Alessandro Prigione

19PUBLICATIONS
114CO-AUTHORS
Energy generation, conversion and storage (excl. chemical and electrical)Computational physiologyNanomaterialsMedical infection agents (incl. prions)Child and adolescent development
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Publications (19)

|May 05, 2026
Biallelic MCUR1 nonsense mutation associated with vacuolar myopathy and altered mitochondrial calcium signaling.

|Apr 20, 2026
Accelerating Leigh syndrome drug discovery through deep learning screening in brain organoids.

|Oct 28, 2025
Brain organoid models of Huntington's disease shift the focus towards neurodevelopment.

Wenqing Xu, Alessandro Prigione

|Mar 20, 2025
Natural History of Patients With Mitochondrial ATPase Deficiency Due to Pathogenic Variants of MT-ATP6 and MT-ATP8.

Sara Carli, Anna Levarlet, Daria Diodato

|Mar 15, 2025
Patients with Allan-Herndon-Dudley Syndrome (MCT8 Deficiency) Display Symptoms of Parkinsonism in Childhood and Respond to Levodopa/Carbidopa Treatment.

Nina-Maria Wilpert, Angela L Hewitt, Roser Pons

|Oct 10, 2024
Disease models of Leigh syndrome: From yeast to organoids.

Marie-Thérèse Henke, Alessandro Prigione, Markus Schuelke

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Frequent Collaborators

6 joint publications

Markus Schuelke

4 joint publications

Sebastian Diecke

3 joint publications

Janine Kirstein

3 joint publications

Erich E Wanker