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Last Published 11.01.2025 Effective Date: 11.01.2025 This policy addresses alpha1-proteinase inhibitors (Aralast NP, Glassia, Prolastin-C, and Zemaira) for chronic augmentation and maintenance therapy of emphysema due to congenital deficiency of alpha1-proteinase inhibitor (A1-PI)/alpha1-antitrypsin (AAT) deficiency

For example, a decrease in motor activity could reflect less motivation to initiate locomotion, but could also be associated with a deficit in motor function

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