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Page 1
Optic mitochondriopathies.
Chinnery PF, Griffiths PG. Chinnery PF, et al. Among authors: griffiths pg. Neurology. 2005 Mar 22;64(6):940-1. doi: 10.1212/01.WNL.0000157285.93611.B2. Neurology. 2005. PMID: 15781804 No abstract available.
Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance.
Hudson G, Amati-Bonneau P, Blakely EL, Stewart JD, He L, Schaefer AM, Griffiths PG, Ahlqvist K, Suomalainen A, Reynier P, McFarland R, Turnbull DM, Chinnery PF, Taylor RW. Hudson G, et al. Among authors: griffiths pg. Brain. 2008 Feb;131(Pt 2):329-37. doi: 10.1093/brain/awm272. Epub 2007 Dec 7. Brain. 2008. PMID: 18065439
The prevalence and natural history of dominant optic atrophy due to OPA1 mutations.
Yu-Wai-Man P, Griffiths PG, Burke A, Sellar PW, Clarke MP, Gnanaraj L, Ah-Kine D, Hudson G, Czermin B, Taylor RW, Horvath R, Chinnery PF. Yu-Wai-Man P, et al. Among authors: griffiths pg. Ophthalmology. 2010 Aug;117(8):1538-46, 1546.e1. doi: 10.1016/j.ophtha.2009.12.038. Epub 2010 Apr 24. Ophthalmology. 2010. PMID: 20417570 Free PMC article.
A randomized placebo-controlled trial of idebenone in Leber's hereditary optic neuropathy.
Klopstock T, Yu-Wai-Man P, Dimitriadis K, Rouleau J, Heck S, Bailie M, Atawan A, Chattopadhyay S, Schubert M, Garip A, Kernt M, Petraki D, Rummey C, Leinonen M, Metz G, Griffiths PG, Meier T, Chinnery PF. Klopstock T, et al. Among authors: griffiths pg. Brain. 2011 Sep;134(Pt 9):2677-86. doi: 10.1093/brain/awr170. Epub 2011 Jul 25. Brain. 2011. PMID: 21788663 Free PMC article. Clinical Trial.
Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background.
Hudson G, Carelli V, Spruijt L, Gerards M, Mowbray C, Achilli A, Pyle A, Elson J, Howell N, La Morgia C, Valentino ML, Huoponen K, Savontaus ML, Nikoskelainen E, Sadun AA, Salomao SR, Belfort R Jr, Griffiths P, Yu-Wai-Man P, de Coo RF, Horvath R, Zeviani M, Smeets HJ, Torroni A, Chinnery PF. Hudson G, et al. Am J Hum Genet. 2007 Aug;81(2):228-33. doi: 10.1086/519394. Epub 2007 Jun 4. Am J Hum Genet. 2007. PMID: 17668373 Free PMC article.
Leber hereditary optic neuropathy presenting in a 75-year-old man.
Yu-Wai-Man P, Bateman DE, Hudson G, Griffiths PG, Chinnery PF. Yu-Wai-Man P, et al. Among authors: griffiths pg. J Neuroophthalmol. 2008 Jun;28(2):155. doi: 10.1097/WNO.0b013e3181772db4. J Neuroophthalmol. 2008. PMID: 18562849 No abstract available.
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