Similar articles for PMID: 15857421

Year	Number of Results
1959	1
1960	1
1962	1
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1966	1
1967	1
1968	1
1969	4
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1976	3
1979	2
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1991	5
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1994	1
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2000	11
2001	11
2002	15
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2007	10
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2012	6
2013	6
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2016	10
2017	6
2018	7
2019	9
2020	12
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2023	5
2024	0

1

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.

2

Phenotypic variability in a family with pancreatitis and cystic fibrosis sharing common mild CFTR mutation: report on CFTR mutations and their phenotypic variability.

Alghisi F, Bella S, Lucidi V, Angioni A, Tomaiuolo AC, D'Apice MR, Gambardella S, Novelli G. Alghisi F, et al. Pancreas. 2009 Jan;38(1):109-10. doi: 10.1097/MPA.0b013e3181671b9c. Pancreas. 2009. PMID: 19106752 No abstract available.

3

[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.

4

Glucose homeostasis and genotype-phenotype interplay in cystic fibrosis patients with CFTR gene deltaF508 mutation.

Preumont V, Hermans MP, Lebecque P, Buysschaert M. Preumont V, et al. Diabetes Care. 2007 May;30(5):1187-92. doi: 10.2337/dc06-1915. Epub 2007 Mar 2. Diabetes Care. 2007. PMID: 17337503

5

Sweat chloride concentration in cystic fibrosis patients with cystic fibrosis trans-membrane conductance regulator I1234V mutation.

Abdul-Wahab A, Janahi IA, Abdel-Rahman MO. Abdul-Wahab A, et al. Saudi Med J. 2009 Aug;30(8):1101-2. Saudi Med J. 2009. PMID: 19668897 No abstract available.

6

Nonclassic cystic fibrosis: a clinical conundrum.

Rosenstein BJ. Rosenstein BJ. Pediatr Pulmonol. 2003 Jul;36(1):10-2. doi: 10.1002/ppul.10286. Pediatr Pulmonol. 2003. PMID: 12772217 No abstract available.

7

Cystic fibrosis mutations with widely variable phenotype: the D1152H example.

Mussaffi H, Prais D, Mei-Zahav M, Blau H. Mussaffi H, et al. Pediatr Pulmonol. 2006 Mar;41(3):250-4. doi: 10.1002/ppul.20343. Pediatr Pulmonol. 2006. PMID: 16429425

8

Disease severity associated with cystic fibrosis mutations deltaF508 and S549R(T-->G).

Dawson KP, Frossard PM, Al-Awar B. Dawson KP, et al. East Mediterr Health J. 2001 Nov;7(6):975-80. East Mediterr Health J. 2001. PMID: 15332739 Free article.

9

A novel nonsense mutation, S466Xa in exon 10 of the cystic fibrosis transmembrane conductance regulator gene.

Mittre H, Barre M, Leymarie P. Mittre H, et al. Hum Mutat. 1996;8(4):392-3. doi: 10.1002/humu.1380080402. Hum Mutat. 1996. PMID: 8956053 No abstract available.

10

Outcome of intracytoplasmic sperm injection for a couple in which the man is carrier of CFTR p.[R74W;V201M;D1270N] and p.P841R mutations and his spouse a heterozygous carrier of p.F508del mutation of the cystic fibrosis transmembrane conductance regulator gene.

Brugnon F, Bilan F, Heraud MC, Grizard G, Janny L, Creveaux I. Brugnon F, et al. Fertil Steril. 2008 Nov;90(5):2004.e23-6. doi: 10.1016/j.fertnstert.2008.05.057. Epub 2008 Aug 13. Fertil Steril. 2008. PMID: 18703181 Free article.

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