Alessandro Risio

Neurofibromatosis type I (NF1) and bone involvement in a pediatric setting: insights from FGF23 levels

Giulia Rodari, Valeria Citterio, Masami Ikehata, Deborah Mattinzoli et autres

BACKGROUND: Neurofibromatosis type I (NF1) is an autosomal dominant disorder characterized by extremely different phenotypes, sometimes including reduced bone mass. The underlying cause of bone impairment in these patients remains poorly understood, especially in children. Previous studies in mice and single reports …

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Neurofibromatosis Type I (NF1) and Bone Involvement in a pediatric setting: Insights from FGF23 Levels

Giulia Rodari, Valeria Citterio, Masami Ikehata, Deborah Mattinzoli et autres

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Bridging the gap between short stature and metabolic alterations in children born small for gestational age: an exploratory study

Rodari Pankiv Giulia, Valeria Citterio, Valentina Collini, Alessandro Risio et autres

Searchable abstracts of presentations at key conferences in endocrinology ISSN 1470-3947 (print) | ISSN 1479-6848 (online)