Hudson G - Search Results

1

The A467T and W748S POLG substitutions are a rare cause of adult-onset ataxia in Europe.

Craig K, Ferrari G, Tiangyou W, Hudson G, Gellera C, Zeviani M, Chinnery PF. Craig K, et al. Among authors: hudson g. Brain. 2007 Apr;130(Pt 4):E69; author reply E70. doi: 10.1093/brain/awm009. Brain. 2007. PMID: 17438011 No abstract available.

2

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: hudson g. Brain. 2006 Jul;129(Pt 7):1674-84. doi: 10.1093/brain/awl088. Epub 2006 Apr 18. Brain. 2006. PMID: 16621917

3

POLG1 in idiopathic Parkinson disease.

Tiangyou W, Hudson G, Ghezzi D, Ferrari G, Zeviani M, Burn DJ, Chinnery PF. Tiangyou W, et al. Among authors: hudson g. Neurology. 2006 Nov 14;67(9):1698-700. doi: 10.1212/01.wnl.0000238963.07425.d5. Epub 2006 Aug 30. Neurology. 2006. PMID: 16943369

4

Mitochondrial DNA polymerase-gamma and human disease.

Hudson G, Chinnery PF. Hudson G, et al. Hum Mol Genet. 2006 Oct 15;15 Spec No 2:R244-52. doi: 10.1093/hmg/ddl233. Hum Mol Genet. 2006. PMID: 16987890 Review.

5

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

6

No association between common POLG1 variants and sporadic idiopathic Parkinson's disease.

Hudson G, Tiangyou W, Stutt A, Eccles M, Robinson L, Burn DJ, Chinnery PF. Hudson G, et al. Mov Disord. 2009 May 15;24(7):1092-4. doi: 10.1002/mds.22310. Mov Disord. 2009. PMID: 19243043 No abstract available.

7

Does mitochondrial DNA predispose to neuromyelitis optica (Devic's disease)?

Hudson G, Mowbray C, Elson JL, Jacob A, Boggild M, Torroni A, Chinnery PF. Hudson G, et al. Brain. 2008 Apr;131(Pt 4):e93. doi: 10.1093/brain/awm224. Epub 2007 Oct 29. Brain. 2008. PMID: 17967805 Review. No abstract available.

8

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. Brain. 2008 Feb;131(Pt 2):329-37. doi: 10.1093/brain/awm272. Epub 2007 Dec 7. Brain. 2008. PMID: 18065439

9

Late-onset ptosis and myopathy in a patient with a heterozygous insertion in POLG2.

Walter MC, Czermin B, Muller-Ziermann S, Bulst S, Stewart JD, Hudson G, Schneiderat P, Abicht A, Holinski-Feder E, Lochmüller H, Chinnery PF, Klopstock T, Horvath R. Walter MC, et al. Among authors: hudson g. J Neurol. 2010 Sep;257(9):1517-23. doi: 10.1007/s00415-010-5565-9. Epub 2010 Apr 20. J Neurol. 2010. PMID: 20405137

10

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. 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.

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