207 related articles for article (PubMed ID: 15827867)
1. Sensorineural hearing loss in patients with chronic progressive external ophthalmoplegia or Kearns-Sayre syndrome.
Kornblum C; Broicher R; Walther E; Herberhold S; Klockgether T; Herberhold C; Schröder R
J Neurol; 2005 Sep; 252(9):1101-7. PubMed ID: 15827867
[TBL] [Abstract][Full Text] [Related]
2. [Mitochondrial DNA mutations in patients with chronic progressive external ophthalmoplegia and Kearns-Sayre syndrome].
Wang ZX; Yuan Y; Gao F; Qi Y; Shen DG; Chen QT
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Aug; 20(4):273-8. PubMed ID: 12903032
[TBL] [Abstract][Full Text] [Related]
3. Progressive sensorineural hearing loss in children with mitochondrial encephalomyopathies.
Zwirner P; Wilichowski E
Laryngoscope; 2001 Mar; 111(3):515-21. PubMed ID: 11224785
[TBL] [Abstract][Full Text] [Related]
4. Executive and visuospatial deficits in patients with chronic progressive external ophthalmoplegia and Kearns-Sayre syndrome.
Bosbach S; Kornblum C; Schröder R; Wagner M
Brain; 2003 May; 126(Pt 5):1231-40. PubMed ID: 12690061
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. The clinical, myopathological, and genetic analysis of 155 Chinese mitochondrial ophthalmoplegia patients with mitochondrial DNA single large deletions.
Zhao Y; Hou Y; Zhao X; Liufu T; Yu M; Zhang W; Xie Z; Zhang VW; Yuan Y; Wang Z
Mol Genet Genomic Med; 2024 Jan; 12(1):e2328. PubMed ID: 38018320
[TBL] [Abstract][Full Text] [Related]
7. [Audiologic features of mitochondrial DNA A3243G mutation and its correlation with mutation rate].
Xue JF; Chen L; Ma YN; Zhao DH; Duan JB; Wang ZX; Qi Y; Liu YH
Zhonghua Yi Xue Za Zhi; 2012 Oct; 92(40):2830-4. PubMed ID: 23290211
[TBL] [Abstract][Full Text] [Related]
8. [Chronic progressive external ophthalmoplegia (CPEO), Kearns-Sayre syndrome (KSS)].
Ishikawa H; Nishino I
Ryoikibetsu Shokogun Shirizu; 2001; (36):153-6. PubMed ID: 11596351
[No Abstract] [Full Text] [Related]
9. Are duplications of mitochondrial DNA characteristic of Kearns-Sayre syndrome?
Poulton J; Morten KJ; Weber K; Brown GK; Bindoff L
Hum Mol Genet; 1994 Jun; 3(6):947-51. PubMed ID: 7951243
[TBL] [Abstract][Full Text] [Related]
10. [Single deletion of mitochondrial DNA: CPEO, Kearns-Sayre syndrome].
Arisato T; Higuchi I; Nakagawa M
Nihon Rinsho; 2002 Apr; 60 Suppl 4():458-61. PubMed ID: 12013912
[No Abstract] [Full Text] [Related]
11. Clinical Phenotype and Genetic Features of a Pair of Chinese Twins with Kearns-Sayre Syndrome.
Guo L; Wang X; Ji H
DNA Cell Biol; 2020 Aug; 39(8):1449-1457. PubMed ID: 32609007
[TBL] [Abstract][Full Text] [Related]
12. A review of cochlear implantation in mitochondrial sensorineural hearing loss.
Sinnathuray AR; Raut V; Awa A; Magee A; Toner JG
Otol Neurotol; 2003 May; 24(3):418-26. PubMed ID: 12806294
[TBL] [Abstract][Full Text] [Related]
13. Audiological evaluation in Chinese patients with mitochondrial encephalomyopathies.
Liu Y; Xue J; Zhao D; Chen L; Yuan Y; Wang Z
Chin Med J (Engl); 2014; 127(12):2304-9. PubMed ID: 24931247
[TBL] [Abstract][Full Text] [Related]
14. [Progressive external ophthalmoplegia and the Kearns-Sayre syndrome: a clinical and molecular study of 6 cases].
Barrientos A; Casademont J; Grau JM; Cardellach F; Montoya J; Estivill X; Urbano-Márquez A; Nunes V
Med Clin (Barc); 1995 Jul; 105(5):180-4. PubMed ID: 7630231
[TBL] [Abstract][Full Text] [Related]
15. Duplications of mitochondrial DNA in Kearns-Sayre syndrome.
Poulton J; Morten KJ; Marchington D; Weber K; Brown GK; Rötig A; Bindoff L
Muscle Nerve Suppl; 1995; 3():S154-8. PubMed ID: 7603518
[TBL] [Abstract][Full Text] [Related]
16. MELAS- and Kearns-Sayre-type co-mutation [corrected] with myopathy and autoimmune polyendocrinopathy.
Ohno K; Yamamoto M; Engel AG; Harper CM; Roberts LR; Tan GH; Fatourechi V
Ann Neurol; 1996 Jun; 39(6):761-6. PubMed ID: 8651648
[TBL] [Abstract][Full Text] [Related]
17. Mitochondrial single-stranded DNA binding protein novel de novo SSBP1 mutation in a child with single large-scale mtDNA deletion (SLSMD) clinically manifesting as Pearson, Kearns-Sayre, and Leigh syndromes.
Gustafson MA; McCormick EM; Perera L; Longley MJ; Bai R; Kong J; Dulik M; Shen L; Goldstein AC; McCormack SE; Laskin BL; Leroy BP; Ortiz-Gonzalez XR; Ellington MG; Copeland WC; Falk MJ
PLoS One; 2019; 14(9):e0221829. PubMed ID: 31479473
[TBL] [Abstract][Full Text] [Related]
18. [Audiological findings and mitochondrial DNA mutation in a large family with matrilineal sensorineural hearing loss].
Xing G; Bu X; Yan M; Lu L; Yang S
Zhonghua Er Bi Yan Hou Ke Za Zhi; 2000 Apr; 35(2):98-101. PubMed ID: 12768662
[TBL] [Abstract][Full Text] [Related]
19. Kearns-Sayre syndrome case. Novel 5,9 kb mtDNA deletion.
Grigalionienė K; Burnytė B; Balkelienė D; Ambrozaitytė L; Utkus A
Mol Genet Genomic Med; 2023 Jan; 11(1):e2059. PubMed ID: 36181358
[TBL] [Abstract][Full Text] [Related]
20. [Partial deletion of mitochondrial DNA in mitochondrial encephalomyopathies].
Wang W; Zhang J; Guo Y; Guo Z; Ren H
Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1997 Aug; 19(4):278-83. PubMed ID: 10453567
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
