October 27, 2015

Methylation Mutations & Treatment: Intermediate Level Webinar

Dr. Stewart shares his clinical and biochemical experience to guide practitioners through the treatment of those with mutations that hinder the body's methyation process.

In this 30 minute webinar with Dr. Stewart we will discuss ten key topics often asked by practitioners:
  • What to do when you have a MTHFR genetic mutation
  • The 7 steps of the enzyme pathway that you have to pay attention to
  • What genetic SNPs should you pay attention to and what should you focus on first with treatment
  • How do you treat someone who does not have a MTHFR but is showing signs of a methylation deficiency
  • Why a FOLR 1, 2 and 3 mutation is just as important as a MTHFR
  • How do you treat someone who only has there MTHFR test results
  • When is the need for methylated vitamins more prominent in life
  • Treatment protocols with nutrition and symptoms a person may experience in the beginning
  • How to treat someone with symptoms but do not have genetic testing results
  • Gluathione SNPs that can help you guide a patient
For more lectures, webinars and articles by Dr. Stewart please email info@neurobiologix.com or visit www.DrNeurobiologix.com

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