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Spinocerebellar ataxia type 2 Spinocerebellar ataxia type 2a genetic neurodegenerative disorder due to a CAG repeat expansion mutation in the ATXN2 gene coding for the protein ataxin-2 63 has been associated to oxidative stress, in particular due to alterations in the enzymatic activity of antioxidant enzymes including GSTs 64
Sulfur is a sticky, smelly molecule that acts like flypaper trapping toxins in the body, explains Hyman
Cagrilintide (trials): once-weekly subcutaneous administration, escalated gradually over roughly six weeks to limit gastrointestinal effects
Rapid weight loss is often associated with muscle loss, nutritional deficiencies, and the likelihood of regaining weight
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