These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
106 related articles for article (PubMed ID: 8689794)
21. Diagnostic yield muscle biopsy in patients with clinical evidence of mitochondrial cytopathy. Rollins S; Prayson RA; McMahon JT; Cohen BH Am J Clin Pathol; 2001 Sep; 116(3):326-30. PubMed ID: 11554158 [TBL] [Abstract][Full Text] [Related]
22. Increase of mitochondria in vasa nervorum of cases with mitochondrial myopathy, Kearns-Sayre syndrome, progressive external ophthalmoplegia and MELAS. Molnar M; Neudecker S; Schröder JM Neuropathol Appl Neurobiol; 1995 Oct; 21(5):432-9. PubMed ID: 8632838 [TBL] [Abstract][Full Text] [Related]
23. Mitochondrial disorder, diabetes mellitus, and findings in three muscles, including the heart. Venugopal B; Wong KT; Goto YI; Bhattacharjee MB Ultrastruct Pathol; 2006; 30(3):135-41. PubMed ID: 16825114 [TBL] [Abstract][Full Text] [Related]
24. [Diagnostic value of mitochondrial DNA analysis in chronic progressive external ophthalmoplegia (CPEO)]. Kornblum C; Kunz WS; Klockgether T; Roggenkämper P; Schröder R Klin Monbl Augenheilkd; 2004 Dec; 221(12):1057-61. PubMed ID: 15599814 [TBL] [Abstract][Full Text] [Related]
25. Different mitochondrial genetic defects exhibit the same protein signature of metabolism in skeletal muscle of PEO and MELAS patients: A role for oxidative stress. Santacatterina F; Torresano L; Núñez-Salgado A; Esparza-Molto PB; Olive M; Gallardo E; García-Arumi E; Blazquez A; González-Quintana A; Martín MA; Cuezva JM Free Radic Biol Med; 2018 Oct; 126():235-248. PubMed ID: 30138712 [TBL] [Abstract][Full Text] [Related]
26. A novel mutation in the mitochondrial DNA tRNA Leu (UUR) gene associated with late-onset ocular myopathy. Maeso E; Rueda A; Jiménez S; Del Hoyo P; Martín R; Cabello A; Mendoza LM; Arenas J; Campos Y Neuromuscul Disord; 2007 May; 17(5):415-8. PubMed ID: 17363246 [TBL] [Abstract][Full Text] [Related]
27. An infant with a mitochondrial A3243G mutation demonstrating the MELAS phenotype. Kanaumi T; Hirose S; Goto Y; Naitou E; Mitsudome A Pediatr Neurol; 2006 Mar; 34(3):235-8. PubMed ID: 16504796 [TBL] [Abstract][Full Text] [Related]
28. Antioxidant agents have a different expression pattern in muscle fibers of patients with mitochondrial diseases. Filosto M; Tonin P; Vattemi G; Spagnolo M; Rizzuto N; Tomelleri G Acta Neuropathol; 2002 Mar; 103(3):215-20. PubMed ID: 11907800 [TBL] [Abstract][Full Text] [Related]
29. [Mitochondrial myopathy and mitochondrial encephalomyopathy]. Song D; Liu C; Lu Q; Shi J; Chen J; Zhang H; Zhang Y; Wang H; Zhang W; Li G Zhonghua Yi Xue Za Zhi; 2002 Feb; 82(3):158-60. PubMed ID: 11953149 [TBL] [Abstract][Full Text] [Related]
30. Oxidative capacity correlates with muscle mutation load in mitochondrial myopathy. Jeppesen TD; Schwartz M; Olsen DB; Vissing J Ann Neurol; 2003 Jul; 54(1):86-92. PubMed ID: 12838523 [TBL] [Abstract][Full Text] [Related]
31. Immunohistochemical study of heat shock proteins 27, 60 and 70 in the normal human adrenal and in adrenal tumors with suppressed ACTH production. Pignatelli D; Ferreira J; Soares P; Costa MJ; Magalhães MC Microsc Res Tech; 2003 Jun; 61(3):315-23. PubMed ID: 12768547 [TBL] [Abstract][Full Text] [Related]
32. Clinical, pathologic and genetic studies on mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes. Guo Y; Guo Z; Chen L; Zhang J; Wang W; Liu X; Ren H; Gao S Chin Med J (Engl); 1997 Nov; 110(11):851-5. PubMed ID: 9772417 [TBL] [Abstract][Full Text] [Related]
33. Neurotrophin-4 is up-regulated in ragged-red fibers associated with pathogenic mitochondrial DNA mutations. Walker UA; Schon EA Ann Neurol; 1998 Apr; 43(4):536-40. PubMed ID: 9546339 [TBL] [Abstract][Full Text] [Related]
34. Cerebral blood flow and glucose metabolism in mitochondrial disorders. Molnár MJ; Valikovics A; Molnár S; Trón L; Diószeghy P; Mechler F; Gulyás B Neurology; 2000 Aug; 55(4):544-8. PubMed ID: 10953189 [TBL] [Abstract][Full Text] [Related]
35. Immunohistochemical analysis of the oxidative phosphorylation complexes in skeletal muscle from patients with mitochondrial DNA encoded tRNA gene defects. De Paepe B; Smet J; Lammens M; Seneca S; Martin JJ; De Bleecker J; De Meirleir L; Lissens W; Van Coster R J Clin Pathol; 2009 Feb; 62(2):172-6. PubMed ID: 19181635 [TBL] [Abstract][Full Text] [Related]
36. [Clinical characteristics and ultra-structural features of skeletal muscle in mitochondrial cytopathies]. Zhang ZQ; Sun YL; Niu ST; Liang XH; Wang YJ Zhonghua Yi Xue Za Zhi; 2009 May; 89(17):1185-8. PubMed ID: 19595083 [TBL] [Abstract][Full Text] [Related]
37. Oculopharyngeal somatic myopathy in a patient with a novel large-scale 3,399 bp deletion and a homoplasmic T5814C transition of the mitochondrial DNA. Thajeb P; Ma YS; Tzen CY; Chuang CK; Wu TY; Chen SC; Wei YH Clin Neurol Neurosurg; 2006 Jun; 108(4):407-10. PubMed ID: 16644408 [TBL] [Abstract][Full Text] [Related]
39. Characterization and cellular distribution of heat-shock proteins HSP70 and HSP60 in Trypanosoma cruzi. Giambiagi-deMarval M; Souto-Padrón T; Rondinelli E Exp Parasitol; 1996 Aug; 83(3):335-45. PubMed ID: 8823250 [TBL] [Abstract][Full Text] [Related]
40. mtDNA deletion in a patient with symptoms of mitochondrial cytopathy but without ragged red fibers. Blok RB; Thorburn DR; Danks DM; Dahl HH Biochem Mol Med; 1995 Oct; 56(1):26-30. PubMed ID: 8593534 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]