Paolo Emidio Macchia
University of Naples Federico II
78 papers found
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A Novel NKX2.1 Mutation in a Family with Hypothyroidism and Benign Hereditary Chorea
UploadA Mouse Model Demonstrates a Multigenic Origin of Congenital Hypothyroidism
Download from academic.oup.comHigh-dose intravenous corticosteroid therapy for Graves’ ophthalmopathy
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