Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2021 | 1 |
2023 | 2 |
2024 | 1 |
Search Results
4 results
Results by year
Filters applied: . Clear all
It looks like you are searching for an author.
Results are currently sorted by Best Match. To see the newest results first,
change the sort order to Most Recent.
Page 1
TEFM variants impair mitochondrial transcription causing childhood-onset neurological disease.
Nat Commun. 2023 Feb 23;14(1):1009. doi: 10.1038/s41467-023-36277-7.
Nat Commun. 2023.
PMID: 36823193
Free PMC article.
Primary mitochondrial myopathies in childhood.
Olimpio C, Tiet MY, Horvath R.
Olimpio C, et al.
Neuromuscul Disord. 2021 Oct;31(10):978-987. doi: 10.1016/j.nmd.2021.08.005.
Neuromuscul Disord. 2021.
PMID: 34736635
Review.
Item in Clipboard
Variants in mitochondrial disease genes are common causes of inherited peripheral neuropathies.
Ferreira T, Polavarapu K, Olimpio C, Paramonov I, Lochmüller H, Horvath R.
Ferreira T, et al. Among authors: olimpio c.
J Neurol. 2024 Mar 28. doi: 10.1007/s00415-024-12319-y. Online ahead of print.
J Neurol. 2024.
PMID: 38549004
Item in Clipboard
Case report: Mutations in DNAJC30 causing autosomal recessive Leber hereditary optic neuropathy are common amongst Eastern European individuals.
Major TC, Arany ES, Schon K, Simo M, Karcagi V, van den Ameele J, Yu Wai Man P, Chinnery PF, Olimpio C, Horvath R.
Major TC, et al. Among authors: olimpio c.
Front Neurol. 2023 Dec 1;14:1292320. doi: 10.3389/fneur.2023.1292320. eCollection 2023.
Front Neurol. 2023.
PMID: 38107630
Free PMC article.
Item in Clipboard
Cite
Cite