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 *

104 related articles for article (PubMed ID: 14569122)

  • 1. A tRNA(Ala) mutation causing mitochondrial myopathy clinically resembling myotonic dystrophy.
    Horváth R; Lochmüller H; Scharfe C; Do BH; Oefner PJ; Müller-Höcker J; Schoser BG; Pongratz D; Auer DP; Jaksch M
    J Med Genet; 2003 Oct; 40(10):752-7. PubMed ID: 14569122
    [No Abstract]   [Full Text] [Related]  

  • 2. Pure myopathy associated with a novel mitochondrial tRNA gene mutation.
    Swalwell H; Deschauer M; Hartl H; Strauss M; Turnbull DM; Zierz S; Taylor RW
    Neurology; 2006 Feb; 66(3):447-9. PubMed ID: 16476954
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The m.5650G>A mitochondrial tRNAAla mutation is pathogenic and causes a phenotype of pure myopathy.
    McFarland R; Swalwell H; Blakely EL; He L; Groen EJ; Turnbull DM; Bushby KM; Taylor RW
    Neuromuscul Disord; 2008 Jan; 18(1):63-7. PubMed ID: 17825557
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A mitochondrial tRNA aspartate mutation causing isolated mitochondrial myopathy.
    Seneca S; Goemans N; Van Coster R; Givron P; Reybrouck T; Sciot R; Meulemans A; Smet J; Van Hove JL
    Am J Med Genet A; 2005 Aug; 137(2):170-5. PubMed ID: 16059939
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mitochondrial myopathy mimicking fibromyalgia syndrome.
    Villanova M; Selvi E; Malandrini A; Casali C; Santorelli FM; De Stefano R; Marcolongo R
    Muscle Nerve; 1999 Feb; 22(2):289-91. PubMed ID: 10024147
    [No Abstract]   [Full Text] [Related]  

  • 6. Late-onset mitochondrial myopathy with dystrophic changes due to a G7497A mutation in the mitochondrial tRNA(Ser(UCN)) gene.
    Müller T; Deschauer M; Neudecker S; Zierz S
    Acta Neuropathol; 2005 Oct; 110(4):426-30. PubMed ID: 16133542
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cardiac involvement in patients with myotonic dystrophy, Becker's muscular dystrophy and mitochondrial myopathy.
    Finsterer J; Stöllberger C; Keller H; Slany J; Mamoli B
    Herz; 1997 Apr; 22(2):96-103. PubMed ID: 9134443
    [TBL] [Abstract][Full Text] [Related]  

  • 8. When should a rheumatologist suspect a mitochondrial myopathy?
    Albert DA; Cohen JA; Burns CM; Hickey WF; Prock TL; James JA; Rhodes CH; Wortmann RL
    Arthritis Care Res (Hoboken); 2011 Nov; 63(11):1497-502. PubMed ID: 22034111
    [No Abstract]   [Full Text] [Related]  

  • 9. Mitochondrial myopathy in a child with a muscle-restricted mutation in the mitochondrial transfer RNAAsn gene.
    Bruno C; Cassandrini D; Fattori F; Pedemonte M; Fiorillo C; Brigati G; Brisca G; Minetti C; Santorelli FM
    Biochem Biophys Res Commun; 2011 Sep; 412(4):518-21. PubMed ID: 21741368
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Human cultured myoblasts: a model for the diagnosis of mitochondrial diseases.
    Dumoulin R; Mandon G; Collombet JM; Blond JL; Carrier H; Godinot C; Flocard F; Villard J; Guibaud P; Mathieu M
    J Inherit Metab Dis; 1993; 16(3):545-7. PubMed ID: 7609448
    [No Abstract]   [Full Text] [Related]  

  • 11. [Heart muscle involvement in myopathies].
    Finsterer J; Stoellberger C; Keller H; Slany J; Mamoli B
    Wien Med Wochenschr; 1996; 146(9-10):212. PubMed ID: 9012218
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mitochondrial myopathy with autophagic vacuoles in patients with the m.8344A>G mutation.
    Yuan JH; Sakiyama Y; Higuchi I; Inamori Y; Higuchi Y; Hashiguchi A; Higashi K; Yoshimura A; Takashima H
    J Clin Pathol; 2013 Aug; 66(8):659-64. PubMed ID: 23559353
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Muscle structural changes in mitochondrial myopathy relate to genotype.
    Olsen DB; Langkilde AR; Ørngreen MC; Rostrup E; Schwartz M; Vissing J
    J Neurol; 2003 Nov; 250(11):1328-34. PubMed ID: 14648149
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Detection of mitochondrial defects by laser fluorimetry.
    Kunz WS; Winkler K; Kuznetsov AV; Lins H; Kirches E; Wallesch CW
    Mol Cell Biochem; 1997 Sep; 174(1-2):97-100. PubMed ID: 9309672
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Morphological changes of mitochondrial myopathies].
    Cabello A; Navarro C; Ricoy JR
    Rev Neurol; 1998 Apr; 26 Suppl 1():S44-9. PubMed ID: 9810590
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Limited diagnostic value of enzyme analysis in patients with mitochondrial tRNA mutations.
    Wibrand F; Jeppesen TD; Frederiksen AL; Olsen DB; Duno M; Schwartz M; Vissing J
    Muscle Nerve; 2010 May; 41(5):607-13. PubMed ID: 19941338
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mitochondrial myopathies.
    Larsson NG; Oldfors A
    Acta Physiol Scand; 2001 Mar; 171(3):385-93. PubMed ID: 11412152
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A mitochondrial DNA duplication as a marker of skeletal muscle specific mutations in the mitochondrial genome.
    Mancuso M; Vives-Bauza C; Filosto M; Marti R; Solano A; Montoya J; Gamez J; DiMauro S; Andreu AL
    J Med Genet; 2004 Jun; 41(6):e73. PubMed ID: 15173239
    [No Abstract]   [Full Text] [Related]  

  • 19. [Mitochondrial DNA mutation analysis in patients with mitochondrial myopathy].
    Zhang XA; Wu HC; Zhang BF; Yu W; Fan QS
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Feb; 22(1):18-21. PubMed ID: 15696472
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Altered skeletal muscle (mitochondrial) properties in patients with mitochondrial DNA single deletion myopathy.
    Gehrig SM; Mihaylova V; Frese S; Mueller SM; Ligon-Auer M; Spengler CM; Petersen JA; Lundby C; Jung HH
    Orphanet J Rare Dis; 2016 Jul; 11(1):105. PubMed ID: 27473873
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.