Prolonged exclusive breast feeding and hereditary as determinants in infantile atopy.

Por Ponzone, A
Publicado em 1987

Two mutations of dihydropteridine reductase deficiency.

Por Ponzone, A, Guardamagna, O, Ferraris, S, Bracco, G, Niederwieser, A, Cotton, R G
Publicado em 1988

Screening for mutations in the phenylalanine hydroxylase gene from Italian patients with phenylketonuria by using the chemical cleavage method: a new splice mutation.

Por Dianzani, I, Forrest, S M, Camaschella, C, Saglio, G, Ponzone, A, Cotton, R G
Publicado em 1991

Genetic history of phenylketonuria mutations in Italy.

Por Dianzani, I., Giannattasio, S., de Sanctis, L., Marra, E., Ponzone, A., Camaschella, C., Piazza, A.
Publicado em 1994

Molecular analysis of contiguous exons of the phenylalanine hydroxylase gene: identification of a new PKU mutation.

Por Dianzani, I, Camaschella, C, Saglio, G, Ferrero, G B, Ramus, S, Ponzone, A, Cotton, R G
Publicado em 1993

Two new mutations in the dihydropteridine reductase gene in patients with tetrahydrobiopterin deficiency.

Por Dianzani, I, Howells, D W, Ponzone, A, Saleeba, J A, Smooker, P M, Cotton, R G
Publicado em 1993

Localization, by linkage analysis, of the cystinuria type III gene to chromosome 19q13.1.

Por Bisceglia, L, Calonge, M J, Totaro, A, Feliubadaló, L, Melchionda, S, García, J, Testar, X, Gallucci, M, Ponzone, A, Zelante, L, Zorzano, A, Estivill, X, Gasparini, P, Nunes, V, Palacín, M
Publicado em 1997

A European multicenter study of phenylalanine hydroxylase deficiency: classification of 105 mutations and a general system for genotype-based prediction of metabolic phenotype.

Por Guldberg, P, Rey, F, Zschocke, J, Romano, V, François, B, Michiels, L, Ullrich, K, Hoffmann, G F, Burgard, P, Schmidt, H, Meli, C, Riva, E, Dianzani, I, Ponzone, A, Rey, J, Güttler, F
Publicado em 1998