CFTR mutations and IVS8-5T variant in newborns with hypertrypsinaemia and normal sweat test.

Por Castellani, C, Bonizzato, A, Mastella, G
Publicado em 1997

Protracted neonatal hypertrypsinogenaemia, normal sweat chloride, and cystic fibrosis

Por Castellani, C, Tamanini, A, Mastella, G
Publicado em 2000

Burkholderia cepacia and delta F508 homozygosity in cystic fibrosis.

Por Castellani, C, Bonizzato, A, Cazzola, G A, Amalfitano, G, Mastella, G
Publicado em 1995

Cystic fibrosis mutations in heterozygous newborns with hypertrypsinemia and low sweat chloride.

Por Castellani, C, Benetazzo, M G, Bonizzato, A, Pignatti, P F, Mastella, G
Publicado em 1999

Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in neonatal hypertrypsinaemia with normal sweat test

Por CASTELLANI, C., BENETAZZO, M. G., TAMANINI, A., BEGNINI, A., MASTELLA, G., PIGNATTI, P.
Publicado em 2001

Cystic fibrosis: terminology and diagnostic algorithms

Por De Boeck, K, Wilschanski, M, Castellani, C, Taylor, C, Cuppens, H, Dodge, J, Sinaasappel, M
Publicado em 2006

High frequency of cystic fibrosis transmembrane regulator mutation L997F in patients with recurrent idiopathic pancreatitis and in newborns with hypertrypsinemia.

Por Gomez Lira M, Benetazzo, M G, Marzari, M G, Bombieri, C, Belpinati, F, Castellani, C, Cavallini, G C, Mastella, G, Pignatti, P F
Publicado em 2000

Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practice

Por Castellani, C., Cuppens, H., Macek, M., Cassiman, J.J., Kerem, E., Durie, P., Tullis, E., Assael, B.M., Bombieri, C., Brown, A., Casals, T., Claustres, M., Cutting, G.R., Dequeker, E., Dodge, J., Doull, I., Farrell, P., Ferec, C., Girodon, E., Johannesson, M., Kerem, B., Knowles, M., Munck, A., Pignatti, P.F., Radojkovic, D., Rizzotti, P., Schwarz, M., Stuhrmann, M., Tzetis, M., Zielenski, J., Elborn, J.S.
Publicado em 2008