S. Osimani

Guided Growth in Leg Length Discrepancy in Beckwith-Wiedemann Syndrome: A Consecutive Case Series

G. Barera, S. Russo, R. Pajno, 2021, Children.

Stimulated GH levels during the transition phase in Prader–Willi syndrome

A. Salvatoni, P. Marzullo, A. Sartorio, 2020, Journal of Endocrinological Investigation.

Molecular Mechanisms Generating and Stabilizing Terminal 22q13 Deletions in 44 Subjects with Phelan/McDermid Syndrome

M. Fichera, C. Romano, R. Borgatti, 2011, PLoS genetics.

A Long-term Competent Chimeric Immune System in a Dizygotic Dichorionic Twin

V. Biran, O. Baud, A. Verloes, 2011, Pediatrics.

Twin A Long-term Competent Chimeric Immune System in a Dizygotic Dichorionic

C. Baumann, A. Aboura, S. Drunat, 2011 .

Baraitser–Winter cerebrofrontofacial syndrome: delineation of the spectrum in 42 cases

B. V. van Bon, A. Hoischen, K. Devriendt, 2014, European Journal of Human Genetics.

The Hyperphagia Questionnaire: Insights From a Multicentric Validation Study in Individuals With Prader Willi Syndrome

A. Franzese, G. Valerio, D. Bacchini, 2022, Frontiers in Pediatrics.

The Italian registry for patients with Prader–Willi syndrome

M. Maghnie, D. Taruscio, M. Salvatore, 2023, Orphanet Journal of Rare Diseases.

Uniparental disomy and pretreatment IGF-1 may predict elevated IGF-1 levels in Prader-Willi patients on GH treatment.

A. Salvatoni, A. Franzese, F. Macchi, 2019, Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society.

Multicentric Italian case–control study on 25OH vitamin D levels in children and adolescents with Prader-Willi syndrome

M. Cappa, A. Crinò, G. Grugni, 2023, Journal of Endocrinological Investigation.