Zielenski J - Search Results

1

Role of cystic fibrosis transmembrane conductance regulator in patients with chronic sinopulmonary disease.

Gonska T, Choi P, Stephenson A, Ellis L, Martin S, Solomon M, Dupuis A, Dorfman R, Zielenski J, Ooi CY, Weiser W, Durie PR, Tullis E. Gonska T, et al. Among authors: zielenski j. Chest. 2012 Oct;142(4):996-1004. doi: 10.1378/chest.11-2543. Chest. 2012. PMID: 22423042

2

Clinical manifestations of cystic fibrosis among patients with diagnosis in adulthood.

Gilljam M, Ellis L, Corey M, Zielenski J, Durie P, Tullis DE. Gilljam M, et al. Among authors: zielenski j. Chest. 2004 Oct;126(4):1215-24. doi: 10.1378/chest.126.4.1215. Chest. 2004. PMID: 15486385

3

Mutations in the cystic fibrosis transmembrane regulator gene and in vivo transepithelial potentials.

Wilschanski M, Dupuis A, Ellis L, Jarvi K, Zielenski J, Tullis E, Martin S, Corey M, Tsui LC, Durie P. Wilschanski M, et al. Among authors: zielenski j. Am J Respir Crit Care Med. 2006 Oct 1;174(7):787-94. doi: 10.1164/rccm.200509-1377OC. Epub 2006 Jul 13. Am J Respir Crit Care Med. 2006. PMID: 16840743 Free PMC article.

4

Type of CFTR mutation determines risk of pancreatitis in patients with cystic fibrosis.

Ooi CY, Dorfman R, Cipolli M, Gonska T, Castellani C, Keenan K, Freedman SD, Zielenski J, Berthiaume Y, Corey M, Schibli S, Tullis E, Durie PR. Ooi CY, et al. Among authors: zielenski j. Gastroenterology. 2011 Jan;140(1):153-61. doi: 10.1053/j.gastro.2010.09.046. Epub 2010 Nov 9. Gastroenterology. 2011. PMID: 20923678

5

Does extensive genotyping and nasal potential difference testing clarify the diagnosis of cystic fibrosis among patients with single-organ manifestations of cystic fibrosis?

Ooi CY, Dupuis A, Ellis L, Jarvi K, Martin S, Ray PN, Steele L, Kortan P, Gonska T, Dorfman R, Solomon M, Zielenski J, Corey M, Tullis E, Durie P. Ooi CY, et al. Among authors: zielenski j. Thorax. 2014 Mar;69(3):254-60. doi: 10.1136/thoraxjnl-2013-203832. Epub 2013 Oct 21. Thorax. 2014. PMID: 24149827

6

Does integration of various ion channel measurements improve diagnostic performance in cystic fibrosis?

Ooi CY, Dupuis A, Gonska T, Ellis L, Ni A, Jarvi K, Martin S, Ray P, Steele L, Kortan P, Dorfman R, Solomon M, Zielenski J, Corey M, Tullis E, Durie P. Ooi CY, et al. Among authors: zielenski j. Ann Am Thorac Soc. 2014 May;11(4):562-70. doi: 10.1513/AnnalsATS.201311-412OC. Ann Am Thorac Soc. 2014. PMID: 24697796

7

Molecular consequences of cystic fibrosis transmembrane regulator (CFTR) gene mutations in the exocrine pancreas.

Ahmed N, Corey M, Forstner G, Zielenski J, Tsui LC, Ellis L, Tullis E, Durie P. Ahmed N, et al. Among authors: zielenski j. Gut. 2003 Aug;52(8):1159-64. doi: 10.1136/gut.52.8.1159. Gut. 2003. PMID: 12865275 Free PMC article.

8

The prevalence and clinical characteristics of cystic fibrosis in South Asian Canadian immigrants.

Mei-Zahav M, Durie P, Zielenski J, Solomon M, Tullis E, Tsui LC, Corey M. Mei-Zahav M, et al. Among authors: zielenski j. Arch Dis Child. 2005 Jul;90(7):675-9. doi: 10.1136/adc.2003.042614. Arch Dis Child. 2005. PMID: 15970608 Free PMC article.

9

Genotype and phenotype correlations in patients with cystic fibrosis and pancreatitis.

Durno C, Corey M, Zielenski J, Tullis E, Tsui LC, Durie P. Durno C, et al. Among authors: zielenski j. Gastroenterology. 2002 Dec;123(6):1857-64. doi: 10.1053/gast.2002.37042. Gastroenterology. 2002. PMID: 12454843

10

Glucose intolerance in children with cystic fibrosis.

Solomon MP, Wilson DC, Corey M, Kalnins D, Zielenski J, Tsui LC, Pencharz P, Durie P, Sweezey NB. Solomon MP, et al. Among authors: zielenski j. J Pediatr. 2003 Feb;142(2):128-32. doi: 10.1067/mpd.2003.5. J Pediatr. 2003. PMID: 12584532

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