Auré K - Search Results

1

Homoplasmic mitochondrial tRNA^Pro mutation causing exercise-induced muscle swelling and fatigue.

Auré K, Fayet G, Chicherin I, Rucheton B, Filaut S, Heckel AM, Eichler J, Caillon F, Péréon Y, Entelis N, Tarassov I, Lombès A. Auré K, et al. Neurol Genet. 2020 Jul 15;6(4):e480. doi: 10.1212/NXG.0000000000000480. eCollection 2020 Aug. Neurol Genet. 2020. PMID: 32802947 Free PMC article.

2

Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation.

Auré K, Fayet G, Leroy JP, Lacène E, Romero NB, Lombès A. Auré K, et al. Brain. 2006 May;129(Pt 5):1249-59. doi: 10.1093/brain/awl061. Epub 2006 Mar 14. Brain. 2006. PMID: 16537564

3

[Mitochondrial diseases: molecular mechanisms, clinical presentations and diagnosis investigations].

Auré K, Jardel C, Lombès A. Auré K, et al. Ann Pathol. 2005 Sep;25(4):270-81. doi: 10.1016/s0242-6498(05)80131-2. Ann Pathol. 2005. PMID: 16327653 Review. French.

4

Mitochondrial targeting of recombinant RNAs modulates the level of a heteroplasmic mutation in human mitochondrial DNA associated with Kearns Sayre Syndrome.

Comte C, Tonin Y, Heckel-Mager AM, Boucheham A, Smirnov A, Auré K, Lombès A, Martin RP, Entelis N, Tarassov I. Comte C, et al. Among authors: aure k. Nucleic Acids Res. 2013 Jan 7;41(1):418-33. doi: 10.1093/nar/gks965. Epub 2012 Oct 18. Nucleic Acids Res. 2013. PMID: 23087375 Free PMC article.

5

[Pathophysiology of human mitochondrial diseases].

Lombès A, Auré K, Jardel C. Lombès A, et al. Among authors: aure k. Biol Aujourdhui. 2015;209(2):125-32. doi: 10.1051/jbio/2015014. Epub 2015 Oct 29. Biol Aujourdhui. 2015. PMID: 26514381 Review. French.

6

[Diagnostic investigations of mitochondrial diseases with neurological symptoms].

Auré K, Lombès A. Auré K, et al. Rev Neurol (Paris). 2007 Feb;163(2):254-63. doi: 10.1016/s0035-3787(07)90400-2. Rev Neurol (Paris). 2007. PMID: 17351548 Review. French.

7

Episodic weakness due to mitochondrial DNA MT-ATP6/8 mutations.

Auré K, Dubourg O, Jardel C, Clarysse L, Sternberg D, Fournier E, Laforêt P, Streichenberger N, Petiot P, Gervais-Bernard H, Vial C, Bedat-Millet AL, Drouin-Garraud V, Bouillaud F, Vandier C, Fontaine B, Lombès A. Auré K, et al. Neurology. 2013 Nov 19;81(21):1810-8. doi: 10.1212/01.wnl.0000436067.43384.0b. Epub 2013 Oct 23. Neurology. 2013. PMID: 24153443

8

Chronic progressive ophthalmoplegia with large-scale mtDNA rearrangement: can we predict progression?

Auré K, Ogier de Baulny H, Laforêt P, Jardel C, Eymard B, Lombès A. Auré K, et al. Brain. 2007 Jun;130(Pt 6):1516-24. doi: 10.1093/brain/awm067. Epub 2007 Apr 17. Brain. 2007. PMID: 17439982

9

Unsolved issues related to human mitochondrial diseases.

Lombès A, Auré K, Bellanné-Chantelot C, Gilleron M, Jardel C. Lombès A, et al. Among authors: aure k. Biochimie. 2014 May;100:171-6. doi: 10.1016/j.biochi.2013.08.012. Epub 2013 Aug 20. Biochimie. 2014. PMID: 23973280 Free article. Review.

10

Progression despite replacement of a myopathic form of coenzyme Q10 defect.

Auré K, Benoist JF, Ogier de Baulny H, Romero NB, Rigal O, Lombès A. Auré K, et al. Neurology. 2004 Aug 24;63(4):727-9. doi: 10.1212/01.wnl.0000134607.76780.b2. Neurology. 2004. PMID: 15326254

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

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

28 results

Search Page