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8. Kearns-Sayre syndrome: different amounts of deleted mitochondrial DNA are present in several autoptic tissues. Ponzetto C; Bresolin N; Bordoni A; Moggio M; Meola G; Bet L; Prelle A; Scarlato G J Neurol Sci; 1990 May; 96(2-3):207-10. PubMed ID: 2376752 [TBL] [Abstract][Full Text] [Related]
9. Neuro-ophthalmologic manifestations of mitochondrial DNA disorders: chronic progressive external ophthalmoplegia, Kearns-Sayre syndrome, and Leber's hereditary optic neuropathy. Kosmorsky G; Johns DR Neurol Clin; 1991 Feb; 9(1):147-61. PubMed ID: 2011107 [No Abstract] [Full Text] [Related]
10. Heteroplasmy of mitochondrial genomes in clonal cultures from patients with Kearns-Sayre syndrome. Moraes CT; Schon EA; DiMauro S; Miranda AF Biochem Biophys Res Commun; 1989 Apr; 160(2):765-71. PubMed ID: 2541710 [TBL] [Abstract][Full Text] [Related]
11. [Familial Kearns syndrome]. Machraoui A; Breviere GM; Rey C; Ghalayini Z; Nuyts JP; Dupuis C Ann Pediatr (Paris); 1985 Oct; 32(8):701-11. PubMed ID: 4073755 [No Abstract] [Full Text] [Related]
12. [A case of Kearns-Sayre like syndrome associated with rimmed vacuoles]. Tanaka K; Yuasa T; Kumamoto T; Fukuhara N; Kondo K Rinsho Shinkeigaku; 1982 Nov; 22(11):1015-20. PubMed ID: 7168932 [No Abstract] [Full Text] [Related]
16. Kearns-Sayre syndrome with muscle mitochondrial DNA deletion. Lestienne P; Ponsot G Lancet; 1988 Apr; 1(8590):885. PubMed ID: 2895391 [No Abstract] [Full Text] [Related]
17. Mitochondrial genome analysis in Kearns-Sayre syndrome. Lertrit P; Atchaneeyasakul L; Devahastin V; Saechan V; Sangruchi T; Neungton N; Lekhakula S Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():162-5. PubMed ID: 8629098 [TBL] [Abstract][Full Text] [Related]
18. Ultrastructural findings in endomyocardial biopsy of patients with Kearns-Sayre syndrome. Schwartzkopff B; Frenzel H; Breithardt G; Deckert M; Lösse B; Toyka KV; Borggrefe M; Hort W J Am Coll Cardiol; 1988 Dec; 12(6):1522-8. PubMed ID: 3192850 [TBL] [Abstract][Full Text] [Related]
19. Congestive heart failure due to mitochondrial cardiomyopathy in Kearns-Sayre syndrome. Kleber FX; Park JW; Hübner G; Johannes A; Pongratz D; König E Klin Wochenschr; 1987 May; 65(10):480-6. PubMed ID: 3599796 [TBL] [Abstract][Full Text] [Related]
20. [A patient with Pearson and Kearns-Sayre syndrome and a common 4.9 Kb deletion of mitochondrial DNA in blood]. Guirado Giménez F; Montoya Villarroya J; Oliván del Cacho MJ; Playán Ariso A; Alcaine Villarroya MJ; Rábano Rodríguez A; Baldellou Vázquez A; López-Pisón J An Esp Pediatr; 1998 Nov; 49(5):510-2. PubMed ID: 9949596 [No Abstract] [Full Text] [Related] [Next] [New Search]