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Mutations in the POLG gene result in the forms of PEO specifically referred to as progressive external ophthalmoplegia with mitochondrial deletions, autosomal recessive 1 (PEOB1) and progressive external ophthalmoplegia with mitochondrial deletions, autosomal dominant 1 (PEOA1)

A randomized controlled clinical trial of topical insulin-like growth factor-1 therapy for sudden deafness refractory to systemic corticosteroid treatment

Stangel, M., Kuhlmann, T., Matthews, P

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Blending can damage the liposomes