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 *

112 related articles for article (PubMed ID: 8101271)

  • 1. Vitamin E in a mitochondrial myopathy with proliferating mitochondria.
    Bakker HD; Scholte HR; Jeneson JA
    Lancet; 1993 Jul; 342(8864):175-6. PubMed ID: 8101271
    [No Abstract]   [Full Text] [Related]  

  • 2. Adenine nucleotide translocator deficiency in muscle: potential therapeutic value of vitamin E.
    Bakker HD; Scholte HR; Van den Bogert C; Jeneson JA; Ruitenbeek W; Wanders RJ; Abeling NG; van Gennip AH
    J Inherit Metab Dis; 1993; 16(3):548-52. PubMed ID: 7609449
    [No Abstract]   [Full Text] [Related]  

  • 3. 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]  

  • 4. Mitochondrial myopathies: diagnosis, exercise intolerance, and treatment options.
    Tarnopolsky MA; Raha S
    Med Sci Sports Exerc; 2005 Dec; 37(12):2086-93. PubMed ID: 16331134
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mitochondrial creatine kinase activity in patients with disturbed energy generation in muscle mitochondria.
    Smeitink J; Ruitenbeek W; Sengers R; Wevers R; van Lith T; Trijbels F
    J Inherit Metab Dis; 1994; 17(1):67-73. PubMed ID: 8051938
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mitochondrial defects and anesthetic sensitivity.
    Morgan PG; Hoppel CL; Sedensky MM
    Anesthesiology; 2002 May; 96(5):1268-70. PubMed ID: 11981173
    [No Abstract]   [Full Text] [Related]  

  • 7. Very low levels of the mtDNA A3243G mutation associated with mitochondrial dysfunction in vivo.
    Chinnery PF; Taylor DJ; Brown DT; Manners D; Styles P; Lodi R
    Ann Neurol; 2000 Mar; 47(3):381-4. PubMed ID: 10716261
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The end of the road.
    Derr M
    Sci Am; 1995 Apr; 272(4):16, 20. PubMed ID: 7716484
    [No Abstract]   [Full Text] [Related]  

  • 9. Low levels of mitochondrial transcription factor A in mitochondrial DNA depletion.
    Larsson NG; Oldfors A; Holme E; Clayton DA
    Biochem Biophys Res Commun; 1994 May; 200(3):1374-81. PubMed ID: 8185589
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Mitochondrial myopathies. Diagnostic approaches and genetic counseling].
    Monastiri K; Snoussi N
    Tunis Med; 1995 Feb; 73(2):87-94. PubMed ID: 9506149
    [No Abstract]   [Full Text] [Related]  

  • 11. Mitochondrial myopathies.
    DiMauro S
    Curr Opin Rheumatol; 2006 Nov; 18(6):636-41. PubMed ID: 17053512
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Lipid myopathy associated with renal tubular acidosis and spastic diplegia in two brothers.
    Tung YC; Tsau YK; Chu LW; Young C; Shen YZ
    J Formos Med Assoc; 2001 Jul; 100(7):484-7. PubMed ID: 11579615
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Mitochondrial myopathy in rheumatology: comment on the article by Albert et al.
    Carey JJ; Coughlan RJ; O'Sullivan M
    Arthritis Care Res (Hoboken); 2012 Jul; 64(7):1099; author reply 1099-100. PubMed ID: 22238193
    [No Abstract]   [Full Text] [Related]  

  • 15. Control of oxidative phosphorylation in muscle.
    Radda GK; Kemp GJ; Styles P; Taylor DJ
    Biochem Soc Trans; 1993 Aug; 21 ( Pt 3)(3):762-4. PubMed ID: 8224506
    [No Abstract]   [Full Text] [Related]  

  • 16. Mitochondrial DNA depletion in single fibers in a patient with novel TK2 mutations.
    Roos S; Lindgren U; Ehrstedt C; Moslemi AR; Oldfors A
    Neuromuscul Disord; 2014 Aug; 24(8):713-20. PubMed ID: 24953930
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Mitochondrial and metabolic myopathies].
    de Wazières B; Dupond JL
    Rev Prat; 2001 Feb; 51(3):256-61. PubMed ID: 11265421
    [TBL] [Abstract][Full Text] [Related]  

  • 18. ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency.
    Olsen RK; Olpin SE; Andresen BS; Miedzybrodzka ZH; Pourfarzam M; Merinero B; Frerman FE; Beresford MW; Dean JC; Cornelius N; Andersen O; Oldfors A; Holme E; Gregersen N; Turnbull DM; Morris AA
    Brain; 2007 Aug; 130(Pt 8):2045-54. PubMed ID: 17584774
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Metabolic diseases of skeletal muscle: clues to understanding exercise physiology.
    Scheen AJ
    Eur J Med; 1992 Dec; 1(8):453-6. PubMed ID: 1341203
    [No Abstract]   [Full Text] [Related]  

  • 20. Disturbance of mitochondrial functions provoked by the major long-chain 3-hydroxylated fatty acids accumulating in MTP and LCHAD deficiencies in skeletal muscle.
    Cecatto C; Godoy KDS; da Silva JC; Amaral AU; Wajner M
    Toxicol In Vitro; 2016 Oct; 36():1-9. PubMed ID: 27371118
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.