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Journal Abstract Search

274 related items for PubMed ID: 9341886

  • 1. Detection and characterization of mitochondrial DNA rearrangements in Pearson and Kearns-Sayre syndromes by long PCR.
    Kleinle S, Wiesmann U, Superti-Furga A, Krähenbühl S, Boltshauser E, Reichen J, Liechti-Gallati S.
    Hum Genet; 1997 Oct; 100(5-6):643-50. PubMed ID: 9341886
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  • 2. 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
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  • 6. 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
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  • 7. High proportions of mtDNA duplications in patients with Kearns-Sayre syndrome occur in the heart.
    Fromenty B, Carrozzo R, Shanske S, Schon EA.
    Am J Med Genet; 1997 Sep 05; 71(4):443-52. PubMed ID: 9286453
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  • 8. A topoisomerase II cleavage site is associated with a novel mitochondrial DNA deletion.
    Blok RB, Thorburn DR, Thompson GN, Dahl HH.
    Hum Genet; 1995 Jan 05; 95(1):75-81. PubMed ID: 7814031
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  • 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 05; 3(6):947-51. PubMed ID: 7951243
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  • 10. 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 Jun 05; 3():S154-8. PubMed ID: 7603518
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  • 11. [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 05; 83(3):155-9. PubMed ID: 18311673
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  • 12. Paediatric single mitochondrial DNA deletion disorders: an overlapping spectrum of disease.
    Broomfield A, Sweeney MG, Woodward CE, Fratter C, Morris AM, Leonard JV, Abulhoul L, Grunewald S, Clayton PT, Hanna MG, Poulton J, Rahman S.
    J Inherit Metab Dis; 2015 May 05; 38(3):445-57. PubMed ID: 25352051
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  • 13. 3.1-kb deletion of mitochondrial DNA in a patient with Kearns-Sayre syndrome.
    Klopstock T, Bischof F, Gerok K, Deuschl G, Seibel P, Ketelsen UP, Reichmann H.
    Acta Neuropathol; 1995 May 05; 90(2):126-9. PubMed ID: 7484086
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  • 14. [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 05; 20(4):273-8. PubMed ID: 12903032
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  • 15. 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 05; 4(8):1327-30. PubMed ID: 7581370
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  • 16. A unique 3.5-kb deletion of the mitochondrial genome in Thai patients with Kearns-Sayre syndrome.
    Lertrit P, Imsumran A, Karnkirawattana P, Devahasdin V, Sangruchi T, Atchaneeyasakul L, Mungkornkarn C, Neungton N.
    Hum Genet; 1999 Aug 05; 105(1-2):127-31. PubMed ID: 10480366
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  • 20. Mitochondrial DNA deletion in human oocytes and embryos.
    Brenner CA, Wolny YM, Barritt JA, Matt DW, Munné S, Cohen J.
    Mol Hum Reprod; 1998 Sep 05; 4(9):887-92. PubMed ID: 9783850
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