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Minerva Pediatrica|September 16, 2009
Identification and management of dyslipidemic childrenO Guardamagna, V Baracco, F Abello, et al.Pediatrie|January 1, 1987
[Trial of indirect screening of tetrahydrobiopterin deficiency]S Ferraris, O Guardamagna, G Bracco, et al.Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|February 16, 2010
The treatment of hypercholesterolemic children: efficacy and safety of a combination of red yeast rice extract and policosanolsO Guardamagna, F Abello, V Baracco, et al.Journal of Inherited Metabolic Disease|January 1, 1986
Tetrahydrobiopterin non-responsiveness in dihydropteridine reductase deficiency is associated with the presence of mutant proteinR G Cotton, I Jennings, G Bracco, et al.Archives of Disease in Childhood|February 1, 1988
Two mutations of dihydropteridine reductase deficiencyA Ponzone, O Guardamagna, S Ferraris, et al.European Journal of Pediatrics|August 1, 1993
Differential diagnosis of hyperphenylalaninaemia by a combined phenylalanine-tetrahydrobiopterin loading testA Ponzone, O Guardamagna, M Spada, et al.Minerva Pediatrica|June 19, 2002
[Influence of diet on lipoprotein profile in familial combined hyperlipidemia affected children]C Bondone, E Rutto, M Giaccone, et al.Pediatric Research|November 1, 1991
Tetrahydrobiopterin loading test in hyperphenylalaninemiaA Ponzone, O Guardamagna, S Ferraris, et al.European Journal of Pediatrics|August 1, 1986
Prenatal diagnosis of "dihydrobiopterin synthetase" deficiency, a variant form of phenylketonuriaA Niederwieser, H Shintaku, T Hasler, et al.Neuropharmacology|October 31, 2001
Prolonged exposure to YC-1 induces apoptosis in adrenomedullary endothelial and chromaffin cells through a cGMP-independent mechanismR Ferrero, M TorresPageof 9