BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

676 related articles for article (PubMed ID: 2541333)

  • 21. [Mitochondrial encephalomyopathy].
    Scarlato G; Bresolin N; Moggio M; Bet L; Meola G
    Recenti Prog Med; 1989 Dec; 80(12):665-72. PubMed ID: 2560839
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A case of Kearns-Sayre syndrome with autoimmune thyroiditis and possible Hashimoto encephalopathy.
    Berio A; Piazzi A
    Panminerva Med; 2002 Sep; 44(3):265-9. PubMed ID: 12094144
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Partial deletion of mitochondrial DNA in mitochondrial encephalomyopathies].
    Wang W; Zhang J; Guo Y; Guo Z; Ren H
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1997 Aug; 19(4):278-83. PubMed ID: 10453567
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Ocular mitochondrial myopathies: a spectrum of clinical presentations].
    Glutz von Blotzheim S; Borruat FX; Hirt L
    Klin Monbl Augenheilkd; 1998 May; 212(5):299-300. PubMed ID: 9677561
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. [Nucleotide mapping and a kinetic model of a heteroplasmic deletion of 4,666 base pairs from mitochondrial DNA in the Kearns-Sayre syndrome].
    Nelson I; d'Auriol L; Galibert F; Ponsot G; Lestienne P
    C R Acad Sci III; 1989; 309(10):403-7. PubMed ID: 2514965
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Mitochondrial DNA deletion in a girl with manifestations of Kearns-Sayre and Lowe syndromes: an example of phenotypic mimicry?
    Moraes CT; Zeviani M; Schon EA; Hickman RO; Vlcek BW; DiMauro S
    Am J Med Genet; 1991 Dec; 41(3):301-5. PubMed ID: 1789283
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Deletions of mitochondrial DNA in Kearns-Sayre syndrome].
    Soga F; Ueno S; Yorifuji S
    Nihon Rinsho; 1993 Sep; 51(9):2386-90. PubMed ID: 8411717
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Transcription and translation of deleted mitochondrial genomes in Kearns-Sayre syndrome: implications for pathogenesis.
    Nakase H; Moraes CT; Rizzuto R; Lombes A; DiMauro S; Schon EA
    Am J Hum Genet; 1990 Mar; 46(3):418-27. PubMed ID: 1689952
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [A case of Kearns-Sayre syndrome whose asymptomatic mother had abnormal mitochondria in skeletal muscle].
    Akaike M; Kawai H; Kashiwagi S; Kunishige M; Saito S
    Rinsho Shinkeigaku; 1995 Feb; 35(2):190-4. PubMed ID: 7781238
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Oxidative damage to skeletal muscle DNA from patients with mitochondrial encephalomyopathies.
    Mitsui T; Kawai H; Nagasawa M; Kunishige M; Akaike M; Kimura Y; Saito S
    J Neurol Sci; 1996 Jul; 139(1):111-6. PubMed ID: 8836981
    [TBL] [Abstract][Full Text] [Related]  

  • 33. The clinical, myopathological, and genetic analysis of 155 Chinese mitochondrial ophthalmoplegia patients with mitochondrial DNA single large deletions.
    Zhao Y; Hou Y; Zhao X; Liufu T; Yu M; Zhang W; Xie Z; Zhang VW; Yuan Y; Wang Z
    Mol Genet Genomic Med; 2024 Jan; 12(1):e2328. PubMed ID: 38018320
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Chronic progressive external ophthalmoplegia (CPEO) with deleted mitochondrial DNA].
    Tanno Y; Yoneda M; Ohnishi Y; Miyatake T; Ozawa T
    Rinsho Shinkeigaku; 1989 Sep; 29(9):1176-9. PubMed ID: 2598547
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Expression of a defect in the respiratory chain in cultured human cells].
    Meola G; Rotondo G; Velicogna M; Toppi R; Sansone V; Bresolin N; Comi G; Bordoni A; Amati P; Ausenda C
    Riv Neurol; 1991; 61(4):122-34. PubMed ID: 1667713
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A novel 7.4 kb mitochondrial deletion in a patient with congenital progressive external ophthalmoplegia, muscle weakness and mental retardation.
    Tabaku M; Legius E; Robberecht W; Sciot R; Fryns JP; Cassiman JJ; Matthijs G
    Genet Couns; 1999; 10(3):285-93. PubMed ID: 10546101
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Deletion screening of mitochondrial DNA via multiprimer DNA amplification.
    Ernst BP; Wilichowski E; Wagner M; Hanefeld F
    Mol Cell Probes; 1994 Feb; 8(1):45-9. PubMed ID: 8028607
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Chronic progressive external ophthalmoplegia--symptom or syndrome?].
    Bau V; Deschauer M; Zierz S
    Klin Monbl Augenheilkd; 2009 Oct; 226(10):822-8. PubMed ID: 19830638
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia.
    Suomalainen A; Majander A; Haltia M; Somer H; Lönnqvist J; Savontaus ML; Peltonen L
    J Clin Invest; 1992 Jul; 90(1):61-6. PubMed ID: 1634620
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Mitochondrial respiratory chain diseases. Evaluation and variability in 52 patients].
    Arpa-Gutiérrez FJ; Cruz-Martínez A; Campos-González Y; Gutiérrez-Molina M; Santiago-Pérez S; Pérez-Conde MC; López-Pajares MR; Martín-Casarrubias MA; Rubio-Muñoz JC; del Hoyo P; Arpa-Fernández A; Arenas-Barbero J
    Rev Neurol; 2005 Oct 16-31; 41(8):449-54. PubMed ID: 16224730
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 34.