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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 655
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 1440
2007 1486
2008 1535
2009 1577
2010 1811
2011 1877
2012 2022
2013 2127
2014 2257
2015 2339
2016 2390
2017 2333
2018 2490
2019 2528
2020 2918
2021 3094
2022 1281
Text availability
Article attribute
Article type
Publication date

Search Results

57,126 results
Results by year
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Page 1
Cystic fibrosis.
Elborn JS. Elborn JS. Lancet. 2016 Nov 19;388(10059):2519-2531. doi: 10.1016/S0140-6736(16)00576-6. Epub 2016 Apr 29. Lancet. 2016. PMID: 27140670 Review.
Cystic fibrosis is a common life-limiting autosomal recessive genetic disorder, with highest prevalence in Europe, North America, and Australia. ...Further small molecule and gene-based therapies are being developed to restore CFTR function; these therapies promise
Cystic fibrosis is a common life-limiting autosomal recessive genetic disorder, with highest prevalence in Europe, North Ameri
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 from the gastroenterologist's perspective.
Ooi CY, Durie PR. Ooi CY, et al. Nat Rev Gastroenterol Hepatol. 2016 Mar;13(3):175-85. doi: 10.1038/nrgastro.2015.226. Epub 2016 Jan 21. Nat Rev Gastroenterol Hepatol. 2016. PMID: 26790364 Review.
Cystic fibrosis is a life-limiting, recessive disease caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. ...Adult patients with cystic fibrosis also have an increased risk of malignancy in the gast
Cystic fibrosis is a life-limiting, recessive disease caused by mutations in the cystic fibrosis transmembrane c
[Historical compilation of cystic fibrosis].
Navarro S. Navarro S. Gastroenterol Hepatol. 2016 Jan;39(1):36-42. doi: 10.1016/j.gastrohep.2015.04.012. Epub 2015 Jun 10. Gastroenterol Hepatol. 2016. PMID: 26070393 Review. Spanish.
Cystic fibrosis is the most common life-shortening recessively inherited disorder in the Caucasian population. The genetic mutation that most frequently provokes cystic fibrosis (deltaF508) appeared at least 53,000years ago. For many centuries, the dis
Cystic fibrosis is the most common life-shortening recessively inherited disorder in the Caucasian population. The genetic mut
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: a clinical view.
Castellani C, Assael BM. Castellani C, et al. Cell Mol Life Sci. 2017 Jan;74(1):129-140. doi: 10.1007/s00018-016-2393-9. Epub 2016 Oct 5. Cell Mol Life Sci. 2017. PMID: 27709245 Review.
Cystic fibrosis (CF), a monogenic disease caused by mutations in the CFTR gene on chromosome 7, is complex and greatly variable in clinical expression. ...
Cystic fibrosis (CF), a monogenic disease caused by mutations in the CFTR gene on chromosome 7, is complex and greatly variabl
Cystic fibrosis year in review 2016.
Savant AP, McColley SA. Savant AP, et al. Pediatr Pulmonol. 2017 Aug;52(8):1092-1102. doi: 10.1002/ppul.23747. Epub 2017 Jun 13. Pediatr Pulmonol. 2017. PMID: 28608632 Review.
In this article, we highlight cystic fibrosis (CF) research and case reports published in Pediatric Pulmonology during 2016. ...
In this article, we highlight cystic fibrosis (CF) research and case reports published in Pediatric Pulmonology during 2016. . …
Cystic fibrosis.
Paranjape SM, Mogayzel PJ Jr. Paranjape SM, et al. Pediatr Rev. 2014 May;35(5):194-205. doi: 10.1542/pir.35-5-194. Pediatr Rev. 2014. PMID: 24790073 No abstract available.
Cystic fibrosis year in review 2018, part 1.
Savant AP, McColley SA. Savant AP, et al. Pediatr Pulmonol. 2019 Aug;54(8):1117-1128. doi: 10.1002/ppul.24361. Epub 2019 May 20. Pediatr Pulmonol. 2019. PMID: 31106528 Review.
Cystic fibrosis research and case reports were robust in the year 2018. This report summarizes research and cases related to Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) modulator therapies, inflammation and infection, epidemiology and th
Cystic fibrosis research and case reports were robust in the year 2018. This report summarizes research and cases related to
The Microbiome in Cystic Fibrosis Pulmonary Disease.
Françoise A, Héry-Arnaud G. Françoise A, et al. Genes (Basel). 2020 May 11;11(5):536. doi: 10.3390/genes11050536. Genes (Basel). 2020. PMID: 32403302 Free PMC article. Review.
Cystic fibrosis (CF) is a genetic disease with mutational changes leading to profound dysbiosis, both pulmonary and intestinal, from a very young age. ...Description of pathological microbiomes and correlation with clinical status and therapeutics (antibiotic therap
Cystic fibrosis (CF) is a genetic disease with mutational changes leading to profound dysbiosis, both pulmonary and intestinal
57,126 results
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