Coenzyme Q10

Botanical Source:Fermentation

Trademark:Q10 Pure

Specification:99.0% USP EP 

Efficacy:Cardiovascualr disease

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  • Basic Information
  • Pharmacological Effects
  • References
  • 7 Q10-1(3).jpg

  • 7 Q10-2(2).jpg

  • 1. Skladal D, Halliday J, Thorburn DR. Minimum birth prevalence of mitochondrial respiratory chain disorders in children. Brain 2003;126(Pt 8): 1905-12. 

    2. Mayr JA, Haack TB, Freisinger P, Karall D, Makowski C, Koch J, et al. Spectrum of combined respiratory chain defects. J Inherit Metab Dis 2015;38:629-40. 

    3. Saneto RP, Sedensky MM. Mitochondrial disease in childhood: mtDNA encoded. Neurotherapeutics 2013;10:199-211. 

    4. Poulton J, Finsterer J, Yu-Wai-Man P. Genetic counselling for maternally inherited mitochondrial disorders. Mol Diagn Ther 2017;21:419- 29. 

    5. Taylor RW, Pyle A, Griffin H, Blakely EL, Duff J, He L, et al. Use of whole-exome sequencing to determine the genetic basis of multiple mitochondrial respiratory chain complex deficiencies. JAMA 2014;312: 68-77. 

    6. von Dobeln U, Wibom R, Ahlman H, Nennesmo I, Nyctelius H, € Hultman E, et al. Fatal neonatal lactic acidosis with respiratory insufficiency due to complex I and IV deficiency. Acta Paediatr 1993;82: 1079-81. 7. Kishita Y, Paj