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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2020 | 2 |
2021 | 2 |
2022 | 2 |
2024 | 1 |
Search Results
5 results
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Page 1
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. Epub 2022 Aug 18.
J Neurol. 2022.
PMID: 35980466
Free PMC article.
Adult-onset mitochondrial movement disorders: a national picture from the Italian Network.
Montano V, Orsucci D, Carelli V, La Morgia C, Valentino ML, Lamperti C, Marchet S, Musumeci O, Toscano A, Primiano G, Santorelli FM, Ticci C, Filosto M, Rubegni A, Mongini T, Tonin P, Servidei S, Ceravolo R, Siciliano G, Mancuso M.
Montano V, et al.
J Neurol. 2022 Mar;269(3):1413-1421. doi: 10.1007/s00415-021-10697-1. Epub 2021 Jul 14.
J Neurol. 2022.
PMID: 34259909
Free PMC article.
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Therapeutic Approaches to Treat Mitochondrial Diseases: "One-Size-Fits-All" and "Precision Medicine" Strategies.
Bottani E, Lamperti C, Prigione A, Tiranti V, Persico N, Brunetti D.
Bottani E, et al.
Pharmaceutics. 2020 Nov 11;12(11):1083. doi: 10.3390/pharmaceutics12111083.
Pharmaceutics. 2020.
PMID: 33187380
Free PMC article.
Review.
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Catatonia as prominent feature of stroke-like episode in MELAS.
Montano V, Simoncini C, LoGerfo A, Siciliano G, Mancuso M.
Montano V, et al.
Neurol Sci. 2021 Jan;42(1):383-385. doi: 10.1007/s10072-020-04638-5. Epub 2020 Aug 6.
Neurol Sci. 2021.
PMID: 32761397
No abstract available.
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A novel MT-ATP6 variant associated with complicated ataxia in two unrelated Italian patients: case report and functional studies.
Sala D, Marchet S, Nanetti L, Legati A, Mariotti C, Lamantea E, Ghezzi D, Catania A, Lamperti C.
Sala D, et al.
Orphanet J Rare Dis. 2024 May 16;19(1):200. doi: 10.1186/s13023-024-03212-y.
Orphanet J Rare Dis. 2024.
PMID: 38755691
Free PMC article.
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