo Verriello, Federica S Ricci, Angela L Berardinelli, Maria Antonietta Maioli, Matteo Garibaldi, Vincenzo Nigro, Stefano C Previtali, Maria Carmela Pera, Eduardo Tizzano, Marika Pane, Danilo Francesco Tiziano, Eugenio Mercuri, null null
Clinical phenotype of paediatric and adult patients with spinal muscular atrophy with 4 SMN2 copies: are they really all stable? Annals of neurology (2023)
Arianna Manini, Delia Gagliardi, Megi Meneri, Sara Antognozzi, Roberto Del Bo, Cesa Scaglione, Giacomo Pietro Comi, Stefania P Corti, Dario Ronchi
Analysis of HTT CAG repeat expansion in Italian patients with amyotrophic lateral sclerosis. Annals of clinical and translational neurology 9 (11) (2022)
Francesca Magri, Simona Zanotti, Sabrina Salani, Francesco Fortunato, Patrizia Ciscato, Simonetta Gerevini, Lorenzo Maggi, Monica Sciacco, Maurizio Moggio, Stefania Corti, Nereo Bresolin, Giacomo Pietro Comi, Dario Ronchi
Antisense Morpholino-Based In Vitro Correction of a Pseudoexon-Generating Variant in the SGCB Gene. International journal of molecular sciences 23 (17) (2022)
Arianna Manini, Daniele Velardo, Patrizia Ciscato, Claudia Cinnante, Maurizio Moggio, Giacomo Comi, Stefania Corti, Dario Ronchi
Expanding the Phenotypic Spectrum of Vocal Cord and Pharyngeal Weakness With Distal Myopathy due to the p.S85C MATR3 Mutation. Neurology. Genetics 8 (4) (2022)
Elena Abati, Stefania Magri, Megi Meneri, Giulia Manenti, Daniele Velardo, Francesca Balistreri, Chiara Pisciotta, Paola Saveri, Nereo Bresolin, Giacomo Pietro Comi, Dario Ronchi, Davide Pareyson, Franco Taroni, Stefania Corti
Charcot-Marie-Tooth disease type 2F associated with biallelic HSPB1 mutations. Annals of clinical and translational neurology 8 (5) (2021)
Edoardo Monfrini, Dario Ronchi, Giulia Franco, Manuela Garbellini, Letizia Straniero, Elisa Scola, Federica Arienti, Stefano Duga, Giacomo Pietro Comi, Nereo Bresolin, Alessio di Fonzo
Late-onset leukoencephalopathy in a patient with recessive EARS2 mutations. Neurology. Genetics 6 (5) (2020)
Dario Ronchi, Edoardo Monfrini, Sara Bonato, Veronica Mancinelli, Claudia Cinnante, Sabrina Salani, Andreina Bordoni, Patrizia Ciscato, Francesco Fortunato, Marianna Villa, Alessio di Fonzo, Stefania Corti, Nereo Bresolin, Giacomo Pietro Comi
Dystonia-ataxia syndrome with permanent torsional nystagmus caused by ECHS1 deficiency. Annals of clinical and translational neurology 7 (5) (2020)

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Publication Activity (10 Years)

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Dario Ronchi