Chinnery PF - Search Results

1

SCP2 mutations and neurodegeneration with brain iron accumulation.

Horvath R, Lewis-Smith D, Douroudis K, Duff J, Keogh M, Pyle A, Fletcher N, Chinnery PF. Horvath R, et al. Among authors: chinnery pf. Neurology. 2015 Nov 24;85(21):1909-11. doi: 10.1212/WNL.0000000000002157. Epub 2015 Oct 23. Neurology. 2015. PMID: 26497993 Free PMC article. No abstract available.

2

A novel mitochondrial tRNA isoleucine gene mutation causing chronic progressive external ophthalmoplegia.

Chinnery PF, Johnson MA, Taylor RW, Durward WF, Turnbull DM. Chinnery PF, et al. Neurology. 1997 Oct;49(4):1166-8. doi: 10.1212/wnl.49.4.1166. Neurology. 1997. PMID: 9339712

3

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

4

Mitochondrial DNA haplogroups and susceptibility to AD and dementia with Lewy bodies.

Chinnery PF, Taylor GA, Howell N, Andrews RM, Morris CM, Taylor RW, McKeith IG, Perry RH, Edwardson JA, Turnbull DM. Chinnery PF, et al. Neurology. 2000 Jul 25;55(2):302-4. doi: 10.1212/wnl.55.2.302. Neurology. 2000. PMID: 10908912

5

The epidemiology of pathogenic mitochondrial DNA mutations.

Chinnery PF, Johnson MA, Wardell TM, Singh-Kler R, Hayes C, Brown DT, Taylor RW, Bindoff LA, Turnbull DM. Chinnery PF, et al. Ann Neurol. 2000 Aug;48(2):188-93. Ann Neurol. 2000. PMID: 10939569

6

The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy.

Chinnery PF, Brown DT, Andrews RM, Singh-Kler R, Riordan-Eva P, Lindley J, Applegarth DA, Turnbull DM, Howell N. Chinnery PF, et al. Brain. 2001 Jan;124(Pt 1):209-18. doi: 10.1093/brain/124.1.209. Brain. 2001. PMID: 11133798

7

No correlation between muscle A3243G mutation load and mitochondrial function in vivo.

Chinnery PF, Taylor DJ, Manners D, Styles P, Lodi R. Chinnery PF, et al. Neurology. 2001 Apr 24;56(8):1101-4. doi: 10.1212/wnl.56.8.1101. Neurology. 2001. PMID: 11320187

8

NDUFA-1 is not a nuclear modifier gene in Leber hereditary optic neuropathy.

Yu-Wai-Man P, Brown DT, Wehnert MS, Zeviani M, Carrara F, Turnbull DM, Chinnery PF. Yu-Wai-Man P, et al. Among authors: chinnery pf. Neurology. 2002 Jun 25;58(12):1861-2. doi: 10.1212/wnl.58.12.1861. Neurology. 2002. PMID: 12084895 No abstract available.

9

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

10

Limbic encephalitis: Not a picture to forget.

Chinnery PF, Cottrell DA, Birchall D, Griffiths TD. Chinnery PF, et al. Neurology. 2004 Mar 23;62(6):1019. doi: 10.1212/01.wnl.0000101678.44738.4b. Neurology. 2004. PMID: 15037718 No abstract available.

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