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.
22. [A case of Kearns-Sayre-Shy syndrome with abnormal signal intensity on MRI in cerebral white matter and brainstem]. Shindo K; Tsunoda S; Shiozawa Z Rinsho Shinkeigaku; 1991 May; 31(5):539-42. PubMed ID: 1934767 [TBL] [Abstract][Full Text] [Related]
23. Multiple muscle cell alterations in a case of encephalomyopathy. Fujioka H; Tandler B; Rosca M; McCandless SE; Katirji B; Cohen ML; Rapisuwon S; Hoppel CL Ultrastruct Pathol; 2014 Feb; 38(1):13-25. PubMed ID: 24134831 [TBL] [Abstract][Full Text] [Related]
24. Progression in a case of Kearns-Sayre syndrome. Ishikawa Y; Goto Y; Ishikawa Y; Minami R J Child Neurol; 2000 Nov; 15(11):750-5. PubMed ID: 11108509 [TBL] [Abstract][Full Text] [Related]
25. Kearns-Sayre syndrome -3 case reports and review of clinical feature. Park SB; Ma KT; Kook KH; Lee SY Yonsei Med J; 2004 Aug; 45(4):727-35. PubMed ID: 15344217 [TBL] [Abstract][Full Text] [Related]
26. Mitochondrial encephalomyopathy (Kearns-Sayre syndrome) with complete atrioventricular block: a case report. Kakura H; Tachibana Y; Nakamura K; Tanaka Y; Sanada J; Arima T Jpn Circ J; 1998 Aug; 62(8):623-5. PubMed ID: 9741743 [TBL] [Abstract][Full Text] [Related]
27. Mitochondrial encephalomyopathy: variable clinical expression within a single kindred. Crimmins D; Morris JG; Walker GL; Sue CM; Byrne E; Stevens S; Jean-Francis B; Yiannikas C; Pamphlett R J Neurol Neurosurg Psychiatry; 1993 Aug; 56(8):900-5. PubMed ID: 8350109 [TBL] [Abstract][Full Text] [Related]
28. Deletion of mitochondrial DNA in patients with combined features of Kearns-Sayre and MELAS syndromes. Zupanc ML; Moraes CT; Shanske S; Langman CB; Ciafaloni E; DiMauro S Ann Neurol; 1991 Jun; 29(6):680-3. PubMed ID: 1892371 [TBL] [Abstract][Full Text] [Related]
29. A novel mitochondrial DNA deletion in a Chinese girl with Kearns-Sayre syndrome. Yau EK; Chan KY; Au KM; Chow TC; Chan YW Hong Kong Med J; 2009 Oct; 15(5):374-7. PubMed ID: 19801695 [TBL] [Abstract][Full Text] [Related]
30. [Clinical usefulness of myocardial iodine-123-15-(p-iodophenyl)-3(R,S)-methyl-pentadecanoic acid distribution abnormality in patients with mitochondrial encephalomyopathy based on normal data file in bull's-eye polar map]. Takahashi N; Mitani I; Sumita S; Ashino K; Ishigami T; Ochiai H; Oonishi H; Suzuki Y; Hasegawa O; Ikegami T; Matsubara S; Ishii M J Cardiol; 1998 Jan; 31(1):1-10. PubMed ID: 9488945 [TBL] [Abstract][Full Text] [Related]
31. [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]
32. Mitochondrial encephalomyopathies. Scarlato G; Moggio M; Bet L; Gallanti A; Bresolin N Acta Neurol (Napoli); 1989 Oct; 11(5):322-9. PubMed ID: 2603778 [No Abstract] [Full Text] [Related]
33. A case of Kearns-Sayre syndrome with two novel deletions (9.768 and 7.253 kb) of the mtDNA associated with the common deletion in blood leukocytes, buccal mucosa and hair follicles. Mkaouar-Rebai E; Chamkha I; Kammoun T; Chabchoub I; Aloulou H; Fendri N; Hachicha M; Fakhfakh F Mitochondrion; 2010 Aug; 10(5):449-55. PubMed ID: 20388556 [TBL] [Abstract][Full Text] [Related]
34. [Phenotype heterogeneity associated with mitochondrial DNA A3243G mutation]. Zhang Y; Wang ZX; Niu SL; Xu YF; Pei P; Yuan Y; Yang YL; Qi Y Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2005 Feb; 27(1):77-80. PubMed ID: 15782498 [TBL] [Abstract][Full Text] [Related]