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doi: 10.1016/S0140-6736(02)07340-3 Summary Keywords Prader-Willi syndrome (PWS), genotype-phenotype correlation, growth hormone (GH), metabolic syndrome, hypogonadism, bone metabolism, type 2 diabetes, thyroid Citation Madeo SF, Zagaroli L, Vandelli S, Calcaterra V, Crin A, De Sanctis L, Faienza MF, Fintini D, Guazzarotti L, Licenziati MR, Mozzillo E, Pajno R, Scarano E, Street ME, Wasniewska M, Bocchini S, Bucolo C, Buganza R, Chiarito M, Corica D, Di Candia F, Francavilla R, Fratangeli N, Improda N, Morabito LA, Mozzato C, Rossi V, Schiavariello C, Farello G, Iughetti L, Salpietro V, Salvatoni A, Giordano M, Grugni G and Delvecchio M (2024) Endocrine features of Prader-Willi syndrome: a narrative review focusing on genotype-phenotype correlation

BPC-157s ability to produce context-dependent nitric oxide regulation distinguishes it from simple vasodilators

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