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The spectrum of hearing loss due to mitochondrial DNA defects.
Chinnery PF, Elliott C, Green GR, Rees A, Coulthard A, Turnbull DM, Griffiths TD. Chinnery PF, et al. Among authors: coulthard a. Brain. 2000 Jan;123 ( Pt 1):82-92. doi: 10.1093/brain/123.1.82. Brain. 2000. PMID: 10611123
Neuroferritinopathy: a new inborn error of iron metabolism.
Keogh MJ, Jonas P, Coulthard A, Chinnery PF, Burn J. Keogh MJ, et al. Among authors: coulthard a. 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.
Neuroferritinopathy in a French family with late onset dominant dystonia.
Chinnery PF, Curtis AR, Fey C, Coulthard A, Crompton D, Curtis A, Lombés A, Burn J. Chinnery PF, et al. Among authors: coulthard a. J Med Genet. 2003 May;40(5):e69. doi: 10.1136/jmg.40.5.e69. J Med Genet. 2003. PMID: 12746423 Free PMC article. No abstract available.
Neuroferritinopathy: a window on the role of iron in neurodegeneration.
Crompton DE, Chinnery PF, Fey C, Curtis AR, Morris CM, Kierstan J, Burt A, Young F, Coulthard A, Curtis A, Ince PG, Bates D, Jackson MJ, Burn J. Crompton DE, et al. Among authors: coulthard a. Blood Cells Mol Dis. 2002 Nov-Dec;29(3):522-31. doi: 10.1006/bcmd.2002.0589. Blood Cells Mol Dis. 2002. PMID: 12547246
Familial cavernous angiomas masquerading as multiple sclerosis.
Dougan CF, Coulthard A, Cartlidge NE, Burn DJ. Dougan CF, et al. Among authors: coulthard a. Postgrad Med J. 1998 Aug;74(874):489-91. doi: 10.1136/pgmj.74.874.489. Postgrad Med J. 1998. PMID: 9926126 Free PMC article.
189 results