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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1989 | 1 |
2015 | 1 |
2017 | 1 |
2022 | 1 |
2024 | 0 |
PubMed (cited) for id: 616539
4 results
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A novel TRMT5 mutation causes a complex inherited neuropathy syndrome: The role of nerve pathology in defining a demyelinating neuropathy.
Neuropathol Appl Neurobiol. 2022 Aug;48(5):e12817. doi: 10.1111/nan.12817. Epub 2022 Apr 10.
Neuropathol Appl Neurobiol. 2022.
PMID: 35342985
TRMT5 mutations are associated with features of complex hereditary spastic paraparesis.
Tarnopolsky MA, Brady L, Tetreault M; Care4Rare Canada Consortium.
Tarnopolsky MA, et al.
Neurology. 2017 Nov 21;89(21):2210-2211. doi: 10.1212/WNL.0000000000004657. Epub 2017 Oct 11.
Neurology. 2017.
PMID: 29021354
Free PMC article.
No abstract available.
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TRMT5 Mutations Cause a Defect in Post-transcriptional Modification of Mitochondrial tRNA Associated with Multiple Respiratory-Chain Deficiencies.
Powell CA, Kopajtich R, D'Souza AR, Rorbach J, Kremer LS, Husain RA, Dallabona C, Donnini C, Alston CL, Griffin H, Pyle A, Chinnery PF, Strom TM, Meitinger T, Rodenburg RJ, Schottmann G, Schuelke M, Romain N, Haller RG, Ferrero I, Haack TB, Taylor RW, Prokisch H, Minczuk M.
Powell CA, et al.
Am J Hum Genet. 2015 Aug 6;97(2):319-28. doi: 10.1016/j.ajhg.2015.06.011. Epub 2015 Jul 16.
Am J Hum Genet. 2015.
PMID: 26189817
Free PMC article.
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Exercise intolerance, lactic acidosis, and abnormal cardiopulmonary regulation in exercise associated with adult skeletal muscle cytochrome c oxidase deficiency.
Haller RG, Lewis SF, Estabrook RW, DiMauro S, Servidei S, Foster DW.
Haller RG, et al.
J Clin Invest. 1989 Jul;84(1):155-61. doi: 10.1172/JCI114135.
J Clin Invest. 1989.
PMID: 2544623
Free PMC article.
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