Barth Syndrome – When the Lack of Fair, Equitable and Appropriate Regulatory Review Process Jeopardizes Ultra-Rare Drug Development Barth Syndrome Foundation Executive Director Emily Milligan, and Director of Family Services […]
Expert Series: At the crossroad of mitochondrial disease and mitochondrial dysfunction
Why are patients with Fibromyalgia, Chronic Fatigue, Lymes diagnosed with mitochondrial disease? How do I know I have Mito? What should my doctor look for to consider further testing for […]
Expert Series: Molecular Bypass Deoxynucleoside Therapy for Thymidine Kinase 2 Deficiency (TK2d)Expert Series:
Thymidine kinase 2 deficiency (TK2d) is a rare mitochondrial disease due to mutations in the TK2 gene (TK2). Deficiency of TK2 enzyme causes depletion and multiple deletions of mitochondrial DNA […]
Mitochondria and Psychiatry
This presentation will cover the evidence that, at least for a subset of people with bipolar disorder, mitochondria may be dysregulated in the brain. Medications used for bipolar disorder can […]
Meeting My MELAS Mito Friend
PARENTS AS RARE – EPISODE 070Meeting My MELAS Mito Friend – Elizabeth Wood I met Elizabeth Wood, a fellow mito patient, through connections at Mito Action. Elizabeth was the first […]
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