Similar articles for PMID: 15286159

Year	Number of Results
1966	1
1967	1
1970	3
1971	1
1972	2
1973	2
1978	1
1979	1
1980	2
1981	1
1982	1
1983	1
1985	1
1986	2
1987	1
1988	1
1992	1
1993	1
1995	3
1996	1
1997	1
1998	2
1999	4
2000	3
2001	6
2002	2
2003	5
2004	6
2005	16
2006	13
2007	7
2008	7
2009	7
2010	3
2011	1
2012	1
2014	2
2015	2
2016	1
2019	1
2021	1
2024	0

1

Polymorphisms in the mannose binding lectin gene affect the cystic fibrosis pulmonary phenotype.

Yarden J, Radojkovic D, De Boeck K, Macek M Jr, Zemkova D, Vavrova V, Vlietinck R, Cassiman JJ, Cuppens H. Yarden J, et al. J Med Genet. 2004 Aug;41(8):629-33. doi: 10.1136/jmg.2003.017947. J Med Genet. 2004. PMID: 15286159 Free PMC article. No abstract available.

2

An MBL2 haplotype and ABCB4 variants modulate the risk of liver disease in cystic fibrosis patients: a multicentre study.

Tomaiuolo R, Degiorgio D, Coviello DA, Baccarelli A, Elce A, Raia V, Motta V, Seia M, Castaldo G, Colombo C. Tomaiuolo R, et al. Dig Liver Dis. 2009 Nov;41(11):817-22. doi: 10.1016/j.dld.2009.03.012. Epub 2009 May 20. Dig Liver Dis. 2009. PMID: 19467940

3

Mannose-binding lectin gene as a modifier of the cystic fibrosis phenotype in Argentinean pediatric patients.

Gravina LP, Crespo C, Giugno H, Sen L, Chertkoff L, Mangano A, Castaños C. Gravina LP, et al. J Cyst Fibros. 2015 Jan;14(1):78-83. doi: 10.1016/j.jcf.2014.07.012. Epub 2014 Aug 29. J Cyst Fibros. 2015. PMID: 25178872 Free article.

4

MBL2 polymorphisms screening in a regional Italian CF Center.

Trevisiol C, Boniotto M, Giglio L, Poli F, Morgutti M, Crovella S. Trevisiol C, et al. J Cyst Fibros. 2005 Sep;4(3):189-91. doi: 10.1016/j.jcf.2005.04.001. J Cyst Fibros. 2005. PMID: 16046196 Free article.

5

[Modifier genes and cystic fibrosis].

Corvol H, Flamant C, Vallet C, Clement A, Brouard J. Corvol H, et al. Arch Pediatr. 2006 Jan;13(1):57-63. doi: 10.1016/j.arcped.2005.09.029. Epub 2005 Nov 7. Arch Pediatr. 2006. PMID: 16274977 Review. French.

6

Modifier genes in cystic fibrosis.

Davies JC, Griesenbach U, Alton E. Davies JC, et al. Pediatr Pulmonol. 2005 May;39(5):383-91. doi: 10.1002/ppul.20198. Pediatr Pulmonol. 2005. PMID: 15765543 Review.

7

Modifier effect of the Toll-like receptor 4 D299G polymorphism in children with cystic fibrosis.

Urquhart DS, Allen J, Elrayess M, Fidler K, Klein N, Jaffé A. Urquhart DS, et al. Arch Immunol Ther Exp (Warsz). 2006 Jul-Aug;54(4):271-6. doi: 10.1007/s00005-006-0029-8. Epub 2006 Jul 10. Arch Immunol Ther Exp (Warsz). 2006. PMID: 16830219 Free article.

8

Airway plumbing.

Hanrahan JW. Hanrahan JW. J Clin Invest. 2000 May;105(10):1343-4. doi: 10.1172/JCI10088. J Clin Invest. 2000. PMID: 10811841 Free PMC article. Review. No abstract available.

9

Homozygosity for L997F in a child with normal clinical and chloride secretory phenotype provides evidence that this cystic fibrosis transmembrane conductance regulator mutation does not cause cystic fibrosis.

Derichs N, Schuster A, Grund I, Ernsting A, Stolpe C, Körtge-Jung S, Gallati S, Stuhrmann M, Kozlowski P, Ballmann M. Derichs N, et al. Clin Genet. 2005 Jun;67(6):529-31. doi: 10.1111/j.1399-0004.2005.00437.x. Clin Genet. 2005. PMID: 15857421 No abstract available.

10

[Genotype and phenotype of gastrointestinal symptoms analysis in children with cystic fibrosis].

Iwańczak F, Smigiel R, Stawarski A, Pawłowicz J, Stembalska A, Mowszet K, Sasiadek M. Iwańczak F, et al. Pol Merkur Lekarski. 2005 Feb;18(104):205-9. Pol Merkur Lekarski. 2005. PMID: 17877132 Polish.

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