Claudia Nesti

6PUBLICATIONS
25CO-AUTHORS
Molecular targetsCell and nuclear divisionCardiology (incl. cardiovascular diseases)Medical biochemistry - proteins and peptides (incl. medical proteomics)Neurogenetics
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Publications (6)

|Jan 27, 2024
OPA1 mutation affects autophagy and triggers senescence in autosomal dominant optic atrophy plus fibroblasts.

Paola Zanfardino, Alessandro Amati, Stefano Doccini

|Dec 09, 2023
Novel COX11 Mutations Associated with Mitochondrial Disorder: Functional Characterization in Patient Fibroblasts and Saccharomyces cerevisiae.

Chenelle A Caron-Godon, Stefania Della Vecchia, Alessandro Romano

|May 27, 2023
Clinical, Genetic, and Histological Characterization of Patients with Rare Neuromuscular and Mitochondrial Diseases Presenting with Different Cardiomyopathy Phenotypes.

Emanuele Monda, Michele Lioncino, Martina Caiazza

|May 17, 2023
Combined Clinical, Molecular, and Muscle Biopsy Approach to Unveil Prevalence and Clinical Features of Rare Neuromuscular and Mitochondrial Diseases in Patients With Cardiomyopathies.

Michele Lioncino, Emanuele Monda, Martina Caiazza

|Mar 20, 2023
Additive effect of DNAJC30 and NDUFA9 mutations causing Leigh syndrome.

Claudia Nesti, Chiara Ticci, Anna Rubegni

|Aug 07, 2021
The Diagnostic Approach to Mitochondrial Disorders in Children in the Era of Next-Generation Sequencing: A 4-Year Cohort Study.

Deborah Tolomeo, Daniele Orsucci, Claudia Nesti

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Frequent Collaborators

4 joint publications

Filippo Maria Santorelli

3 joint publications

Giorgia Bruno

3 joint publications

Stefano Doccini

2 joint publications

Roberta Battini