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Ph.D. students

Centro di Ricerca Interdisciplinare Health Science

Piervito Lopriore

Bio

  • Resident Neurologist, University of Pisa and Azienda Ospedaliero Universitaria Pisana
  • PhD Student in Translational Medicine, Scuola Superiore Sant'Anna
  • Fellow of the European Board of Neurology

Research

  • Neurogenetics
  • Mitochondrial diseases

Publications

most relevant

  1. Lopriore P, Capitanio N, Panatta E, Di Daniele N, Gambacurta A, Melino G, Amelio I. TAp73 regulates ATP7A: possible implications for ageing-related diseases. Aging (Albany NY). 2018 Dec 8;10(12):3745-3760. doi: 10.18632/aging.101669.
  2. Troiano A, Pacelli C, Ruggieri V, Scrima R, Addeo M, Agriesti F, Lucci V, Cavaliere G, Mollica MP, Caterino M, Ruoppolo M, Paladino S, Sarnataro D, Visconte F, Tucci F, Lopriore P, Calabrò V, Capitanio N, Piccoli C, Falco G. ZSCAN4+ mouse embryonic stem cells have an oxidative and flexible metabolic profile. EMBO Rep. 2020 Jun 4;21(6):e48942. doi: 10.15252/embr.201948942.
  3. Montano V, Lopriore P, Gruosso F, Carelli V, Comi GP, Filosto M, Lamperti C, Mongini T, Musumeci O, Servidei S, Tonin P, Toscano A, Primiano G, Valentino ML, Bortolani S, Marchet S, Ricci G, Modenese A, Cotti Piccinelli S, Risi B, Meneri M, Arena IG, Siciliano G, Mancuso M. Primary mitochondrial myopathy: 12-month follow-up results of an Italian cohort. J Neurol. 2022 Dec;269(12):6555-6565. doi: 10.1007/s00415-022-11324-3.
  4. Lopriore P, Gomes F, Montano V, Siciliano G, Mancuso M. Mitochondrial Epilepsy, a Challenge for Neurologists. Int J Mol Sci. 2022 Oct 30;23(21):13216. doi: 10.3390/ijms232113216.
  5. Aloisio S, Satolli S, Bellini G, Lopriore P. Parkinsonism in complex neurogenetic disorders: lessons from hereditary dementias, adult-onset ataxias and spastic paraplegias. Neurol Sci. 2023 Oct;44(10):3379-3388. doi: 10.1007/s10072-023-07044-9.
  6. Lopriore P, Vista M, Maritato P, Caldarazzo Ienco E, Bassani L, Natale G, Tessa A, Santorelli FM, Orsucci D. Deep neurological phenotyping in oculo-dento-digital syndrome. Neurol Sci. 2024 Jun;45(6):2853-2857. doi: 10.1007/s10072-024-07331-z.
  7. Mancuso M, Lopriore P, Lamperti C, Klopstock T, Rahman S, Licchetta L, Kornblum C, Wortmann SB, Dollfus H, Papadopoulou MT, Arzimanoglou A, Scarpa M, Graessner H, Evangelista T. Current management of primary mitochondrial disorders in EU countries: the European Reference Networks survey. J Neurol. 2024 Feb;271(2):835-840. doi: 10.1007/s00415-023-12017-1.
  8. Lopriore P, Vista M, Tessa A, Giuntini M, Caldarazzo Ienco E, Mancuso M, Siciliano G, Santorelli FM, Orsucci D. Primary Coenzyme Q10 Deficiency-Related Ataxias. J Clin Med. 2024 Apr 19;13(8):2391. doi: 10.3390/jcm13082391.
  9. Lopriore P, Palermo G, Meli A, Bellini G, Benevento E, Montano V, Siciliano G, Mancuso M, Ceravolo R. Mitochondrial Parkinsonism: A Practical Guide to Genes and Clinical Diagnosis. Mov Disord Clin Pract. 2024 Aug;11(8):948-965. doi: 10.1002/mdc3.14148.
  10. Meli A, Montano V, Palermo G, Fogli A, Rocchi A, Gerfo AL, Maltomini R, Cori L, Siniscalchi A, Bernardini C, Cecchi G, Siciliano G, Ceravolo R, Caligo MA, Mancuso M, Lopriore P. Diagnosis of hereditary ataxias: a real-world single center experience. J Neurol. 2025 Jan 15;272(2):111. doi: 10.1007/s00415-024-12772-9.
  11. Ivaniuk A, Anselm IA, Bowen A, Cohen BH, Eminoglu FT, Estrella J, Gallagher RC, Ganetzky RD, Gannon J, Gorman GS, Greene C, Gropman AL, Haas RH, Hirano M, Kapoor S, Karaa A, Koenig MK, Kornblum C, Kose E, Larson A, Lichter-Konecki U, Lopriore P, Mancuso M, McFarland R, Moe AM, Morava E, Ng YS, Saneto RP, Scaglia F, Sue CM, Tarnopolsky M, Walker MA, Parikh S; as the Hong Kong Mitochondrial Diseases Interest Group. Characterization of Factors Associated With Death in Deceased Patients With Mitochondrial Disorders: A Multicenter Cross-Sectional Survey. Neurology. 2025 Feb 25;104(4):e209779. doi: 10.1212/WNL.0000000000209779.
  12. Lopriore P, Migaleddu G, Tsai PC, Fogli A, Caligo MA, Siciliano G, Cosottini M, Lee YC, Liao YC, Mancuso M, Ceravolo R, Frosini D. Expanding the Tyrosine Kinase Domain of CSF1R? A Case Report From an Adult-Onset Leukoencephalopathy. Am J Med Genet A. 2025 Mar 26:e64065. doi: 10.1002/ajmg.a.64065.
  13. Lopriore P, Legati A, Neuhofer CM, Lo Gerfo A, Kopajtich R, Barresi M, Cecchi G, Pavlov M, Izzo R, Montano V, Caligo MA, Berutti R, Mancuso M, Prokisch H, Ghezzi D. An inherited mtDNA rearrangement, mimicking a single large-scale deletion, associated with MIDD and a primary cardiological phenotype. Mitochondrion. 2025 Mar 29;83:102037. doi: 10.1016/j.mito.2025.102037.