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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1939 1
1941 1
1942 2
1945 2
1946 17
1947 5
1948 17
1949 19
1950 34
1951 31
1952 25
1953 28
1954 19
1955 32
1956 54
1957 58
1958 53
1959 86
1960 61
1961 91
1962 106
1963 141
1964 157
1965 153
1966 126
1967 190
1968 213
1969 210
1970 282
1971 212
1972 237
1973 262
1974 255
1975 246
1976 304
1977 262
1978 280
1979 336
1980 335
1981 323
1982 360
1983 400
1984 404
1985 471
1986 521
1987 516
1988 614
1989 657
1990 786
1991 836
1992 917
1993 867
1994 956
1995 1038
1996 1050
1997 1040
1998 1026
1999 1097
2000 1187
2001 1242
2002 1282
2003 1265
2004 1300
2005 1426
2006 1439
2007 1486
2008 1535
2009 1577
2010 1811
2011 1878
2012 2022
2013 2128
2014 2258
2015 2347
2016 2390
2017 2333
2018 2490
2019 2528
2020 2917
2021 3098
2022 2932
2023 2470
2024 13

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Search Results

60,816 results

Results by year

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Page 1
What Is Cystic Fibrosis?
Endres TM, Konstan MW. Endres TM, et al. JAMA. 2022 Jan 11;327(2):191. doi: 10.1001/jama.2021.23280. JAMA. 2022. PMID: 35015036 No abstract available.
Cystic fibrosis.
O'Sullivan BP, Freedman SD. O'Sullivan BP, et al. Lancet. 2009 May 30;373(9678):1891-904. doi: 10.1016/S0140-6736(09)60327-5. Epub 2009 May 4. Lancet. 2009. PMID: 19403164 Review.
Cystic fibrosis is the most common lethal genetic disease in white populations. ...Researchers now have a more complete understanding of the molecular-biological defect that underlies cystic fibrosis, which is leading to new approaches to treatment. ..
Cystic fibrosis is the most common lethal genetic disease in white populations. ...Researchers now have a more complete unders
Cystic Fibrosis.
Grasemann H, Ratjen F. Grasemann H, et al. N Engl J Med. 2023 Nov 2;389(18):1693-1707. doi: 10.1056/NEJMra2216474. N Engl J Med. 2023. PMID: 37913507 Review. No abstract available.
Origins of cystic fibrosis lung disease.
Stoltz DA, Meyerholz DK, Welsh MJ. Stoltz DA, et al. N Engl J Med. 2015 Jan 22;372(4):351-62. doi: 10.1056/NEJMra1300109. N Engl J Med. 2015. PMID: 25607428 Free PMC article. Review. No abstract available.
Cystic fibrosis.
Rowe SM, Miller S, Sorscher EJ. Rowe SM, et al. N Engl J Med. 2005 May 12;352(19):1992-2001. doi: 10.1056/NEJMra043184. N Engl J Med. 2005. PMID: 15888700 No abstract available.
Cystic fibrosis.
Aitken ML. Aitken ML. Curr Opin Pulm Med. 1995 Nov;1(6):425-34. Curr Opin Pulm Med. 1995. PMID: 9363078 Review.
The discussion includes how the cystic fibrosis gene product, the cystic fibrosis transmembrane conductance regulator, produces lung disease; the relationship between genotype and phenotype; the factors that determine prognosis in cystic fibr
The discussion includes how the cystic fibrosis gene product, the cystic fibrosis transmembrane conductance regu …
Cystic fibrosis year in review 2017.
Savant AP, McColley SA. Savant AP, et al. Pediatr Pulmonol. 2018 Sep;53(9):1307-1317. doi: 10.1002/ppul.24081. Epub 2018 Jun 21. Pediatr Pulmonol. 2018. PMID: 29927544 Review.
In this article, we highlight cystic fibrosis (CF) reports published in Pediatric Pulmonology during 2017. ...
In this article, we highlight cystic fibrosis (CF) reports published in Pediatric Pulmonology during 2017. ...
Cystic fibrosis.
Ratjen F, Döring G. Ratjen F, et al. Lancet. 2003 Feb 22;361(9358):681-9. doi: 10.1016/S0140-6736(03)12567-6. Lancet. 2003. PMID: 12606185 Review.
Cystic fibrosis is the most common autosomal recessive disorder in white people, with a frequency of about 1 in 2500 livebirths. ...Gene replacement therapy is still far from being used in patients with cystic fibrosis, mostly because of difficulties o
Cystic fibrosis is the most common autosomal recessive disorder in white people, with a frequency of about 1 in 2500 livebirth
Cystic Fibrosis: Translating Molecular Mechanisms into Effective Therapies.
Jennings MT, Flume PA. Jennings MT, et al. Ann Am Thorac Soc. 2018 Aug;15(8):897-902. doi: 10.1513/AnnalsATS.201802-075FR. Ann Am Thorac Soc. 2018. PMID: 29812963 Free PMC article. Review.
The identification of the cystic fibrosis gene and the advancement of our understanding of the resultant cystic fibrosis transmembrane conductance regulator protein have led to the development of a new class of cystic fibrosis therapies d …
The identification of the cystic fibrosis gene and the advancement of our understanding of the resultant cystic fibr
Cystic fibrosis.
Davies JC, Alton EW, Bush A. Davies JC, et al. BMJ. 2007 Dec 15;335(7632):1255-9. doi: 10.1136/bmj.39391.713229.AD. BMJ. 2007. PMID: 18079549 Free PMC article. Review. No abstract available.
60,816 results
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