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Iron - Too Much of a Good Thing
Published online by Cambridge University Press: 02 December 2014
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- Copyright © The Canadian Journal of Neurological 2012
References
1Zecca, L, Youdim, MBH, Riederer, P, Connor, JR, Crichton, RR.Iron, brain ageing and neurodegenerative disorders. Nat Rev Neurosci. 2004; 5(11): 863–73.Google Scholar
2Hayflick, SJ, Westaway, SK, Levinson, B, et al.Genetic, clinical, and radiographic delineation of Hallervorden-Spatz syndrome. N Engl J Med. 2003; 348(1): 33–40.Google Scholar
3Schneider, SA, Hardy, J, Bhatia, KP.Syndromes of neurodegeneration with brain iron accumulation (NBIA): an update on clinical presentations, histological and genetic underpinnings, and treatment considerations. Mov Disord. 2012; 27(1): 42–53.Google Scholar
4Gregory, A, Hayflick, SJ.Genetics of neurodegeneration with brain iron accumulation. Curr Neurol Neurosci Rep. 2011; 11(3): 254–61.CrossRefGoogle ScholarPubMed
5Kruer, MC, Boddaert, N, Schneider, SA, et al.Neuroimaging features of neurodegeneration with brain iron accumulation. AJNR Am J Neuroradiol. 2011; Sep 15 as 10.3174/ajnr.A2677 [Epub ahead of print].Google Scholar
6Kurian, MA, McNeill, A, Lin, JP, Maher, ER.Childhood disorders of neurodegeneration with brain iron accumulation (NBIA). Dev Med Child Neurol. 2011; 53(5): 394–404.Google Scholar
7Birbes, H, Bawab, SE, Obeid, LM, Hannun, YA.Mitochondria and ceramide: intertwined roles in regulation of apoptosis. Advan Enzyme Regul. 2002; 42: 113–29.Google Scholar
8Bras, J, Singleton, A, Cookson, MR, Hardy, J.Emerging pathways in genetic Parkinson’s disease: potential role of ceramide metabolism in Lewy body disease. FEBS J. 2008; 275(23): 5767–73.Google Scholar
9Zhou, B, Westaway, SK, Levinson, B, Johnson, MA, Gitschier, J, Hayflick, SJ.A novel pantothenate kinase gene (PANK2) is defective in Hallervorden-Spatz syndrome. Nat Genet. 2001; 28(4): 345–9.Google Scholar
10Kim, J, Cho, JW, Shin, H, Yoon, J, Ki, CS, Cho, AR.A novel PANK2 gene mutation with sudden-onset dystonia like psychogenic movement. Can J Neurol Sci. 2012; 39(3):395–7.Google Scholar