Chinnery PF - Search Results

1

Neuroferritinopathy: a new inborn error of iron metabolism.

Keogh MJ, Jonas P, Coulthard A, Chinnery PF, Burn J. Keogh MJ, et al. Among authors: chinnery pf. 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.

2

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. Brain. 2000 Jan;123 ( Pt 1):82-92. doi: 10.1093/brain/123.1.82. Brain. 2000. PMID: 10611123

3

Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease.

Curtis AR, Fey C, Morris CM, Bindoff LA, Ince PG, Chinnery PF, Coulthard A, Jackson MJ, Jackson AP, McHale DP, Hay D, Barker WA, Markham AF, Bates D, Curtis A, Burn J. Curtis AR, et al. Among authors: chinnery pf. Nat Genet. 2001 Aug;28(4):350-4. doi: 10.1038/ng571. Nat Genet. 2001. PMID: 11438811

4

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: chinnery pf. Blood Cells Mol Dis. 2002 Nov-Dec;29(3):522-31. doi: 10.1006/bcmd.2002.0589. Blood Cells Mol Dis. 2002. PMID: 12547246

5

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. 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.

6

Spectrum of movement disorders in neuroferritinopathy.

Crompton DE, Chinnery PF, Bates D, Walls TJ, Jackson MJ, Curtis AJ, Burn J. Crompton DE, et al. Among authors: chinnery pf. Mov Disord. 2005 Jan;20(1):95-9. doi: 10.1002/mds.20284. Mov Disord. 2005. PMID: 15390132

7

Neuroferritinopathy.

Burn J, Chinnery PF. Burn J, et al. Among authors: chinnery pf. Semin Pediatr Neurol. 2006 Sep;13(3):176-81. doi: 10.1016/j.spen.2006.08.006. Semin Pediatr Neurol. 2006. PMID: 17101456

8

Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutation.

Chinnery PF, Crompton DE, Birchall D, Jackson MJ, Coulthard A, Lombès A, Quinn N, Wills A, Fletcher N, Mottershead JP, Cooper P, Kellett M, Bates D, Burn J. Chinnery PF, et al. Brain. 2007 Jan;130(Pt 1):110-9. doi: 10.1093/brain/awl319. Epub 2006 Dec 2. Brain. 2007. PMID: 17142829

9

T2* and FSE MRI distinguishes four subtypes of neurodegeneration with brain iron accumulation.

McNeill A, Birchall D, Hayflick SJ, Gregory A, Schenk JF, Zimmerman EA, Shang H, Miyajima H, Chinnery PF. McNeill A, et al. Among authors: chinnery pf. Neurology. 2008 Apr 29;70(18):1614-9. doi: 10.1212/01.wnl.0000310985.40011.d6. Neurology. 2008. PMID: 18443312 Free PMC article.

10

Clinical features and natural history of neuroferritinopathy caused by the 458dupA FTL mutation.

Devos D, Tchofo PJ, Vuillaume I, Destée A, Batey S, Burn J, Chinnery PF. Devos D, et al. Among authors: chinnery pf. Brain. 2009 Jun;132(Pt 6):e109. doi: 10.1093/brain/awn274. Epub 2008 Oct 14. Brain. 2009. PMID: 18854324 Free PMC article. No abstract available.

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