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Giuseppa Patti

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European Journal of Endocrinology|May 5, 2021

The phenotypic spectrum associated with OTX2 mutations in humansLouise C Gregory, Peter Gergics, Marilena Nakaguma, et al.

Orphanet Journal of Rare Diseases|February 16, 2023

The Italian registry for patients with Prader-Willi syndromeMarco Salvatore, Paola Torreri, Graziano Grugni, et al.

Journal of Endocrinological Investigation|February 12, 2026

Understanding the burden of endocrine and metabolic disorders in Prader-Willi syndrome: data from the Italian registryGraziano Grugni, Adele Rocchetti, Carmen Bucolo, et al.

Journal of Endocrinological Investigation|April 28, 2026

Correction: Understanding the burden of endocrine and metabolic disorders in Prader-Willi syndrome: data from the Italian registryGraziano Grugni, Adele Rocchetti, Carmen Bucolo, et al.

Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society|September 6, 2019

Uniparental disomy and pretreatment IGF-1 may predict elevated IGF-1 levels in Prader-Willi patients on GH treatmentViviana Valeria Palmieri, Antonella Lonero, Sarah Bocchini, et al.

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Search research articles

Showing results (51-60 of 55) with videos related to

Sort By:

Pageof 6

You have reached the last page of results.This site can display upto 55 results.

European Journal of Endocrinology|May 5, 2021

The phenotypic spectrum associated with OTX2 mutations in humansLouise C Gregory, Peter Gergics, Marilena Nakaguma, et al.

Orphanet Journal of Rare Diseases|February 16, 2023

The Italian registry for patients with Prader-Willi syndromeMarco Salvatore, Paola Torreri, Graziano Grugni, et al.

Journal of Endocrinological Investigation|February 12, 2026

Understanding the burden of endocrine and metabolic disorders in Prader-Willi syndrome: data from the Italian registryGraziano Grugni, Adele Rocchetti, Carmen Bucolo, et al.

Journal of Endocrinological Investigation|April 28, 2026

Correction: Understanding the burden of endocrine and metabolic disorders in Prader-Willi syndrome: data from the Italian registryGraziano Grugni, Adele Rocchetti, Carmen Bucolo, et al.

Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society|September 6, 2019

Uniparental disomy and pretreatment IGF-1 may predict elevated IGF-1 levels in Prader-Willi patients on GH treatmentViviana Valeria Palmieri, Antonella Lonero, Sarah Bocchini, et al.

Pageof 6