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Piervito Lopriore

Observed names: Lopriore P, Lopriore, Piervito, P. Lopriore
Observed institutions: University of Foggia, University of Pisa, Scuola Superiore Sant'Anna, University of Cambridge, TUM Klinikum, MRC Toxicology Unit, Technical University of Munich
ORCID: 0000-0002-9789-3129
Observed ORCID: 0000-0002-9789-3129
OpenAlex ID: A5019738510
Frontotemporal Dementia, Where Do We Stand? A Narrative Review
2023 · Annibale Antonioni, Emanuela Maria Raho, et al. · International Journal of Molecular Sciences · 123
Mitochondrial Epilepsy, a Challenge for Neurologists
2022 · Piervito Lopriore, Fábio Gomes, et al. · International Journal of Molecular Sciences · 82
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Mitochondrial Ataxias: Molecular Classification and Clinical Heterogeneity
2022 · Piervito Lopriore, Valentina Ricciarini, et al. · Neurology International · 26
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Primary mitochondrial myopathy: 12-month follow-up results of an Italian cohort
2022 · V. Montano, P. Lopriore, et al. · Journal of Neurology · 22
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Pathophysiology and Management of Fatigue in Neuromuscular Diseases
2023 · Francesca Torri, Piervito Lopriore, et al. · International Journal of Molecular Sciences · 21
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Red Flags in Primary Mitochondrial Diseases: What Should We Recognize?
2023 · Federica Conti, Serena Di Martino, et al. · International Journal of Molecular Sciences · 14
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The use of digital tools in rare neurological diseases towards a new care model: a narrative review
2024 · Francesca Torri, Gabriele Vadi, et al. · Neurological Sciences · 11
TAp73 regulates ATP7A: possible implications for ageing-related diseases
2018 · Piervito Lopriore, Nazzareno Capitanio, et al. · Aging · 9
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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
2025 · Michelangelo Mancuso, Michelangelo Mancuso, et al. · Neuromuscular Disorders · 8
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Diagnosis of hereditary ataxias: a real-world single center experience
2025 · Adriana Meli, Vincenzo Montano, et al. · Journal of Neurology · 8
Primary Coenzyme Q10 Deficiency-Related Ataxias
2024 · Piervito Lopriore, Marco Vista, et al. · Journal of Clinical Medicine · 8
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Characterization of Factors Associated With Death in Deceased Patients With Mitochondrial Disorders
2025 · Alina Ivaniuk, Irina A. Anselm, et al. · Neurology · 7
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Mitochondrial Parkinsonism: A Practical Guide to Genes and Clinical Diagnosis
2024 · Piervito Lopriore, Giovanni Palermo, et al. · Movement Disorders Clinical Practice · 7
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ZSCAN4+ mouse embryonic stem cells have an oxidative and flexible metabolic profile
2020 · Annaelena Troiano, Consiglia Pacelli, et al. · EMBO Reports · 7
Deep neurological phenotyping in oculo-dento-digital syndrome
2024 · P. Lopriore, M. Vista, et al. · Neurological Sciences · 4
Current management of primary mitochondrial disorders in EU countries: the European Reference Networks survey
2023 · Michelangelo Mancuso, Piervito Lopriore, et al. · Journal of Neurology · 4
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Parkinsonism in complex neurogenetic disorders: lessons from hereditary dementias, adult-onset ataxias and spastic paraplegias
2023 · Simone Aloisio, Sara Satolli, et al. · Neurological Sciences · 4
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Diagnostic Criteria and Management of MELAS and Stroke‐Like Episodes: Consensus‐Based Statements
2026 · Michelangelo Mancuso, Marcello Bellusci, et al. · European Journal of Neurology · 3
Disease registries and rare disorders: The virtuous example of mitochondrial medicine
2024 · Daniele Orsucci, Elena Caldarazzo Ienco, et al. · Experimental Neurology · 3
Characterization of the effect of pomegranate crude extract, and its post-harvesting preservation procedures, on redox tone, cellular growth and metabolic profile of MDA-MB-231 cell line
2023 · Aristide Ferrante, Mirko Tamma, et al. · BMC Complementary Medicine and Therapies · 3
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Bi-allelic mutations in FASTKD5 are associated with cytochrome c oxidase deficiency and early- to late-onset Leigh syndrome
2025 · Hana Antonicka, Woranontee Weraarpachai, et al. · The American Journal of Human Genetics · 2
PHEMI—Phenylbutyrate in Patients With Lactic Acidosis: A Pilot, Single Arm, Phase I/II, Open–Label Trial
2025 · Silvia Marchet, Alessia Catania, et al. · Clinical Therapeutics · 2
A Multisystem Mitochondrial Disease Caused by a Novel MT-TL1 mtDNA Variant: A Case Report
2022 · Domenico Giannese, Vincenzo Montano, et al. · Journal of Neuromuscular Diseases · 2
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Clinical and Genotypic Spectrum of Twinkle-Related Disorders
2026 · Piervito Lopriore, Zeynep Ünlütürk, et al. · Neurology · 1
An inherited mtDNA rearrangement, mimicking a single large-scale deletion, associated with MIDD and a primary cardiological phenotype
2025 · Piervito Lopriore, Andrea Legati, et al. · Mitochondrion · 1
Works count: 36
Citation count: 389
H-index: 8
I10-index: 7
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