Chinnery PF - Search Results

1

Chronic pain is common in mitochondrial disease.

van den Ameele J, Fuge J, Pitceathly RDS, Berry S, McIntyre Z, Hanna MG, Lee M, Chinnery PF. van den Ameele J, et al. Among authors: chinnery pf. Neuromuscul Disord. 2020 May;30(5):413-419. doi: 10.1016/j.nmd.2020.02.017. Epub 2020 Feb 29. Neuromuscul Disord. 2020. PMID: 32334903 Free PMC article.

2

Diagnostic utility of metabolic exercise testing in a patient with cardiovascular disease.

Elliott PM, Hanna MG, Ward SA, Chinnery PF, Turnbull DM, Wood NW, McKenna WJ. Elliott PM, et al. Among authors: chinnery pf. Heart. 1999 Apr;81(4):441-3. doi: 10.1136/hrt.81.4.441. Heart. 1999. PMID: 10092577 Free PMC article.

3

An mtDNA mutation in the initiation codon of the cytochrome C oxidase subunit II gene results in lower levels of the protein and a mitochondrial encephalomyopathy.

Clark KM, Taylor RW, Johnson MA, Chinnery PF, Chrzanowska-Lightowlers ZM, Andrews RM, Nelson IP, Wood NW, Lamont PJ, Hanna MG, Lightowlers RN, Turnbull DM. Clark KM, et al. Among authors: chinnery pf. Am J Hum Genet. 1999 May;64(5):1330-9. doi: 10.1086/302361. Am J Hum Genet. 1999. PMID: 10205264 Free PMC article.

4

Neuropathological and histochemical changes in a multiple mitochondrial DNA deletion disorder.

Cottrell DA, Ince PG, Blakely EL, Johnson MA, Chinnery PF, Hanna M, Turnbull DM. Cottrell DA, et al. Among authors: chinnery pf. J Neuropathol Exp Neurol. 2000 Jul;59(7):621-7. doi: 10.1093/jnen/59.7.621. J Neuropathol Exp Neurol. 2000. PMID: 10901234

5

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

6

116th ENMC international workshop: the treatment of mitochondrial disorders, 14th-16th March 2003, Naarden, The Netherlands.

Chinnery PF, Bindoff LA; Europen neuromuscular center. Chinnery PF, et al. Neuromuscul Disord. 2003 Nov;13(9):757-64. doi: 10.1016/s0960-8966(03)00097-x. Neuromuscul Disord. 2003. PMID: 14561500 Review. No abstract available.

7

Cytochrome c oxidase deficient muscle fibres: substantial variation in their proportions within skeletal muscles from patients with mitochondrial myopathy.

Barron MJ, Chinnery PF, Howel D, Blakely EL, Schaefer AM, Taylor RW, Turnbull DM. Barron MJ, et al. Among authors: chinnery pf. Neuromuscul Disord. 2005 Nov;15(11):768-74. doi: 10.1016/j.nmd.2005.06.018. Epub 2005 Sep 28. Neuromuscul Disord. 2005. PMID: 16198107

8

Phenotypic spectrum associated with mutations of the mitochondrial polymerase gamma gene.

Horvath R, Hudson G, Ferrari G, Fütterer N, Ahola S, Lamantea E, Prokisch H, Lochmüller H, McFarland R, Ramesh V, Klopstock T, Freisinger P, Salvi F, Mayr JA, Santer R, Tesarova M, Zeman J, Udd B, Taylor RW, Turnbull D, Hanna M, Fialho D, Suomalainen A, Zeviani M, Chinnery PF. Horvath R, et al. Among authors: chinnery pf. Brain. 2006 Jul;129(Pt 7):1674-84. doi: 10.1093/brain/awl088. Epub 2006 Apr 18. Brain. 2006. PMID: 16621917

9

POLG1, C10ORF2, and ANT1 mutations are uncommon in sporadic progressive external ophthalmoplegia with multiple mitochondrial DNA deletions.

Hudson G, Deschauer M, Taylor RW, Hanna MG, Fialho D, Schaefer AM, He LP, Blakely E, Turnbull DM, Chinnery PF. Hudson G, et al. Among authors: chinnery pf. Neurology. 2006 May 9;66(9):1439-41. doi: 10.1212/01.wnl.0000210486.32196.24. Neurology. 2006. PMID: 16682683

10

Prevalence of mitochondrial DNA disease in adults.

Schaefer AM, McFarland R, Blakely EL, He L, Whittaker RG, Taylor RW, Chinnery PF, Turnbull DM. Schaefer AM, et al. Among authors: chinnery pf. Ann Neurol. 2008 Jan;63(1):35-9. doi: 10.1002/ana.21217. Ann Neurol. 2008. PMID: 17886296

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