| Title | Author(s) | Year | View Count |
 | The cystic fibrosis transmembrane conductance regulator gene and ion channel function in patients with idiopathic pancreatitis | Bishop, MD; Freedman, SD; Zielenski, J; Ahmed, N; Dupuis, A; Martin, S; Ellis, L; Shea, J; Hopper, I; Corey, M; Kortan, P; Haber, G; Ross, C; Tzountzouris, J; Steele, L; Ray, PN; Tsui, LC; Durie, PR | 2005 | 834 |
| Increased prevalence of CFTR mutations and variants and decreased chloride secretion in primary sclerosing cholangitis | Sheth, S; Shea, JC; Bishop, MD; Chopra, S; Regan, MM; Malmberg, E; Walker, C; Ricci, R; Tsui, LC; Durie, PR; Zielenski, J; Freedman, SD | 2003 | 480 |
 | CFTR gene mutations and the pancreatic phenotype | Durie, PR; Ahmed, N; Corey, M; Zielenski, J; Ellis, L; Tullis, E; Tsui, LC | 1999 | 115 |
| Genotype/phenotype in relation to lung disease | Durie, PR; Tullis, E; Corey, M; Ellis, L; Martin, S; Jarvi, K; Zielenski, J; Gilljam, M; Tsui, LC | 1998 | 90 |
| Uncertainty in the diagnosis of cystic fibrosis: Possible role of in vivo nasal potential difference measurements | Wilson, DC; Ellis, L; Zielenski, J; Corey, M; Ip, WF; Tsui, LC; Tullis, E; Knowles, MR; Durie, PR | 1998 | 299 |
| Correlation of sweat chloride concentration with classes of the cystic fibrosis transmembrane conductance regulator gene mutations | Wilschanski, M; Zielenski, J; Markiewicz, D; Tsui, LC; Corey, M; Levison, H; Durie, PR | 1995 | 249 |
| The cystic fibrosis gene and resting energy expenditure | Fried, MD; Durie, PR; Tsui, LC; Corey, M; Levison, H; Pencharz, PB | 1991 | 242 |
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