Davis RL - Search Results

1

Generation of the iPSC line FINi002-A from a male Parkinson's disease patient carrying compound heterozygous mutations in the PRKN gene.

Pavan C, Jin J, Jong S, Strbenac D, Davis RL, Sue CM, Johnston J, Lynch T, Halliday G, Kirik D, Parish CL, Thompson LH, Ovchinnikov DA. Pavan C, et al. Among authors: davis rl. Stem Cell Res. 2023 Dec;73:103211. doi: 10.1016/j.scr.2023.103211. Epub 2023 Oct 17. Stem Cell Res. 2023. PMID: 37890334 Free article.

2

The genetics of mitochondrial disease.

Davis RL, Sue CM. Davis RL, et al. Semin Neurol. 2011 Nov;31(5):519-30. doi: 10.1055/s-0031-1299790. Epub 2012 Jan 21. Semin Neurol. 2011. PMID: 22266889 Review.

3

POLG mutations in Australian patients with mitochondrial disease.

Woodbridge P, Liang C, Davis RL, Vandebona H, Sue CM. Woodbridge P, et al. Among authors: davis rl. Intern Med J. 2013 Feb;43(2):150-6. doi: 10.1111/j.1445-5994.2012.02847.x. Intern Med J. 2013. PMID: 22647225

4

Fibroblast growth factor 21 is a sensitive biomarker of mitochondrial disease.

Davis RL, Liang C, Edema-Hildebrand F, Riley C, Needham M, Sue CM. Davis RL, et al. Neurology. 2013 Nov 19;81(21):1819-26. doi: 10.1212/01.wnl.0000436068.43384.ef. Epub 2013 Oct 18. Neurology. 2013. PMID: 24142477

5

Systematic review of cardiac electrical disease in Kearns-Sayre syndrome and mitochondrial cytopathy.

Kabunga P, Lau AK, Phan K, Puranik R, Liang C, Davis RL, Sue CM, Sy RW. Kabunga P, et al. Among authors: davis rl. Int J Cardiol. 2015 Feb 15;181:303-10. doi: 10.1016/j.ijcard.2014.12.038. Epub 2014 Dec 13. Int J Cardiol. 2015. PMID: 25540845 Review.

6

A novel OPA1 mutation causing variable age of onset autosomal dominant optic atrophy plus in an Australian family.

Ahmad KE, Davis RL, Sue CM. Ahmad KE, et al. Among authors: davis rl. J Neurol. 2015 Oct;262(10):2323-8. doi: 10.1007/s00415-015-7849-6. Epub 2015 Jul 21. J Neurol. 2015. PMID: 26194196

7

Loss of ATP13A2 impairs glycolytic function in Kufor-Rakeb syndrome patient-derived cell models.

Park JS, Koentjoro B, Davis RL, Sue CM. Park JS, et al. Among authors: davis rl. Parkinsonism Relat Disord. 2016 Jun;27:67-73. doi: 10.1016/j.parkreldis.2016.03.018. Epub 2016 Mar 22. Parkinsonism Relat Disord. 2016. PMID: 27039055

8

A comparison of current serum biomarkers as diagnostic indicators of mitochondrial diseases.

Davis RL, Liang C, Sue CM. Davis RL, et al. Neurology. 2016 May 24;86(21):2010-5. doi: 10.1212/WNL.0000000000002705. Epub 2016 Apr 27. Neurology. 2016. PMID: 27164684 Free PMC article.

9

Mitochondrial diseases.

Davis RL, Liang C, Sue CM. Davis RL, et al. Handb Clin Neurol. 2018;147:125-141. doi: 10.1016/B978-0-444-63233-3.00010-5. Handb Clin Neurol. 2018. PMID: 29325608 Review.

10

Mitochondrial Dysfunction in Parkinson's Disease: New Mechanistic Insights and Therapeutic Perspectives.

Park JS, Davis RL, Sue CM. Park JS, et al. Among authors: davis rl. Curr Neurol Neurosci Rep. 2018 Apr 3;18(5):21. doi: 10.1007/s11910-018-0829-3. Curr Neurol Neurosci Rep. 2018. PMID: 29616350 Free PMC article. Review.

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