Maria Andrea Desbats
3PUBLICATIONS
15CO-AUTHORS
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Publications (3)
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|Feb 20, 2026
Loss of function variants in HPDL impair human cortical development via alterations of mitochondrial function.Matteo Baggiani, Maria Andrea Desbats, Valentina Naef
|Dec 10, 2025
A novel mutation in FDX2 provides insights into the pathogenesis of MEOAL mitochondrial neuromuscular disease.Davide Doni, Deborah Grifagni, Federica Cavion
|Mar 15, 2024
A yeast based assay establishes the pathogenicity of novel missense ACTA2 variants associated with aortic aneurysms.Cristina Calderan, Ugo Sorrentino, Luca Persano
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Frequent Collaborators
1 joint publications
Cristina Calderan
1 joint publications
Ugo Sorrentino
1 joint publications
Luca Persano
1 joint publications
Eva Trevisson
1 joint publications
Leonardo Salviati
1 joint publications
Davide Doni
1 joint publications
Bianca Buchignani
1 joint publications
Roberta Battini
1 joint publications
Giuseppina Covello
1 joint publications
Oliver Stehling
