Chinnery PF - Search Results

1

Exome sequencing in dementia with Lewy bodies.

Keogh MJ, Kurzawa-Akanbi M, Griffin H, Douroudis K, Ayers KL, Hussein RI, Hudson G, Pyle A, Cordell HJ, Attems J, McKeith IG, O'Brien JT, Burn DJ, Morris CM, Thomas AJ, Chinnery PF. Keogh MJ, et al. Among authors: chinnery pf. Transl Psychiatry. 2016 Feb 2;6(2):e728. doi: 10.1038/tp.2015.220. Transl Psychiatry. 2016. PMID: 26836416 Free PMC article.

2

Management of parkinsonism and psychotic depression in a case of acute intermittent porphyria.

Chinnery PF, Cartlidge NE, Burn DJ, Cleland PG, McKeith I. Chinnery PF, et al. J Neurol Neurosurg Psychiatry. 1997 May;62(5):542. doi: 10.1136/jnnp.62.5.542. J Neurol Neurosurg Psychiatry. 1997. PMID: 9153622 Free PMC article. No abstract available.

3

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

4

Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease.

Curtis AR, Fey C, Morris CM, Bindoff LA, Ince PG, Chinnery PF, Coulthard A, Jackson MJ, Jackson AP, McHale DP, Hay D, Barker WA, Markham AF, Bates D, Curtis A, Burn J. Curtis AR, et al. Among authors: chinnery pf. Nat Genet. 2001 Aug;28(4):350-4. doi: 10.1038/ng571. Nat Genet. 2001. PMID: 11438811

5

Late-onset axial jerky dystonia due to the DYT1 deletion.

Chinnery PF, Reading PJ, McCarthy EL, Curtis A, Burn DJ. Chinnery PF, et al. Mov Disord. 2002 Jan;17(1):196-8. doi: 10.1002/mds.10021. Mov Disord. 2002. PMID: 11835464

6

No evidence of an association between the T16189C mtDNA variant and late onset dementia.

Gibson AM, Edwardson JA, Turnbull DM, McKeith IG, Morris CM, Chinnery PF. Gibson AM, et al. Among authors: chinnery pf. J Med Genet. 2004 Jan;41(1):e7. doi: 10.1136/jmg.2003.010983. J Med Genet. 2004. PMID: 14729847 Free PMC article. No abstract available.

7

Sensory ataxic neuropathy due to a novel C10Orf2 mutation with probable germline mosaicism.

Hudson G, Deschauer M, Busse K, Zierz S, Chinnery PF. Hudson G, et al. Among authors: chinnery pf. Neurology. 2005 Jan 25;64(2):371-3. doi: 10.1212/01.WNL.0000149767.51152.83. Neurology. 2005. PMID: 15668446

8

Mitochondrial DNA haplogroup cluster UKJT reduces the risk of PD.

Pyle A, Foltynie T, Tiangyou W, Lambert C, Keers SM, Allcock LM, Davison J, Lewis SJ, Perry RH, Barker R, Burn DJ, Chinnery PF. Pyle A, et al. Among authors: chinnery pf. Ann Neurol. 2005 Apr;57(4):564-7. doi: 10.1002/ana.20417. Ann Neurol. 2005. PMID: 15786469

9

Mitochondrial DNA and survival after sepsis: a prospective study.

Baudouin SV, Saunders D, Tiangyou W, Elson JL, Poynter J, Pyle A, Keers S, Turnbull DM, Howell N, Chinnery PF. Baudouin SV, et al. Among authors: chinnery pf. Lancet. 2005 Dec 17;366(9503):2118-21. doi: 10.1016/S0140-6736(05)67890-7. Lancet. 2005. PMID: 16360789

10

Allelic variation of a functional polymorphism in the serotonin transporter gene and depression in Parkinson's disease.

Burn DJ, Tiangyou W, Allcock LM, Davison J, Chinnery PF. Burn DJ, et al. Among authors: chinnery pf. Parkinsonism Relat Disord. 2006 Apr;12(3):139-41. doi: 10.1016/j.parkreldis.2005.11.005. Epub 2006 Feb 3. Parkinsonism Relat Disord. 2006. PMID: 16459126

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