103 related articles for article (PubMed ID: 8139599)
21. Iron-dependent enzymes in Parkinson's disease.
Reichmann H; Janetzky B; Riederer P
J Neural Transm Suppl; 1995; 46():157-64. PubMed ID: 8821051
[TBL] [Abstract][Full Text] [Related]
22. Biochemical analysis of cybrids expressing mitochondrial DNA from Contursi kindred Parkinson's subjects.
Swerdlow RH; Parks JK; Cassarino DS; Binder DR; Bennett JP; Di Iorio G; Golbe LI; Parker WD
Exp Neurol; 2001 Jun; 169(2):479-85. PubMed ID: 11358461
[TBL] [Abstract][Full Text] [Related]
23. High frequency of mitochondrial complex I mutations in Parkinson's disease and aging.
Smigrodzki R; Parks J; Parker WD
Neurobiol Aging; 2004; 25(10):1273-81. PubMed ID: 15465623
[TBL] [Abstract][Full Text] [Related]
24. Role of genetics in the cause of Parkinson's disease.
Duvoisin RC
Mov Disord; 1998; 13 Suppl 1():7-12. PubMed ID: 9613712
[No Abstract] [Full Text] [Related]
25. Mitochondrial genotypes and cytochrome b variants associated with longevity or Parkinson's disease.
Tanaka M
J Neurol; 2002 Sep; 249 Suppl 2():II11-8. PubMed ID: 12375058
[TBL] [Abstract][Full Text] [Related]
26. Genetic and environmental factors in Parkinson's disease.
Duvoisin RC
Adv Neurol; 1999; 80():161-3. PubMed ID: 10410716
[No Abstract] [Full Text] [Related]
27. Study of platelet alpha 2-adrenoceptors in Parkinson's disease.
Montastruc JL; Villeneuve A; Berlan M; Lafontan M; Caranobe C; Boneu B; Rascol A
Adv Neurol; 1987; 45():253-8. PubMed ID: 3030069
[No Abstract] [Full Text] [Related]
28. Parkinson's disease and the electron transport chain in postmortem brain.
Reichmann H; Lestienne P; Jellinger K; Riederer P
Adv Neurol; 1993; 60():297-9. PubMed ID: 8380522
[No Abstract] [Full Text] [Related]
29. Presymptomatic detection of Parkinson's disease.
Jenner P
J Neural Transm Suppl; 1993; 40():23-36. PubMed ID: 8294898
[TBL] [Abstract][Full Text] [Related]
30. Mitochondrial complex I, II/III, and IV activities in familial and sporadic Parkinson's disease.
Hanagasi HA; Ayribas D; Baysal K; Emre M
Int J Neurosci; 2005 Apr; 115(4):479-93. PubMed ID: 15809215
[TBL] [Abstract][Full Text] [Related]
31. Nuclear DNA origin of mitochondrial complex I deficiency in fatal infantile lactic acidosis evidenced by transnuclear complementation of cultured fibroblasts.
Procaccio V; Mousson B; Beugnot R; Duborjal H; Feillet F; Putet G; Pignot-Paintrand I; Lombès A; De Coo R; Smeets H; Lunardi J; Issartel JP
J Clin Invest; 1999 Jul; 104(1):83-92. PubMed ID: 10393702
[TBL] [Abstract][Full Text] [Related]
32. Novel mitochondrial DNA deletion found in a renal cell carcinoma.
Horton TM; Petros JA; Heddi A; Shoffner J; Kaufman AE; Graham SD; Gramlich T; Wallace DC
Genes Chromosomes Cancer; 1996 Feb; 15(2):95-101. PubMed ID: 8834172
[TBL] [Abstract][Full Text] [Related]
33. Detrimental deletions: mitochondria, aging and Parkinson's disease.
Biskup S; Moore DJ
Bioessays; 2006 Oct; 28(10):963-7. PubMed ID: 16998822
[TBL] [Abstract][Full Text] [Related]
34. Golden mean to longevity: rareness of mitochondrial cytochrome b variants in centenarians but not in patients with Parkinson's disease.
Tanaka M; Fuku N; Takeyasu T; Guo LJ; Hirose R; Kurata M; Borgeld HJ; Yamada Y; Maruyama W; Arai Y; Hirose N; Oshida Y; Sato Y; Hattori N; Mizuno Y; Iwata S; Yagi K
J Neurosci Res; 2002 Nov; 70(3):347-55. PubMed ID: 12391595
[TBL] [Abstract][Full Text] [Related]
35. Reduced NADH coenzyme Q dehydrogenase activity in platelets of Parkinson's disease, but not Parkinson plus patients, from an Indian population.
Varghese M; Pandey M; Samanta A; Gangopadhyay PK; Mohanakumar KP
J Neurol Sci; 2009 Apr; 279(1-2):39-42. PubMed ID: 19176229
[TBL] [Abstract][Full Text] [Related]
36. Cytoplasmic transfer of platelet mtDNA from elderly patients with Parkinson's disease to mtDNA-less HeLa cells restores complete mitochondrial respiratory function.
Aomi Y; Chen CS; Nakada K; Ito S; Isobe K; Murakami H; Kuno SY; Tawata M; Matsuoka R; Mizusawa H; Hayashi JI
Biochem Biophys Res Commun; 2001 Jan; 280(1):265-73. PubMed ID: 11162509
[TBL] [Abstract][Full Text] [Related]
37. Mitochondrial polymporphisms in Parkinson's Disease.
Otaegui D; Paisán C; Sáenz A; Martí I; Ribate M; Martí-Massó JF; Pérez-Tur J; López de Munain A
Neurosci Lett; 2004 Nov; 370(2-3):171-4. PubMed ID: 15488317
[TBL] [Abstract][Full Text] [Related]
38. A mitochondrial etiology of neurodegenerative diseases: evidence from Parkinson's disease.
Khusnutdinova E; Gilyazova I; Ruiz-Pesini E; Derbeneva O; Khusainova R; Khidiyatova I; Magzhanov R; Wallace DC
Ann N Y Acad Sci; 2008 Dec; 1147():1-20. PubMed ID: 19076426
[TBL] [Abstract][Full Text] [Related]
39. Wolfram (DIDMOAD) syndrome and Leber hereditary optic neuropathy (LHON) are associated with distinct mitochondrial DNA haplotypes.
Hofmann S; Bezold R; Jaksch M; Obermaier-Kusser B; Mertens S; Kaufhold P; Rabl W; Hecker W; Gerbitz KD
Genomics; 1997 Jan; 39(1):8-18. PubMed ID: 9027481
[TBL] [Abstract][Full Text] [Related]
40. Genetic polymorphisms in Parkinson's disease.
Checkoway H; Farin FM; Costa-Mallen P; Kirchner SC; Costa LG
Neurotoxicology; 1998; 19(4-5):635-43. PubMed ID: 9745923
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]