130 related articles for article (PubMed ID: 36729003)
1. KEARNS-SAYRE SYNDROME MASQUERADING AS MYASTHENIA GRAVIS.
Sokol JT; Hoyek S; Fulton AB; Patel NA
Retin Cases Brief Rep; 2024 May; 18(3):396-399. PubMed ID: 36729003
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. [Kearns-Sayre syndrome: ophthalmic manifestations].
Bande Rodriguez M; Pose Bazarra S; Treus Suarez A; Abraldes Lopez-Veiga M; Fernandez Rodriguez MI; Rodriguez Cid MJ
An Pediatr (Barc); 2015 Jan; 82(1):e151-3. PubMed ID: 25441208
[TBL] [Abstract][Full Text] [Related]
5. Unusual clinical presentation of a patient carrying a novel single 1.8 kb deletion of mitochondrial DNA.
Zoccolella S; Torraco A; Amati A; Lamberti P; Serlenga L; Papa S; Petruzzella V
Funct Neurol; 2006; 21(1):39-41. PubMed ID: 16735000
[TBL] [Abstract][Full Text] [Related]
6. Mitochondrial DNA deletion and duplication in Kearns-Sayre Syndrome (KSS) with initial presentation as Pearson Marrow-Pancreas Syndrome (PMPS): Two case reports in Barranquilla, Colombia.
Sabella-Jiménez V; Otero-Herrera C; Silvera-Redondo C; Garavito-Galofre P
Mol Genet Genomic Med; 2020 Nov; 8(11):e1509. PubMed ID: 33030289
[TBL] [Abstract][Full Text] [Related]
7. [Kearns-Sayre syndrome: a case report].
Gaboune L; Baha Ali T; Benfdil N; Khoumiri R; Ouaggag B; Sayouti A; Moutaouakil A
J Fr Ophtalmol; 2012 Nov; 35(9):718.e1-4. PubMed ID: 22981519
[TBL] [Abstract][Full Text] [Related]
8. Ophthalmologic school-based screening revealing Kearns-Sayre syndrome: a case report.
Ennejjar A; Moutamani S; Boutaj T; Touil W; Amazouzi A; Cherkaoui O
Pan Afr Med J; 2022; 41():226. PubMed ID: 35721635
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Kearns-Sayre syndrome with a novel large-scale deletion: a case report.
Zhu Q; Chen C; Yao J
BMC Ophthalmol; 2022 Jan; 22(1):35. PubMed ID: 35073857
[TBL] [Abstract][Full Text] [Related]
11. Potpourri of retinopathies in rare eye disease - A case series.
Pawar N; Manayath GJ; Verghese S; Chandrakanth P; Shah V; Raut A; Gaikwad S; Patil PA; Daswani M; Meenakshi R; Narendran K; Narendran V
Indian J Ophthalmol; 2022 Jul; 70(7):2605-2609. PubMed ID: 35791168
[TBL] [Abstract][Full Text] [Related]
12. A report on a rare case of Kearns Sayre-like syndrome.
Gupta Y; Gupta M; Sambhav K; Phougat A; Varshney A
Nepal J Ophthalmol; 2010; 2(2):160-3. PubMed ID: 21505535
[TBL] [Abstract][Full Text] [Related]
13. [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]
14. Kearns-Sayre syndrome: a case report and review.
Gross-Jendroska M; Schatz H; McDonald HR; Johnson RN
Eur J Ophthalmol; 1992; 2(1):15-20. PubMed ID: 1638160
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Mitochondrial DNA deletion with Kearns Sayre syndrome in a child with Addison disease.
Boles RG; Roe T; Senadheera D; Mahnovski V; Wong LJ
Eur J Pediatr; 1998 Aug; 157(8):643-7. PubMed ID: 9727847
[TBL] [Abstract][Full Text] [Related]
17. Exophthalmos in Kearns-Sayre syndrome.
Tauber J; Polla DJ; Park S
J AAPOS; 2019 Oct; 23(5):295-297. PubMed ID: 31158487
[TBL] [Abstract][Full Text] [Related]
18. [A case of Kearns-Sayre syndrome].
Kokot W; Iwaszkiewicz-Bilikiewiczowa B; Lewczuk A; Sworczak K
Klin Oczna; 1996; 98(4):327-30. PubMed ID: 9463130
[TBL] [Abstract][Full Text] [Related]
19. [Chronic progressive external ophthalmoplegia and Kearns-Sayre syndrome : interdisciplinary diagnosis and therapy].
Wabbels B; Ali N; Kunz WS; Roggenkämper P; Kornblum C
Ophthalmologe; 2008 Jun; 105(6):550-6. PubMed ID: 18373100
[TBL] [Abstract][Full Text] [Related]
20. Myasthenic symptoms in patients with mitochondrial myopathies.
Le Forestier N; Gherardi RK; Meyrignac C; Annane D; Marsac C; Gray F; Gajdos P
Muscle Nerve; 1995 Nov; 18(11):1338-40. PubMed ID: 7565935
[No Abstract] [Full Text] [Related]
[Next] [New Search]