Piervito Lopriore
Pisa, 56127, Italy
Last Updated: 09/26/2026
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Found 28 publications
Evaluating a Coenzyme Q10-Based Food for Special Medical Purpose, for Mitochondrial Diseases Management: An Open-Label, Pilot Trial.
Journal: International journal of molecular sciences
Published: April 24, 2026
Diagnostic Criteria and Management of MELAS and Stroke-Like Episodes: Consensus-Based Statements.
Journal: European journal of neurology
Published: January 10, 2026
280th ENMC International Workshop: The ERN EURO-NMD mitochondrial diseases working group; diagnostic criteria and outcome measures in primary mitochondrial myopathies. Hoofddorp, the Netherlands, 22-24 November 2024.
Journal: Neuromuscular disorders : NMD
Published: March 05, 2025
Bi-allelic mutations in FASTKD5 are associated with cytochrome c oxidase deficiency and early- to late-onset Leigh syndrome.
Journal: American journal of human genetics
Published: March 04, 2025
Characterization of Factors Associated With Death in Deceased Patients With Mitochondrial Disorders: A Multicenter Cross-Sectional Survey.
Journal: Neurology
Published: January 30, 2025
Expanding the Tyrosine Kinase Domain of CSF1R? A Case Report From an Adult-Onset Leukoencephalopathy.
Journal: American journal of medical genetics. Part A
Published: January 25, 2025
An inherited mtDNA rearrangement, mimicking a single large-scale deletion, associated with MIDD and a primary cardiological phenotype.
Journal: Mitochondrion
Published: December 17, 2024
PHEMI-Phenylbutyrate in Patients With Lactic Acidosis: A Pilot, Single Arm, Phase I/II, Open-Label Trial.
Journal: Clinical therapeutics
Published: November 07, 2024
Diagnosis of hereditary ataxias: a real-world single center experience.
Journal: Journal of neurology
Published: July 29, 2024
Disease registries and rare disorders: The virtuous example of mitochondrial medicine.
Journal: Experimental neurology
Published: June 23, 2024
Last Updated: 09/26/2026