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Definition and diagnostic criteria Hereditary glutathione synthetase deficiency is a rare autosomal recessive disease characterized by hemolytic anemia, metabolic acidosis, 5-oxoprolinuria, progressive neurological symptoms and recurrent bacterial infections

Effect of vanillic acid on COQ6 mutants identified in patients with coenzyme Q10 deficiency

Reasons patients give for stopping include reaching a plateau in weight loss, inability to tolerate side effects, or even inability to get the medication due to shortages

By the end of the year, she had gained 20 pounds

Chronic HPA activation elevates cortisol production, lowering immune responses and the production of proinflammatory cytokines

Brain and body disconnect: A retrospective case series of subacute combined degeneration of the spinal cord from chronic nitrous oxide use