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Hyperphenylalaninemia and pterin metabolism in serum and erythrocytes.
Ponzone A, Guardamagna O, Spada M, Ponzone R, Sartore M, Kierat L, Heizmann CW, Blau N. Ponzone A, et al. Among authors: guardamagna o. Clin Chim Acta. 1993 Jul 16;216(1-2):63-71. doi: 10.1016/0009-8981(93)90139-u. Clin Chim Acta. 1993. PMID: 8222274
Prenatal diagnosis of atypical phenylketonuria.
Blau N, Niederwieser A, Curtius HC, Kierat L, Leimbacher W, Matasovic A, Binkert F, Lehmann H, Leupold D, Guardamagna O, et al. Blau N, et al. Among authors: guardamagna o. J Inherit Metab Dis. 1989;12 Suppl 2:295-8. doi: 10.1007/BF03335403. J Inherit Metab Dis. 1989. PMID: 2480478 No abstract available.
Tetrahydrobiopterin loading test in hyperphenylalaninemia.
Ponzone A, Guardamagna O, Ferraris S, Ferrero GB, Dianzani I, Cotton RG. Ponzone A, et al. Among authors: guardamagna o. Pediatr Res. 1991 Nov;30(5):435-8. doi: 10.1203/00006450-199111000-00008. Pediatr Res. 1991. PMID: 1754298
Two mutations of dihydropteridine reductase deficiency.
Ponzone A, Guardamagna O, Ferraris S, Bracco G, Niederwieser A, Cotton RG. Ponzone A, et al. Among authors: guardamagna o. Arch Dis Child. 1988 Feb;63(2):154-7. doi: 10.1136/adc.63.2.154. Arch Dis Child. 1988. PMID: 2894818 Free PMC article.
82 results