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51 results
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A review of femoroacetabular impingement in athletes.
Keogh MJ, Batt ME. Keogh MJ, et al. Sports Med. 2008;38(10):863-78. doi: 10.2165/00007256-200838100-00005. Sports Med. 2008. PMID: 18803437 Review.
Reversible hypomagnesaemia-induced subacute cerebellar syndrome.
Sedehizadeh S, Keogh M, Wills AJ. Sedehizadeh S, et al. Biol Trace Elem Res. 2011 Aug;142(2):127-9. doi: 10.1007/s12011-010-8757-3. Epub 2010 Jul 7. Biol Trace Elem Res. 2011. PMID: 20607440
Specific interaction of hepatitis C virus glycoproteins with mannan binding lectin inhibits virus entry.
Brown KS, Keogh MJ, Owsianka AM, Adair R, Patel AH, Arnold JN, Ball JK, Sim RB, Tarr AW, Hickling TP. Brown KS, et al. Among authors: keogh mj. Protein Cell. 2010 Jul;1(7):664-74. doi: 10.1007/s13238-010-0088-9. Epub 2010 Jul 29. Protein Cell. 2010. PMID: 21203938 Free PMC article.
The use of aminopyridines in neurological disorders.
Sedehizadeh S, Keogh M, Maddison P. Sedehizadeh S, et al. Clin Neuropharmacol. 2012 Jul-Aug;35(4):191-200. doi: 10.1097/WNF.0b013e31825a68c5. Clin Neuropharmacol. 2012. PMID: 22805230 Review.
SCP2 mutations and neurodegeneration with brain iron accumulation.
Horvath R, Lewis-Smith D, Douroudis K, Duff J, Keogh M, Pyle A, Fletcher N, Chinnery PF. Horvath R, et al. Neurology. 2015 Nov 24;85(21):1909-11. doi: 10.1212/WNL.0000000000002157. Epub 2015 Oct 23. Neurology. 2015. PMID: 26497993 Free PMC article. No abstract available.
Treatment for Lambert-Eaton myasthenic syndrome.
Keogh M, Sedehizadeh S, Maddison P. Keogh M, et al. Cochrane Database Syst Rev. 2011 Feb 16;2011(2):CD003279. doi: 10.1002/14651858.CD003279.pub3. Cochrane Database Syst Rev. 2011. PMID: 21328260 Free PMC article. Review.
Next generation sequencing for neurological diseases: new hope or new hype?
Keogh MJ, Chinnery PF. Keogh MJ, et al. Clin Neurol Neurosurg. 2013 Jul;115(7):948-53. doi: 10.1016/j.clineuro.2012.09.030. Epub 2012 Nov 30. Clin Neurol Neurosurg. 2013. PMID: 23200550 Free PMC article. Review.
Neuroferritinopathy.
Keogh MJ, Morris CM, Chinnery PF. Keogh MJ, et al. Int Rev Neurobiol. 2013;110:91-123. doi: 10.1016/B978-0-12-410502-7.00006-5. Int Rev Neurobiol. 2013. PMID: 24209436 Review.
Hereditary mtDNA heteroplasmy: a baseline for aging?
Keogh M, Chinnery PF. Keogh M, et al. Cell Metab. 2013 Oct 1;18(4):463-4. doi: 10.1016/j.cmet.2013.09.015. Cell Metab. 2013. PMID: 24093673
High prevalence of focal and multi-focal somatic genetic variants in the human brain.
Keogh MJ, Wei W, Aryaman J, Walker L, van den Ameele J, Coxhead J, Wilson I, Bashton M, Beck J, West J, Chen R, Haudenschild C, Bartha G, Luo S, Morris CM, Jones NS, Attems J, Chinnery PF. Keogh MJ, et al. Nat Commun. 2018 Oct 15;9(1):4257. doi: 10.1038/s41467-018-06331-w. Nat Commun. 2018. PMID: 30323172 Free PMC article.
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