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Items: 1 to 20 of 38

1.

Maternal inheritance and mitochondrial DNA variants in familial Parkinson's disease.

Simon DK, Pankratz N, Kissell DK, Pauciulo MW, Halter CA, Rudolph A, Pfeiffer RF, Nichols WC, Foroud T; Parkinson Study Group-PROGENI Investigators.

BMC Med Genet. 2010 Apr 1;11:53. doi: 10.1186/1471-2350-11-53.

2.

Incidence of acquired demyelination of the CNS in Canadian children.

Banwell B, Kennedy J, Sadovnick D, Arnold DL, Magalhaes S, Wambera K, Connolly MB, Yager J, Mah JK, Shah N, Sebire G, Meaney B, Dilenge ME, Lortie A, Whiting S, Doja A, Levin S, MacDonald EA, Meek D, Wood E, Lowry N, Buckley D, Yim C, Awuku M, Guimond C, Cooper P, Grand'Maison F, Baird JB, Bhan V, Bar-Or A.

Neurology. 2009 Jan 20;72(3):232-9. doi: 10.1212/01.wnl.0000339482.84392.bd.

PMID:
19153370
3.

Mitochondrial disease in autism spectrum disorder patients: a cohort analysis.

Weissman JR, Kelley RI, Bauman ML, Cohen BH, Murray KF, Mitchell RL, Kern RL, Natowicz MR.

PLoS One. 2008;3(11):e3815. doi: 10.1371/journal.pone.0003815. Epub 2008 Nov 26.

4.

Association of common mitochondrial DNA variants with multiple sclerosis and systemic lupus erythematosus.

Vyshkina T, Sylvester A, Sadiq S, Bonilla E, Canter JA, Perl A, Kalman B.

Clin Immunol. 2008 Oct;129(1):31-5. doi: 10.1016/j.clim.2008.07.011. Epub 2008 Aug 16.

5.

Mitochondrial complex I gene variant associated with early age at onset in spinocerebellar ataxia type 2.

Simon DK, Zheng K, Velázquez L, Santos N, Almaguer L, Figueroa KP, Pulst SM.

Arch Neurol. 2007 Jul;64(7):1042-4.

PMID:
17620498
6.

The involvement of mitochondria in the pathogenesis of multiple sclerosis.

Kalman B, Laitinen K, Komoly S.

J Neuroimmunol. 2007 Aug;188(1-2):1-12. Epub 2007 May 9. Review.

PMID:
17493689
7.

Consensus definitions proposed for pediatric multiple sclerosis and related disorders.

Krupp LB, Banwell B, Tenembaum S; International Pediatric MS Study Group.

Neurology. 2007 Apr 17;68(16 Suppl 2):S7-12. Review.

PMID:
17438241
8.

Mapping autism risk loci using genetic linkage and chromosomal rearrangements.

Autism Genome Project Consortium, Szatmari P, Paterson AD, Zwaigenbaum L, Roberts W, Brian J, Liu XQ, Vincent JB, Skaug JL, Thompson AP, Senman L, Feuk L, Qian C, Bryson SE, Jones MB, Marshall CR, Scherer SW, Vieland VJ, Bartlett C, Mangin LV, Goedken R, Segre A, Pericak-Vance MA, Cuccaro ML, Gilbert JR, Wright HH, Abramson RK, Betancur C, Bourgeron T, Gillberg C, Leboyer M, Buxbaum JD, Davis KL, Hollander E, Silverman JM, Hallmayer J, Lotspeich L, Sutcliffe JS, Haines JL, Folstein SE, Piven J, Wassink TH, Sheffield V, Geschwind DH, Bucan M, Brown WT, Cantor RM, Constantino JN, Gilliam TC, Herbert M, Lajonchere C, Ledbetter DH, Lese-Martin C, Miller J, Nelson S, Samango-Sprouse CA, Spence S, State M, Tanzi RE, Coon H, Dawson G, Devlin B, Estes A, Flodman P, Klei L, McMahon WM, Minshew N, Munson J, Korvatska E, Rodier PM, Schellenberg GD, Smith M, Spence MA, Stodgell C, Tepper PG, Wijsman EM, Yu CE, Rogé B, Mantoulan C, Wittemeyer K, Poustka A, Felder B, Klauck SM, Schuster C, Poustka F, Bölte S, Feineis-Matthews S, Herbrecht E, Schmötzer G, Tsiantis J, Papanikolaou K, Maestrini E, Bacchelli E, Blasi F, Carone S, Toma C, Van Engeland H, de Jonge M, Kemner C, Koop F, Langemeijer M, Hijmans C, Staal WG, Baird G, Bolton PF, Rutter ML, Weisblatt E, Green J, Aldred C, Wilkinson JA, Pickles A, Le Couteur A, Berney T, McConachie H, Bailey AJ, Francis K, Honeyman G, Hutchinson A, Parr JR, Wallace S, Monaco AP, Barnby G, Kobayashi K, Lamb JA, Sousa I, Sykes N, Cook EH, Guter SJ, Leventhal BL, Salt J, Lord C, Corsello C, Hus V, Weeks DE, Volkmar F, Tauber M, Fombonne E, Shih A, Meyer KJ.

