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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
1944 1
1945 2
1946 17
1947 6
1948 19
1949 19
1950 34
1951 31
1952 25
1953 29
1954 19
1955 32
1956 54
1957 58
1958 54
1959 87
1960 61
1961 91
1962 107
1963 147
1964 159
1965 154
1966 127
1967 192
1968 215
1969 211
1970 284
1971 214
1972 242
1973 264
1974 256
1975 251
1976 311
1977 269
1978 295
1979 342
1980 347
1981 326
1982 366
1983 414
1984 429
1985 489
1986 539
1987 532
1988 628
1989 671
1990 813
1991 858
1992 935
1993 894
1994 975
1995 1063
1996 1072
1997 1067
1998 1055
1999 1122
2000 1218
2001 1265
2002 1309
2003 1300
2004 1335
2005 1458
2006 1482
2007 1526
2008 1573
2009 1626
2010 1847
2011 1916
2012 2065
2013 2178
2014 2313
2015 2393
2016 2448
2017 2397
2018 2546
2019 2596
2020 2984
2021 3171
2022 3008
2023 2128
2024 1

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61,892 results

Results by year

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Page 1
Cystic fibrosis: current therapeutic targets and future approaches.
Rafeeq MM, Murad HAS. Rafeeq MM, et al. J Transl Med. 2017 Apr 27;15(1):84. doi: 10.1186/s12967-017-1193-9. J Transl Med. 2017. PMID: 28449677 Free PMC article. Review.
OBJECTIVES: Study of currently approved drugs and exploration of future clinical development pipeline therapeutics for cystic fibrosis, and possible limitations in their use. METHODS: Extensive literature search using individual and a combination of key words relate …
OBJECTIVES: Study of currently approved drugs and exploration of future clinical development pipeline therapeutics for cystic fibr …
Cystic fibrosis in the year 2020: A disease with a new face.
De Boeck K. De Boeck K. Acta Paediatr. 2020 May;109(5):893-899. doi: 10.1111/apa.15155. Epub 2020 Jan 22. Acta Paediatr. 2020. PMID: 31899933 Review.
The autosomal recessive disease cystic fibrosis (CF) was once untreatable and deadly in childhood, but now most patients survive to adulthood. ...
The autosomal recessive disease cystic fibrosis (CF) was once untreatable and deadly in childhood, but now most patients survi …
Cystic Fibrosis Revisited - a Review Study.
Klimova B, Kuca K, Novotny M, Maresova P. Klimova B, et al. Med Chem. 2017;13(2):102-109. doi: 10.2174/1573406412666160608113235. Med Chem. 2017. PMID: 27292156 Review.
BACKGROUND: Cystic fibrosis (CF) is an incurable, chronic disease, which causes severe damages to respiratory and digestive tracts. ...This disease is caused by defects in CF genes, the so-called mutations in cystic fibrosis transmembrane conductance r …
BACKGROUND: Cystic fibrosis (CF) is an incurable, chronic disease, which causes severe damages to respiratory and digestive tr …
Cystic fibrosis.
Radlović N. Radlović N. Srp Arh Celok Lek. 2012 Mar-Apr;140(3-4):244-9. Srp Arh Celok Lek. 2012. PMID: 22650116 Free article. Review.
Cystic fibrosis (CF) is a multisystemic autosomal recessive disease caused by a defect in the expression of CFTR protein, i.e. chloride channel present in the apical membrane of respiratory, digestive, reproductive and sweat glands epithelium. ...
Cystic fibrosis (CF) is a multisystemic autosomal recessive disease caused by a defect in the expression of CFTR protein, i.e. …
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 related diabetes: Medical management.
Ode KL, Chan CL, Granados A, Moheet A, Moran A, Brennan AL. Ode KL, et al. J Cyst Fibros. 2019 Oct;18 Suppl 2:S10-S18. doi: 10.1016/j.jcf.2019.08.003. J Cyst Fibros. 2019. PMID: 31679720 Free article. Review.
Cystic Fibrosis Related Diabetes Mellitus (CFRD) drives excess pulmonary morbidity and mortality in patients with cystic fibrosis (CF). ...There is great opportunity for further research to better understand when and how best to treat glycaemic abnorma …
Cystic Fibrosis Related Diabetes Mellitus (CFRD) drives excess pulmonary morbidity and mortality in patients with cystic …
Cystic fibrosis.
David TJ. David TJ. Arch Dis Child. 1990 Jan;65(1):152-7. doi: 10.1136/adc.65.1.152. Arch Dis Child. 1990. PMID: 2405786 Free PMC article. Review. No abstract available.
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 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 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 …
61,892 results
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