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.
29. [Congestive cardiomyopathy, peripheral neuropathy, abnormal CT findings, neurosensory deafness, cerebellar ataxia and ophthalmoplegia in oculocraniosomatic neuromuscular disease with ragged red fibers]. Yoshida T; Shinohara H; Kanda H; Asato H; Sasaki T; Suga H; Sugano J; Suzuki T; Ishibashi H; Murata K Nihon Naika Gakkai Zasshi; 1983 Apr; 72(4):438-45. PubMed ID: 6310008 [No Abstract] [Full Text] [Related]
30. Cytochrome c oxidase activity in single muscle fibers: assay techniques and diagnostic applications. Johnson MA; Bindoff LA; Turnbull DM Ann Neurol; 1993 Jan; 33(1):28-35. PubMed ID: 8388186 [TBL] [Abstract][Full Text] [Related]
31. [Ptosis as the leading symptom of Kearns-Sayre syndrome. A case report for differential diagnosis of external ophthalmoplegia]. Vock K; Todt H; Fötzsch R; Fischer R Kinderarztl Prax; 1990 Feb; 58(2):93-7. PubMed ID: 2332951 [TBL] [Abstract][Full Text] [Related]
32. Ophthalmoplegia in Mitochondrial Disease. Lee SJ; Na JH; Han J; Lee YM Yonsei Med J; 2018 Dec; 59(10):1190-1196. PubMed ID: 30450853 [TBL] [Abstract][Full Text] [Related]
39. Pigmentary retinopathy in Kearns-Sayre syndrome. Padhy SK; Kumar V; Mandal S BMJ Case Rep; 2018 Oct; 2018():. PubMed ID: 30279266 [No Abstract] [Full Text] [Related]
40. 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] [Previous] [Next] [New Search]