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Mitochondrial DNA mutations in neurodegeneration.
Keogh MJ, Chinnery PF. Keogh MJ, et al. Biochim Biophys Acta. 2015 Nov;1847(11):1401-11. doi: 10.1016/j.bbabio.2015.05.015. Epub 2015 May 23. Biochim Biophys Acta. 2015. PMID: 26014345 Free article. Review.
Neuroferritinopathy: a new inborn error of iron metabolism.
Keogh MJ, Jonas P, Coulthard A, Chinnery PF, Burn J. Keogh MJ, et al. Neurogenetics. 2012 Feb;13(1):93-6. doi: 10.1007/s10048-011-0310-9. Epub 2012 Jan 26. Neurogenetics. 2012. PMID: 22278127 Free PMC article.
Early neuropsychiatry features in neuroferritinopathy.
Keogh MJ, Singh B, Chinnery PF. Keogh MJ, et al. Mov Disord. 2013 Aug;28(9):1310-3. doi: 10.1002/mds.25371. Epub 2013 Feb 23. Mov Disord. 2013. PMID: 23436236 No abstract available.
How to spot mitochondrial disease in adults.
Keogh MJ, Chinnery PF. Keogh MJ, et al. Clin Med (Lond). 2013 Feb;13(1):87-92. doi: 10.7861/clinmedicine.13-1-87. Clin Med (Lond). 2013. PMID: 23472503 Free PMC article. Review. No abstract available.
Exome sequencing: how to understand it.
Keogh MJ, Daud D, Chinnery PF. Keogh MJ, et al. Pract Neurol. 2013 Dec;13(6):399-407. doi: 10.1136/practneurol-2012-000498. Epub 2013 Jun 1. Pract Neurol. 2013. PMID: 23727621 Review. No abstract available.
69 results