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Alessandro Salvatoni

Showing results (31-40 of 38) with videos related to

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BMC Medical Genetics|March 17, 2009
Prevalence of pathogenetic MC4R mutations in Italian children with early onset obesity, tall stature and familial history of obesityNicola Santoro, Grazia Cirillo, Zhimin Xiang, et al.
Clinical Endocrinology|December 14, 2011
Assessment of central adrenal insufficiency in children and adolescents with Prader-Willi syndromeAndrea Corrias, Graziano Grugni, Antonino Crinò, et al.
Pediatric Diabetes|March 19, 2016
The role of socio-economic and clinical factors on HbA1c in children and adolescents with type 1 diabetes: an Italian multicentre surveyRosaria Gesuita, Edlira Skrami, Riccardo Bonfanti, et al.
American Journal of Medical Genetics. Part A|July 31, 2019
Anthropometric characteristics of newborns with Prader-Willi syndromeAlessandro Salvatoni, Alex Moretti, Graziano Grugni, 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.
Frontiers in Endocrinology|May 13, 2024
Endocrine features of Prader-Willi syndrome: a narrative review focusing on genotype-phenotype correlationSimona F Madeo, Luca Zagaroli, Sara Vandelli, et al.
American Journal of Medical Genetics. Part A|January 19, 2008
The Italian National Survey for Prader-Willi syndrome: an epidemiologic studyGraziano Grugni, Antonino Crinò, Laura Bosio, et al.
Acta Diabetologica|May 18, 2026
Screening practices for diabetic peripheral neuropathy in pediatric type 1 diabetes: a nationwide survey by the ISPED Diabetes Study GroupBruno Bombaci, Marta Bassi, Valeria Castorani, et al.
Pageof 4

Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
BMC Medical Genetics|March 17, 2009
Prevalence of pathogenetic MC4R mutations in Italian children with early onset obesity, tall stature and familial history of obesityNicola Santoro, Grazia Cirillo, Zhimin Xiang, et al.
Clinical Endocrinology|December 14, 2011
Assessment of central adrenal insufficiency in children and adolescents with Prader-Willi syndromeAndrea Corrias, Graziano Grugni, Antonino Crinò, et al.
Pediatric Diabetes|March 19, 2016
The role of socio-economic and clinical factors on HbA1c in children and adolescents with type 1 diabetes: an Italian multicentre surveyRosaria Gesuita, Edlira Skrami, Riccardo Bonfanti, et al.
American Journal of Medical Genetics. Part A|July 31, 2019
Anthropometric characteristics of newborns with Prader-Willi syndromeAlessandro Salvatoni, Alex Moretti, Graziano Grugni, 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.
Frontiers in Endocrinology|May 13, 2024
Endocrine features of Prader-Willi syndrome: a narrative review focusing on genotype-phenotype correlationSimona F Madeo, Luca Zagaroli, Sara Vandelli, et al.
American Journal of Medical Genetics. Part A|January 19, 2008
The Italian National Survey for Prader-Willi syndrome: an epidemiologic studyGraziano Grugni, Antonino Crinò, Laura Bosio, et al.
Acta Diabetologica|May 18, 2026
Screening practices for diabetic peripheral neuropathy in pediatric type 1 diabetes: a nationwide survey by the ISPED Diabetes Study GroupBruno Bombaci, Marta Bassi, Valeria Castorani, et al.
Pageof 4