Griffiths PG - Search Results

1

Apolipoprotein E promoter polymorphisms do not have a major influence on the risk of developing primary open angle glaucoma.

Ressiniotis T, Griffiths PG, Birch M, Keers SM, Chinnery PF. Ressiniotis T, et al. Among authors: griffiths pg. Mol Vis. 2004 Oct 28;10:805-7. Mol Vis. 2004. PMID: 15525904 Free article.

2

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: griffiths pg. Arch Ophthalmol. 2004 Feb;122(2):258-61. doi: 10.1001/archopht.122.2.258. Arch Ophthalmol. 2004. PMID: 14769603

3

A polymorphism at codon 31 of gene p21 is not associated with primary open angle glaucoma in Caucasians.

Ressiniotis T, Griffiths PG, Keers SM, Chinnery PF, Birch M. Ressiniotis T, et al. Among authors: griffiths pg. BMC Ophthalmol. 2005 Apr 4;5:5. doi: 10.1186/1471-2415-5-5. BMC Ophthalmol. 2005. PMID: 15807891 Free PMC article.

4

Identification of an X-chromosomal locus and haplotype modulating the phenotype of a mitochondrial DNA disorder.

Hudson G, Keers S, Yu-Wai-Man P, Griffiths P, Huoponen K, Savontaus ML, Nikoskelainen E, Zeviani M, Carrara F, Horvath R, Karcagi V, Spruijt L, de Coo IF, Smeets HJ, Chinnery PF. Hudson G, et al. Am J Hum Genet. 2005 Dec;77(6):1086-91. doi: 10.1086/498176. Epub 2005 Oct 11. Am J Hum Genet. 2005. PMID: 16380918 Free PMC article.

5

Investigation of auditory dysfunction in Leber hereditary optic neuropathy.

Yu-Wai-Man P, Elliott C, Griffiths PG, Johnson IJ, Chinnery PF. Yu-Wai-Man P, et al. Among authors: griffiths pg. Acta Ophthalmol. 2008 Sep;86(6):630-3. doi: 10.1111/j.1600-0420.2007.01078.x. Acta Ophthalmol. 2008. PMID: 18070226 Free article.

6

Variation in MAPT is not a contributing factor to the incomplete penetrance in LHON.

Hudson G, Yu-Wai-Man P, Griffiths PG, Horvath R, Carelli V, Zeviani M, Chinnery PF. Hudson G, et al. Among authors: griffiths pg. Mitochondrion. 2011 Jul;11(4):620-2. doi: 10.1016/j.mito.2011.03.004. Epub 2011 Mar 21. Mitochondrion. 2011. PMID: 21397051 Free PMC article.

7

Raised intraocular pressure as a potential risk factor for visual loss in Leber Hereditary Optic Neuropathy.

Thouin A, Griffiths PG, Hudson G, Chinnery PF, Yu-Wai-Man P. Thouin A, et al. Among authors: griffiths pg. PLoS One. 2013 May 7;8(5):e63446. doi: 10.1371/journal.pone.0063446. Print 2013. PLoS One. 2013. PMID: 23667621 Free PMC article.

8

Mutation of the linker region of the polymerase gamma-1 (POLG1) gene associated with progressive external ophthalmoplegia and Parkinsonism.

Hudson G, Schaefer AM, Taylor RW, Tiangyou W, Gibson A, Venables G, Griffiths P, Burn DJ, Turnbull DM, Chinnery PF. Hudson G, et al. Arch Neurol. 2007 Apr;64(4):553-7. doi: 10.1001/archneur.64.4.553. Arch Neurol. 2007. PMID: 17420318

9

Short-term effects of focal argon laser treatment in diabetic maculopathy as demonstrated by optical coherence tomography.

Sandhu SS, Birch MK, Griffiths PG, Talks SJ. Sandhu SS, et al. Among authors: griffiths pg. Retina. 2007 Jan;27(1):13-20. doi: 10.1097/01.iae.0000256657.64240.a1. Retina. 2007. PMID: 17218910

10

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.

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