Chinnery PF - Search Results

1

Minimum prevalence of spinocerebellar ataxia 17 in the north east of England.

Craig K, Keers SM, Walls TJ, Curtis A, Chinnery PF. Craig K, et al. Among authors: chinnery pf. J Neurol Sci. 2005 Dec 15;239(1):105-9. doi: 10.1016/j.jns.2005.08.009. Epub 2005 Oct 11. J Neurol Sci. 2005. PMID: 16223509

2

Recurrent strokes in a 34-year-old man.

Chinnery PF, Turnbull DM, Walls TJ, Reading PJ. Chinnery PF, et al. Lancet. 1997 Aug 23;350(9077):560. doi: 10.1016/s0140-6736(97)05005-8. Lancet. 1997. PMID: 9284779 No abstract available.

3

A novel autosomal dominant distal myopathy with early respiratory failure: clinico-pathologic characteristics and exclusion of linkage to candidate genetic loci.

Chinnery PF, Johnson MA, Walls TJ, Gibson GJ, Fawcett PR, Jamieson S, Fulthorpe JJ, Cullen M, Hudgson P, Bushby KM. Chinnery PF, et al. Ann Neurol. 2001 Apr;49(4):443-52. Ann Neurol. 2001. PMID: 11310621

4

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

5

Spinocerebellar ataxia and the A3243G and A8344G mtDNA mutations.

Chinnery PF, Brown DT, Archibald K, Curtis A, Turnbull DM. Chinnery PF, et al. J Med Genet. 2002 May;39(5):E22. doi: 10.1136/jmg.39.5.e22. J Med Genet. 2002. PMID: 12011163 Free PMC article. No abstract available.

6

Normokalemic periodic paralysis revisited: does it exist?

Chinnery PF, Walls TJ, Hanna MG, Bates D, Fawcett PR. Chinnery PF, et al. Ann Neurol. 2002 Aug;52(2):251-2. doi: 10.1002/ana.10257. Ann Neurol. 2002. PMID: 12210802

7

The epidemiology of Leber hereditary optic neuropathy in the North East of England.

Yu-Wai-Man P, Griffiths PG, Brown DT, Howell N, Turnbull DM, Chinnery PF. Yu-Wai-Man P, et al. Among authors: chinnery pf. Am J Hum Genet. 2003 Feb;72(2):333-9. doi: 10.1086/346066. Epub 2002 Jan 7. Am J Hum Genet. 2003. PMID: 12518276 Free PMC article.

8

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.

9

Clinical progression of mitochondrial myopathy is associated with the random accumulation of cytochrome c oxidase negative skeletal muscle fibres.

Chinnery PF, Howel D, Turnbull DM, Johnson MA. Chinnery PF, et al. J Neurol Sci. 2003 Jul 15;211(1-2):63-6. doi: 10.1016/s0022-510x(03)00039-x. J Neurol Sci. 2003. PMID: 12767499

10

The role of apolipoprotein E gene polymorphisms in primary open-angle glaucoma.

Ressiniotis T, Griffiths PG, Birch M, Keers S, Chinnery PF. Ressiniotis T, et al. Among authors: chinnery pf. Arch Ophthalmol. 2004 Feb;122(2):258-61. doi: 10.1001/archopht.122.2.258. Arch Ophthalmol. 2004. PMID: 14769603

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