BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

122 related articles for article (PubMed ID: 26103814)

  • 1. [Effect of sodium pyruvate on exercise intolerance and muscle weakness due to mitochondrial myopathy: a case report].
    Kuroha Y; Tada M; Kawachi I; Nishizawa M; Matsubara N; Koike R
    Rinsho Shinkeigaku; 2015; 55(6):412-6. PubMed ID: 26103814
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Isolated mitochondrial myopathy associated with muscle coenzyme Q10 deficiency.
    Lalani SR; Vladutiu GD; Plunkett K; Lotze TE; Adesina AM; Scaglia F
    Arch Neurol; 2005 Feb; 62(2):317-20. PubMed ID: 15710863
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Exercise intolerance in mitochondrial myopathy is not related to lactic acidosis.
    Vissing J; Gansted U; Quistorff B
    Ann Neurol; 2001 May; 49(5):672-6. PubMed ID: 11357960
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Exercise intolerance in patients with McArdle's disease or mitochondrial myopathies.
    Chaussain M; Camus F; Defoligny C; Eymard B; Fardeau M
    Eur J Med; 1992 Dec; 1(8):457-63. PubMed ID: 1341204
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mitochondrial myopathy with exercise intolerance and retinal dystrophy in a sporadic patient with a G583A mutation in the mt tRNA(phe) gene.
    Darin N; Kollberg G; Moslemi AR; Tulinius M; Holme E; Grönlund MA; Andersson S; Oldfors A
    Neuromuscul Disord; 2006 Aug; 16(8):504-6. PubMed ID: 16806928
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Muscle fatigue, lactate, and pyruvate in mitochondrial myopathy with progressive external ophthalmoplegia.
    Dengler R; Wohlfarth K; Zierz S; Jobges M; Schubert M
    Muscle Nerve; 1996 Apr; 19(4):456-62. PubMed ID: 8622724
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Episodic weakness associated with exertional lactic acidosis and myopathy in Old English sheepdog littermates.
    Breitschwerdt EB; Kornegay JN; Wheeler SJ; Stevens JB; Baty CJ
    J Am Vet Med Assoc; 1992 Sep; 201(5):731-6. PubMed ID: 1399775
    [TBL] [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. Pure exercise intolerance and ophthalmoplegia associated with the m.12,294G > A mutation in the MT-TL2 gene: a case report.
    Soldath P; Madsen KL; Buch AE; Duno M; Wibrand F; Vissing J
    BMC Musculoskelet Disord; 2017 Oct; 18(1):419. PubMed ID: 29052516
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA.
    Andreu AL; Hanna MG; Reichmann H; Bruno C; Penn AS; Tanji K; Pallotti F; Iwata S; Bonilla E; Lach B; Morgan-Hughes J; DiMauro S
    N Engl J Med; 1999 Sep; 341(14):1037-44. PubMed ID: 10502593
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Noninflammatory myopathies.
    Baer AN; Wortmann RL
    Rheum Dis Clin North Am; 2013 May; 39(2):457-79. PubMed ID: 23597974
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Mitochondrial myopathy with autosomal dominant inheritance--report of a family and review of the literature].
    Kawai H; Akaike M; Yokoi K; Tamaki Y; Saito S
    Rinsho Shinkeigaku; 1993 Feb; 33(2):162-8. PubMed ID: 8319387
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Exercise training in mitochondrial myopathy: a randomized controlled trial.
    Cejudo P; Bautista J; Montemayor T; Villagómez R; Jiménez L; Ortega F; Campos Y; Sánchez H; Arenas J
    Muscle Nerve; 2005 Sep; 32(3):342-50. PubMed ID: 15962332
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A mitochondrial tRNA(Met) mutation causing developmental delay, exercise intolerance and limb girdle phenotype with onset in early childhood.
    Born AP; Duno M; Rafiq J; Risom L; Wibrand F; Østergaard E; Vissing J
    Eur J Paediatr Neurol; 2015 Jan; 19(1):69-71. PubMed ID: 25468263
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Combination of mitochondrial myopathy and biventricular hypertrabeculation/noncompaction.
    Wang J; Kong X; Han P; Hu B; Cao F; Liu Y; Zhu Q
    Neuromuscul Disord; 2016 Feb; 26(2):165-9. PubMed ID: 26707596
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mitochondrial myopathy presenting as rhabdomyolysis.
    Patchett DC; Grover ML
    J Am Osteopath Assoc; 2011 Jun; 111(6):404-5. PubMed ID: 21771927
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Hypothyroid myopathy: a case report].
    Tsai WP; Liou LB; Chu CC; Huang CC; Chiou SC; Luo SF
    J Microbiol Immunol Infect; 1999 Jun; 32(2):133-6. PubMed ID: 11565566
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical Features, Molecular Heterogeneity, and Prognostic Implications in YARS2-Related Mitochondrial Myopathy.
    Sommerville EW; Ng YS; Alston CL; Dallabona C; Gilberti M; He L; Knowles C; Chin SL; Schaefer AM; Falkous G; Murdoch D; Longman C; de Visser M; Bindoff LA; Rawles JM; Dean JCS; Petty RK; Farrugia ME; Haack TB; Prokisch H; McFarland R; Turnbull DM; Donnini C; Taylor RW; Gorman GS
    JAMA Neurol; 2017 Jun; 74(6):686-694. PubMed ID: 28395030
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel sporadic mutation G14739A of the mitochondrial tRNA(Glu) in a girl with exercise intolerance.
    Mayr JA; Moslemi AR; Förster H; Kamper A; Idriceanu C; Muss W; Huemer M; Oldfors A; Sperl W
    Neuromuscul Disord; 2006 Dec; 16(12):874-7. PubMed ID: 17056256
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.