Isabelle Gennero

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Editor Albright hereditary osteodystrophy (AHO) is a rare autosomal dominant disease caused by inactivating mutations in the GNAS gene, located on the chromosome 20. GNAS gene encodes Gsa, the a(More)
BACKGROUND Children with Prader-Willi syndrome (PWS) are routinely treated with GH and have a response comparable with that observed in children with GH deficiency (GHD). OBJECTIVE The objective of(More)