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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

150 related articles for article (PubMed ID: 1289103)

  • 1. 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]  

  • 2. Mitochondrial DNA deletion diagnosed by analysis of an endomyocardial biopsy specimen from a patient with Kearns-Sayre syndrome and complete heart block.
    Remes AM; Hassinen IE; Majamaa K; Peuhkurinen KJ
    Br Heart J; 1992 Oct; 68(4):408-11. PubMed ID: 1449926
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cardiac transplantation in an incomplete Kearns-Sayre syndrome with mitochondrial DNA deletion.
    Tranchant C; Mousson B; Mohr M; Dumoulin R; Welsch M; Weess C; Stepien G; Warter JM
    Neuromuscul Disord; 1993; 3(5-6):561-6. PubMed ID: 8186712
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Kearns-Sayre syndrome with muscle mitochondrial DNA deletion.
    Lestienne P; Ponsot G
    Lancet; 1988 Apr; 1(8590):885. PubMed ID: 2895391
    [No Abstract]   [Full Text] [Related]  

  • 5. [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]  

  • 6. [PCR-based detection of heteroplasmic deleted mitochondrial DNA in Kearns-Sayre syndrome].
    Ramírez-Miranda A; Navas-Pérez A; Gurria-Quintana L; Vargas-Ortega J; Murillo-Correa C; Zenteno JC
    Arch Soc Esp Oftalmol; 2008 Mar; 83(3):155-9. PubMed ID: 18311673
    [TBL] [Abstract][Full Text] [Related]  

  • 7. mtDNA deletions in Kearns-Sayre.
    Johns DR
    Neurology; 1990 Aug; 40(8):1322-3. PubMed ID: 2381550
    [No Abstract]   [Full Text] [Related]  

  • 8. Kearns-Sayre syndrome with a novel mitochondrial DNA deletion.
    Marin-Garcia J; Goldenthal MJ; Sarnat HB
    J Child Neurol; 2000 Aug; 15(8):555-8. PubMed ID: 10961796
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mapping of heteroplasmic mitochondrial DNA deletions in Kearns-Sayre syndrome.
    Nelson I; Degoul F; Obermaier-Kusser B; Romero N; Borrone C; Marsac C; Vayssiere JL; Gerbitz K; Fardeau M; Ponsot G; Lestienne P
    Nucleic Acids Res; 1989 Oct; 17(20):8117-24. PubMed ID: 2813058
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Detection of deletions in platelet mitochondrial DNA in Kearns-Sayre syndrome using polymerase chain reaction].
    Ota Y; Awaya S; Tanaka M; Sato W; Ohno K; Yamamoto T; Ozawa T; Ota I
    Nippon Ganka Gakkai Zasshi; 1991 Aug; 95(8):776-82. PubMed ID: 1950835
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndrome.
    Larsson NG; Holme E; Kristiansson B; Oldfors A; Tulinius M
    Pediatr Res; 1990 Aug; 28(2):131-6. PubMed ID: 2395603
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Mitochondrial genome analysis in Kearns-Sayre syndrome.
    Lertrit P; Atchaneeyasakul L; Devahastin V; Saechan V; Sangruchi T; Neungton N; Lekhakula S
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():162-5. PubMed ID: 8629098
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. [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]  

  • 17. In situ hybridization of mitochondrial DNA in the heart of a patient with Kearns-Sayre syndrome and dilatative cardiomyopathy.
    Müller-Höcker J; Seibel P; Schneiderbanger K; Zietz C; Obermaier-Kusser B; Gerbitz KD; Kadenbach B
    Hum Pathol; 1992 Dec; 23(12):1431-7. PubMed ID: 1334946
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. The common 4977 base pair deletion of mitochondrial DNA preferentially accumulates in the cardiac conduction system of patients with Kearns-Sayre syndrome.
    Müller-Höcker J; Jacob U; Seibel P
    Mod Pathol; 1998 Mar; 11(3):295-301. PubMed ID: 9521479
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Ophthalmoplegia-plus: clinical variability, biochemical defects of the mitochondria respiratory chain and deletions of the mitochondria genome].
    Zierz S; von Wersebe O; Gerbitz KD; Jerusalem F
    Nervenarzt; 1990 Jun; 61(6):332-9. PubMed ID: 2377259
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.