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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2014 | 1 |
2015 | 1 |
2016 | 1 |
2019 | 1 |
2022 | 1 |
2024 | 0 |
PubMed for id: 331718
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DNAJC30 defect: a frequent cause of recessive Leber hereditary optic neuropathy and Leigh syndrome.
Brain. 2022 Jun 3;145(5):1624-1631. doi: 10.1093/brain/awac052.
Brain. 2022.
PMID: 35148383
Free PMC article.
Adult-onset Leigh syndrome linked to the novel stop codon mutation m.6579G>A in MT-CO1.
Poole OV, Everett CM, Gandhi S, Marino S, Bugiardini E, Woodward C, Lam A, Quinlivan R, Hanna MG, Pitceathly RDS.
Poole OV, et al.
Mitochondrion. 2019 Jul;47:294-297. doi: 10.1016/j.mito.2019.02.004. Epub 2019 Feb 8.
Mitochondrion. 2019.
PMID: 30743023
Review.
Item in Clipboard
Leigh syndrome: Resolving the clinical and genetic heterogeneity paves the way for treatment options.
Gerards M, Sallevelt SC, Smeets HJ.
Gerards M, et al.
Mol Genet Metab. 2016 Mar;117(3):300-12. doi: 10.1016/j.ymgme.2015.12.004. Epub 2015 Dec 19.
Mol Genet Metab. 2016.
PMID: 26725255
Review.
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Adult onset Leigh syndrome with mitochondrial DNA 8344 A>G mutation.
Han JY, Sung JJ, Park HK, Yoon BN, Lee KW.
Han JY, et al.
J Clin Neurosci. 2014 Nov;21(11):2009-11. doi: 10.1016/j.jocn.2014.03.020. Epub 2014 Jun 21.
J Clin Neurosci. 2014.
PMID: 24961732
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