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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: curtis ar, curtis 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: curtis ar, curtis 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
MLH1 Differential allelic expression in mutation carriers and controls.
Santibanez Koref M, Wilson V, Cartwright N, Cunnington MS, Mathers JC, Bishop DT, Curtis A, Dunlop MG, Burn J. Santibanez Koref M, et al. Among authors: curtis a. Ann Hum Genet. 2010 Nov;74(6):479-88. doi: 10.1111/j.1469-1809.2010.00603.x. Epub 2010 Sep 23. Ann Hum Genet. 2010. PMID: 20860725
Natural sampling and aliasing of marine geochemical signals.
Curtis A, Bloem H, Wood R, Bowyer F, Shields GA, Zhou Y, Yilales M, Tetzlaff D. Curtis A, et al. Sci Rep. 2025 Jan 4;15(1):760. doi: 10.1038/s41598-024-84871-6. Sci Rep. 2025. PMID: 39755753 Free PMC article.
1,795 results