Nat Genet. 2007 Mar;39(3):319-28. Epub 2007 Feb 18. Erratum in: Nat Genet. 2007 Oct;39(10):1285. Meyer, Kacie J [added]; Koop, Frederike [corrected to Koop, Frederieke]; Langemeijer, Marjolijn [corrected to Langemeijer, Marjolein]; Hijimans, Channa [corrected to Hijmans, Channa].

9.

mtDNA mutations and common neurodegenerative disorders.

Howell N, Elson JL, Chinnery PF, Turnbull DM.

Trends Genet. 2005 Nov;21(11):583-6. Epub 2005 Sep 8. Review.

PMID:
16154228
10.

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.

Ann Neurol. 2005 Apr;57(4):564-7.

PMID:
15786469
11.

Mitochondrial dysfunction in autism spectrum disorders: a population-based study.

Oliveira G, Diogo L, Grazina M, Garcia P, Ataíde A, Marques C, Miguel T, Borges L, Vicente AM, Oliveira CR.

Dev Med Child Neurol. 2005 Mar;47(3):185-9.

PMID:
15739723
12.

Neuropathology of white matter disease in Leber's hereditary optic neuropathy.

Kovács GG, Höftberger R, Majtényi K, Horváth R, Barsi P, Komoly S, Lassmann H, Budka H, Jakab G.

Brain. 2005 Jan;128(Pt 1):35-41. Epub 2004 Oct 13.

PMID:
15483043
13.

Mitochondrial DNA abnormalities and autistic spectrum disorders.

Pons R, Andreu AL, Checcarelli N, Vilà MR, Engelstad K, Sue CM, Shungu D, Haggerty R, de Vivo DC, DiMauro S.

J Pediatr. 2004 Jan;144(1):81-5.

PMID:
14722523
14.

Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease.

van der Walt JM, Nicodemus KK, Martin ER, Scott WK, Nance MA, Watts RL, Hubble JP, Haines JL, Koller WC, Lyons K, Pahwa R, Stern MB, Colcher A, Hiner BC, Jankovic J, Ondo WG, Allen FH Jr, Goetz CG, Small GW, Mastaglia F, Stajich JM, McLaurin AC, Middleton LT, Scott BL, Schmechel DE, Pericak-Vance MA, Vance JM.

Am J Hum Genet. 2003 Apr;72(4):804-11. Epub 2003 Feb 28.

15.
16.

White matter abnormalities in Leber's hereditary optic neuropathy due to the 3460 mitochondrial DNA mutation.

Lev D, Yanoov-Sharav M, Watemberg N, Leshinsky-Silver E, Lerman-Sagie T.

Eur J Paediatr Neurol. 2002;6(2):121-3.

PMID:
11995959
17.

Prospective study of multiple sclerosis with early onset.

Ghezzi A, Pozzilli C, Liguori M, Marrosu MG, Milani N, Milanese C, Simone I, Zaffaroni M.

Mult Scler. 2002 Apr;8(2):115-8.

PMID:
11990867
18.

Mitochondrial DNA mutations in human disease.

DiMauro S, Schon EA.

Am J Med Genet. 2001 Spring;106(1):18-26. Review.

PMID:
11579421
19.

Mitochondrial mutations of Leber's hereditary optic neuropathy: a risk factor for multiple sclerosis.

Vanopdenbosch L, Dubois B, D'Hooghe MB, Meire F, Carton H.

J Neurol. 2000 Jul;247(7):535-43.

PMID:
10993496
20.

Oxidative damage to mitochondrial DNA and activity of mitochondrial enzymes in chronic active lesions of multiple sclerosis.

Lu F, Selak M, O'Connor J, Croul S, Lorenzana C, Butunoi C, Kalman B.

J Neurol Sci. 2000 Aug 15;177(2):95-103.

PMID:
10980305

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