Simon DK - Search Results

1

Mitochondrial DNA mutations in complex I and tRNA genes in Parkinson's disease.

Simon DK, Mayeux R, Marder K, Kowall NW, Beal MF, Johns DR. Simon DK, et al. Neurology. 2000 Feb 8;54(3):703-9. doi: 10.1212/wnl.54.3.703. Neurology. 2000. PMID: 10680807

2

Mitochondrial disorders: clinical and genetic features.

Simon DK, Johns DR. Simon DK, et al. Annu Rev Med. 1999;50:111-27. doi: 10.1146/annurev.med.50.1.111. Annu Rev Med. 1999. PMID: 10073267 Review.

3

Familial multisystem degeneration with parkinsonism associated with the 11778 mitochondrial DNA mutation.

Simon DK, Pulst SM, Sutton JP, Browne SE, Beal MF, Johns DR. Simon DK, et al. Neurology. 1999 Nov 10;53(8):1787-93. doi: 10.1212/wnl.53.8.1787. Neurology. 1999. PMID: 10563629

4

Low mutational burden of individual acquired mitochondrial DNA mutations in brain.

Simon DK, Lin MT, Ahn CH, Liu GJ, Gibson GE, Beal MF, Johns DR. Simon DK, et al. Genomics. 2001 Apr 1;73(1):113-6. doi: 10.1006/geno.2001.6515. Genomics. 2001. PMID: 11352572

5

Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.

Pankratz N, Beecham GW, DeStefano AL, Dawson TM, Doheny KF, Factor SA, Hamza TH, Hung AY, Hyman BT, Ivinson AJ, Krainc D, Latourelle JC, Clark LN, Marder K, Martin ER, Mayeux R, Ross OA, Scherzer CR, Simon DK, Tanner C, Vance JM, Wszolek ZK, Zabetian CP, Myers RH, Payami H, Scott WK, Foroud T; PD GWAS Consortium. Pankratz N, et al. Among authors: simon dk. Ann Neurol. 2012 Mar;71(3):370-84. doi: 10.1002/ana.22687. Ann Neurol. 2012. PMID: 22451204 Free PMC article.

6

Mitochondrial DNA haplogroups and mutations in children with acquired central demyelination.

Venkateswaran S, Zheng K, Sacchetti M, Gagne D, Arnold DL, Sadovnick AD, Scherer SW, Banwell B, Bar-Or A, Simon DK; Canadian Pediatric Demyelinating Disease Network. Venkateswaran S, et al. Among authors: simon dk. Neurology. 2011 Mar 1;76(9):774-80. doi: 10.1212/WNL.0b013e31820ee1bb. Epub 2011 Feb 2. Neurology. 2011. PMID: 21288980 Free PMC article.

7

A frameshift mitochondrial complex I gene mutation in a patient with dystonia and cataracts: is the mutation pathogenic?

Simon DK, Tarnopolsky MA, Greenamyre JT, Johns DR. Simon DK, et al. J Med Genet. 2001 Jan;38(1):58-61. doi: 10.1136/jmg.38.1.58. J Med Genet. 2001. PMID: 11332403 Free PMC article. No abstract available.

8

Novel SCO2 mutation (G1521A) presenting as a spinal muscular atrophy type I phenotype.

Tarnopolsky MA, Bourgeois JM, Fu MH, Kataeva G, Shah J, Simon DK, Mahoney D, Johns D, MacKay N, Robinson BH. Tarnopolsky MA, et al. Among authors: simon dk. Am J Med Genet A. 2004 Mar 15;125A(3):310-4. doi: 10.1002/ajmg.a.20466. Am J Med Genet A. 2004. PMID: 14994243

9

Non-invasive brain stimulation for Parkinson's disease: a systematic review and meta-analysis of the literature.

Fregni F, Simon DK, Wu A, Pascual-Leone A. Fregni F, et al. Among authors: simon dk. J Neurol Neurosurg Psychiatry. 2005 Dec;76(12):1614-23. doi: 10.1136/jnnp.2005.069849. J Neurol Neurosurg Psychiatry. 2005. PMID: 16291882 Free PMC article. Review.

10

Novel THAP1 sequence variants in primary dystonia.

Xiao J, Zhao Y, Bastian RW, Perlmutter JS, Racette BA, Tabbal SD, Karimi M, Paniello RC, Wszolek ZK, Uitti RJ, Van Gerpen JA, Simon DK, Tarsy D, Hedera P, Truong DD, Frei KP, Dev Batish S, Blitzer A, Pfeiffer RF, Gong S, LeDoux MS. Xiao J, et al. Among authors: simon dk. Neurology. 2010 Jan 19;74(3):229-38. doi: 10.1212/WNL.0b013e3181ca00ca. Neurology. 2010. PMID: 20083799 Free PMC article.

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