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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 814
1991 858
1992 935
1993 894
1994 976
1995 1063
1996 1072
1997 1067
1998 1055
1999 1122
2000 1218
2001 1265
2002 1309
2003 1300
2004 1335
2005 1458
2006 1483
2007 1526
2008 1573
2009 1626
2010 1847
2011 1916
2012 2064
2013 2178
2014 2313
2015 2393
2016 2448
2017 2397
2018 2547
2019 2596
2020 2986
2021 3167
2022 3010
2023 2735
2024 2775
2025 1501
2026 1

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66,141 results

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Page 1
Cystic fibrosis: Epidemiology, clinical manifestations, diagnosis and treatment.
Diab Cáceres L, Zamarrón de Lucas E. Diab Cáceres L, et al. Med Clin (Barc). 2023 Nov 10;161(9):389-396. doi: 10.1016/j.medcli.2023.06.006. Epub 2023 Aug 7. Med Clin (Barc). 2023. PMID: 37558605 Review. English, Spanish.
Until a decade ago, treatments were aimed at favoring secretion drainage, reducing respiratory exacerbations, controlling chronic bronchial infection and slowing functional deterioration, but with the advent of cystic fibrosis transmembrane conductance regulator (CF …
Until a decade ago, treatments were aimed at favoring secretion drainage, reducing respiratory exacerbations, controlling chronic bronchial …
Cystic Fibrosis: Back to the Basics.
Myer H, Chupita S, Jnah A. Myer H, et al. Neonatal Netw. 2023 Jan 1;42(1):23-30. doi: 10.1891/NN-2022-0007. Neonatal Netw. 2023. PMID: 36631257 Review.
Cystic fibrosis (CF) is the most common genetic disorder in Caucasian individuals, with an incidence of 1/2,500-3,500 live births. ...
Cystic fibrosis (CF) is the most common genetic disorder in Caucasian individuals, with an incidence of 1/2,500-3,500 live bir …
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.
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.
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 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 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.
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.
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.
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