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 *

117 related articles for article (PubMed ID: 9139281)

  • 1. [Kearns-Sayre syndrome: encephalomyopathy caused by deletion of mitochondrial DNA].
    Lewczuk A; Sworczak K; Falkiewicz B
    Pol Arch Med Wewn; 1996 Dec; 96(6):597-604. PubMed ID: 9139281
    [No Abstract]   [Full Text] [Related]  

  • 2. Kearns-Sayre syndrome with a phenocopy of choroideremia instead of pigmentary retinopathy.
    Herzberg NH; van Schooneveld MJ; Bleeker-Wagemakers EM; Zwart R; Cremers FP; van der Knaap MS; Bolhuis PA; de Visser M
    Neurology; 1993 Jan; 43(1):218-21. PubMed ID: 8423892
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Kearns-Sayre syndrome case presenting a mitochondrial DNA deletion with unusual direct repeats and a rudimentary RNAase mitochondrial ribonucleotide processing target sequence.
    Remes AM; Peuhkurinen KJ; Herva R; Majamaa K; Hassinen IE
    Genomics; 1993 Apr; 16(1):256-8. PubMed ID: 7683627
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Histological, enzymatic and mitochondrial DNA studies in patients with Kearns-Sayre syndrome and chronic progressive external ophthalmoplegia.
    Reichmann H; Degoul F; Gold R; Meurers B; Ketelsen UP; Hartmann J; Marsac C; Lestienne P
    Eur Neurol; 1991; 31(2):108-13. PubMed ID: 1646110
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Corneal decompensation in a boy with Kearns-Sayre syndrome.
    Boonstra F; Claerhout I; Hol F; Smit G; van Collenburg J; Meire F
    Ophthalmic Genet; 2002 Dec; 23(4):247-51. PubMed ID: 12567267
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Kearns-Sayre syndrome: different amounts of deleted mitochondrial DNA are present in several autoptic tissues.
    Ponzetto C; Bresolin N; Bordoni A; Moggio M; Meola G; Bet L; Prelle A; Scarlato G
    J Neurol Sci; 1990 May; 96(2-3):207-10. PubMed ID: 2376752
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The clinical diagnosis and molecular genetics of kearns-sayre syndrome: a complex mitochondrial encephalomyopathy.
    Maceluch JA; Niedziela M
    Pediatr Endocrinol Rev; 2006 Dec-2007 Jan; 4(2):117-37. PubMed ID: 17342029
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Quantification of mitochondrial DNA in heteroplasmic fibroblasts with competitive PCR.
    Wang H; Fliegel L; Cass CE; Penn AM; Michalak M; Weiner JH; Lemire BD
    Biotechniques; 1994 Jul; 17(1):76-8, 80, 82. PubMed ID: 7946321
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Macular lesion resembling adult-onset vitelliform macular dystrophy in Kearns-Sayre syndrome with multiple mtDNA deletions.
    Ascaso FJ; Lopez-Gallardo E; Del Prado E; Ruiz-Pesini E; Montoya J
    Clin Exp Ophthalmol; 2010 Nov; 38(8):812-6. PubMed ID: 20497429
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A case of Kearns-Sayre syndrome with the 4,977-bp common deletion associated with a novel 7,704-bp deletion.
    Vázquez-Acevedo M; Vázquez-Memije ME; Mutchinick OM; Morales JJ; García-Ramos G; González-Halphen D
    Neurol Sci; 2002 Dec; 23(5):247-50. PubMed ID: 12522683
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mitochondrial cytochrome b gene deletion in Kearns-Sayre syndrome associated with a subclinical type of peripheral neuropathy.
    Zanssen S; Molnar M; Buse G; Schröder JM
    Clin Neuropathol; 1998; 17(6):291-6. PubMed ID: 9832255
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Kearns-Sayre syndrome in the absence of a mtDNA deletion?
    Finsterer J; Zarrouk-Mahjoub S
    Andrologia; 2017 Dec; 49(10):. PubMed ID: 29124809
    [No Abstract]   [Full Text] [Related]  

  • 17. Characterization of a 5025 base pair mitochondrial DNA deletion in Kearns-Sayre syndrome.
    Vázquez-Acevedo M; Coria R; González-Astiazarán A; Medina-Crespo V; Ridaura-Sanz C; González-Halphen D
    Biochim Biophys Acta; 1995 Jun; 1271(2-3):363-8. PubMed ID: 7605803
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [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]  

  • 19. [Kearns-Sayre syndrome].
    Berio A; Piazzi A
    Pediatr Med Chir; 2005; 27(3-4):64-9. PubMed ID: 16910453
    [No Abstract]   [Full Text] [Related]  

  • 20. Pernicious anaemia and hypoparathyroidism in a patient with Kearns-Sayre syndrome with mitochondrial DNA duplication.
    Abramowicz MJ; Cochaux P; Cohen LH; Vamos E
    J Inherit Metab Dis; 1996; 19(2):109-11. PubMed ID: 8739941
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.