The molecular basis of new paediatric endocrine sindromes: POMC, LHX3 and NKX 2.1 deficiency sindromes Grüters, Krude, Biebermann, Netchine

Diagnostic and therapeutic aspects of GH deficiency (GHD) in the transition period Aimaretti, Baffoni, Corneli, Rovere, Gaia, Gasco, Ausiello, Grottoli, Ghigo

New trends in pediatric endocarditis Carceller, Lebel, Larose, Boutin