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Page 1
COX10 mutations resulting in complex multisystem mitochondrial disease that remains stable into adulthood.
Pitceathly RD, Taanman JW, Rahman S, Meunier B, Sadowski M, Cirak S, Hargreaves I, Land JM, Nanji T, Polke JM, Woodward CE, Sweeney MG, Solanki S, Foley AR, Hurles ME, Stalker J, Blake J, Holton JL, Phadke R, Muntoni F, Reilly MM, Hanna MG; UK10K Consortium. Pitceathly RD, et al. Among authors: reilly mm. JAMA Neurol. 2013 Dec;70(12):1556-61. doi: 10.1001/jamaneurol.2013.3242. JAMA Neurol. 2013. PMID: 24100867
Genetic neuromuscular disease.
Reilly MM, Hanna MG. Reilly MM, et al. J Neurol Neurosurg Psychiatry. 2002 Dec;73 Suppl 2(Suppl 2):II12-21. doi: 10.1136/jnnp.73.suppl_2.ii12. J Neurol Neurosurg Psychiatry. 2002. PMID: 12536154 Free PMC article. Review. No abstract available.
Hereditary sensory neuropathies.
Houlden H, Blake J, Reilly MM. Houlden H, et al. Among authors: reilly mm. Curr Opin Neurol. 2004 Oct;17(5):569-77. doi: 10.1097/00019052-200410000-00007. Curr Opin Neurol. 2004. PMID: 15367861 Review.
Copper deficiency as a treatable cause of poor balance.
Khaleeli Z, Healy DG, Briddon A, Lunn MP, Reilly MM, Land J, Giovannoni G. Khaleeli Z, et al. Among authors: reilly mm. BMJ. 2010 Apr 12;340:c508. doi: 10.1136/bmj.c508. BMJ. 2010. PMID: 20385722 No abstract available.
[Copper deficiency as a treatable cause of poor balance].
Khaleeli Z, Healy DG, Briddon A, Lunn MP, Reilly MM, Land J, Giovannoni G. Khaleeli Z, et al. Among authors: reilly mm. Praxis (Bern 1994). 2010 Sep 22;99(19):1153-6. doi: 10.1024/1661-8157/a000258. Praxis (Bern 1994). 2010. PMID: 20859879 German. No abstract available.
419 results