202 related articles for article (PubMed ID: 10437772)
21. Mitochondrial diseases.
Rozwodowska M; Drewa G; Zbytniewski Z; Woźniak A; Krzyzyńska-Malinowska E; Maciak R
Med Sci Monit; 2000; 6(4):817-22. PubMed ID: 11208416
[TBL] [Abstract][Full Text] [Related]
22. Mitochondrial genetics and disease.
Schon EA
Trends Biochem Sci; 2000 Nov; 25(11):555-60. PubMed ID: 11084368
[TBL] [Abstract][Full Text] [Related]
23. Mitochondrial disorders.
Moraes CT
Curr Opin Neurol; 1996 Oct; 9(5):369-74. PubMed ID: 8894413
[TBL] [Abstract][Full Text] [Related]
24. Mitochondrial defects and hearing loss.
Hutchin TP; Cortopassi GA
Cell Mol Life Sci; 2000 Dec; 57(13-14):1927-37. PubMed ID: 11215518
[TBL] [Abstract][Full Text] [Related]
25. Gene therapy by mitochondrial transfer.
Kagawa Y; Inoki Y; Endo H
Adv Drug Deliv Rev; 2001 Jul; 49(1-2):107-19. PubMed ID: 11377806
[TBL] [Abstract][Full Text] [Related]
26. Mitochondrial myopathies in adults and children: management and therapy development.
Pitceathly RD; McFarland R
Curr Opin Neurol; 2014 Oct; 27(5):576-82. PubMed ID: 25188013
[TBL] [Abstract][Full Text] [Related]
27. The genetics and pathology of oxidative phosphorylation.
Smeitink J; van den Heuvel L; DiMauro S
Nat Rev Genet; 2001 May; 2(5):342-52. PubMed ID: 11331900
[TBL] [Abstract][Full Text] [Related]
28. Mitochondrial DNA in aging and degenerative disease.
Berdanier CD; Everts HB
Mutat Res; 2001 Apr; 475(1-2):169-83. PubMed ID: 11295162
[TBL] [Abstract][Full Text] [Related]
29. [Mitochondrial medicine: human chromosome 25 and mitochondrial diseases].
Walker UA
Dtsch Med Wochenschr; 1999 Feb; 124(7):189-92. PubMed ID: 10093578
[No Abstract] [Full Text] [Related]
30. Mitochondrial DNA alterations as a source of human disorders.
Tritschler HJ; Medori R
Neurology; 1993 Feb; 43(2):280-8. PubMed ID: 8437690
[TBL] [Abstract][Full Text] [Related]
31. [Diseases of mitochondrial DNA].
Montoya J; Playán A; Solano A; Alcaine MJ; López-Pérez MJ; Pérez-Martos A
Rev Neurol; 2000 Aug 16-31; 31(4):324-33. PubMed ID: 11008288
[TBL] [Abstract][Full Text] [Related]
32. [Mitochondrial diseases].
Schaefer J; Reichmann H
Dtsch Med Wochenschr; 2001 Aug; 126(33):913-7. PubMed ID: 11514927
[No Abstract] [Full Text] [Related]
33. Approaches to mitochondrial gene therapy.
D'Souza GG; Weissig V
Curr Gene Ther; 2004 Sep; 4(3):317-28. PubMed ID: 15384945
[TBL] [Abstract][Full Text] [Related]
34. Pathogenesis and treatment of mitochondrial myopathies: recent advances.
DiMauro S
Acta Myol; 2010 Oct; 29(2):333-8. PubMed ID: 21314015
[TBL] [Abstract][Full Text] [Related]
35. The universality of bioenergetic disease: the role of mitochondrial mutation and the putative inter-relationship between mitochondria and plasma membrane NADH oxidoreductase.
Lawen A; Martinus RD; McMullen GL; Nagley P; Vaillant F; Wolvetang EJ; Linnane AW
Mol Aspects Med; 1994; 15 Suppl():s13-27. PubMed ID: 7752823
[No Abstract] [Full Text] [Related]
36. Mitochondria take center stage in aging and neurodegeneration.
Beal MF
Ann Neurol; 2005 Oct; 58(4):495-505. PubMed ID: 16178023
[TBL] [Abstract][Full Text] [Related]
37. Mitochondrial cytopathies.
Schmiedel J; Jackson S; Schäfer J; Reichmann H
J Neurol; 2003 Mar; 250(3):267-77. PubMed ID: 12638015
[TBL] [Abstract][Full Text] [Related]
38. Mechanism of somatic mitochondrial DNA mutations associated with age and diseases.
Ozawa T
Biochim Biophys Acta; 1995 May; 1271(1):177-89. PubMed ID: 7599206
[TBL] [Abstract][Full Text] [Related]
39. Mitochondrial dynamics and aging: Mitochondrial interaction preventing individuals from expression of respiratory deficiency caused by mutant mtDNA.
Sato A; Nakada K; Hayashi J
Biochim Biophys Acta; 2006; 1763(5-6):473-81. PubMed ID: 16624428
[TBL] [Abstract][Full Text] [Related]
40. Clinical mitochondrial genetics.
Chinnery PF; Howell N; Andrews RM; Turnbull DM
J Med Genet; 1999 Jun; 36(6):425-36. PubMed ID: 10874629
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]