165 related articles for article (PubMed ID: 1305030)
1. Kearns-Sayre's syndrome developing in a boy who survived pearson's syndrome caused by mitochondrial DNA deletion.
Simonsz HJ; Bärlocher K; Rötig A
Doc Ophthalmol; 1992; 82(1-2):73-9. PubMed ID: 1305030
[TBL] [Abstract][Full Text] [Related]
2. Deletion in blood mitochondrial DNA in Kearns-Sayre syndrome.
Fischel-Ghodsian N; Bohlman MC; Prezant TR; Graham JM; Cederbaum SD; Edwards MJ
Pediatr Res; 1992 Jun; 31(6):557-60. PubMed ID: 1635816
[TBL] [Abstract][Full Text] [Related]
3. Kearns-Sayre syndrome with features of Pearson's marrow-pancreas syndrome and a novel 2905-base pair mitochondrial DNA deletion.
Becher MW; Wills ML; Noll WW; Hurko O; Price DL
Hum Pathol; 1999 May; 30(5):577-81. PubMed ID: 10333230
[TBL] [Abstract][Full Text] [Related]
4. Kearns-Sayre syndrome presenting as renal tubular acidosis.
Eviatar L; Shanske S; Gauthier B; Abrams C; Maytal J; Slavin M; Valderrama E; DiMauro S
Neurology; 1990 Nov; 40(11):1761-3. PubMed ID: 2234434
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. [Retinitis pigmentosa in Kearns-Sayre syndrome resulting from mutation of mitochondrial DNA "de novo"].
Midro AT; Zalewska R; Skrzypczak-Adamiak G; Wilichowski E
Klin Oczna; 1995 Jun; 97(6):203-6. PubMed ID: 7643565
[TBL] [Abstract][Full Text] [Related]
7. Kearns-Sayre syndrome with sideroblastic anemia: molecular investigations.
Nelson I; Bonne G; Degoul F; Marsac C; Ponsot G; Lestienne P
Neuropediatrics; 1992 Aug; 23(4):199-205. PubMed ID: 1407387
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Combined cyclic vomiting and Kearns-Sayre syndromes.
Boles RG; Baldwin EE; Prezant TR
Pediatr Neurol; 2007 Feb; 36(2):135-6. PubMed ID: 17275670
[TBL] [Abstract][Full Text] [Related]
10. [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]
11. Pearson syndrome and mitochondrial encephalomyopathy in a patient with a deletion of mtDNA.
McShane MA; Hammans SR; Sweeney M; Holt IJ; Beattie TJ; Brett EM; Harding AE
Am J Hum Genet; 1991 Jan; 48(1):39-42. PubMed ID: 1985462
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Mitochondrial DNA deletion in a child with megaloblastic anemia and recurrent encephalopathy.
Akman CI; Sue CM; Shanske S; Tanji K; Bonilla E; Ojaimi J; Krishna S; Schubert R; DiMauro S
J Child Neurol; 2004 Apr; 19(4):258-61. PubMed ID: 15163090
[TBL] [Abstract][Full Text] [Related]
14. Unusual presentation of Kearns-Sayre syndrome in early childhood.
Simaan EM; Mikati MA; Touma EH; Rötig A
Pediatr Neurol; 1999 Nov; 21(5):830-1. PubMed ID: 10593676
[TBL] [Abstract][Full Text] [Related]
15. DEVELOPMENT OF CHRONIC SUBRETINAL FLUID IN KEARNS-SAYRE SYNDROME.
Paulus YM; Wenick AS
Retin Cases Brief Rep; 2016; 10(3):236-8. PubMed ID: 26536013
[TBL] [Abstract][Full Text] [Related]
16. Deletion of mitochondrial DNA in the endomyocardial biopsy sample from a patient with Kearns-Sayre syndrome.
Anan R; Nakagawa M; Higuchi I; Nakao S; Nomoto K; Tanaka H
Eur Heart J; 1992 Dec; 13(12):1718-9. PubMed ID: 1289103
[TBL] [Abstract][Full Text] [Related]
17. [Disorders of mitochondrial energy metabolism in patients with the Kearns-Sayre syndrome].
Capková M; Tesarová M; Wenchich L; Cerná L; Hansíková H; Hůlková H; Hrubá E; Elleder M; Zeman J
Cas Lek Cesk; 2002 Feb; 141(2):51-4. PubMed ID: 11925663
[TBL] [Abstract][Full Text] [Related]
18. Spectrum of mitochondrial DNA rearrangements in the Pearson marrow-pancreas syndrome.
Rötig A; Bourgeron T; Chretien D; Rustin P; Munnich A
Hum Mol Genet; 1995 Aug; 4(8):1327-30. PubMed ID: 7581370
[TBL] [Abstract][Full Text] [Related]
19. Congenital hypoplastic anemia, diabetes, and severe renal tubular dysfunction associated with a mitochondrial DNA deletion.
Majander A; Suomalainen A; Vettenranta K; Sariola H; Perkkiö M; Holmberg C; Pihko H
Pediatr Res; 1991 Oct; 30(4):327-30. PubMed ID: 1956715
[TBL] [Abstract][Full Text] [Related]
20. Kearns-Sayre syndrome "plus". Classical clinical findings and dystonia.
Marie SK; Carvalho AA; Fonseca LF; Carvalho MS; Reed UC; Scaff M
Arq Neuropsiquiatr; 1999 Dec; 57(4):1017-23. PubMed ID: 10683696
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
