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

Year Number of Results
1946 1
1950 2
1956 1
1958 1
1959 1
1964 2
1965 4
1966 2
1967 1
1968 6
1969 4
1970 10
1971 5
1972 8
1973 13
1974 10
1975 32
1976 29
1977 31
1978 41
1979 39
1980 44
1981 51
1982 49
1983 55
1984 70
1985 92
1986 84
1987 91
1988 124
1989 100
1990 143
1991 130
1992 167
1993 166
1994 206
1995 185
1996 189
1997 245
1998 219
1999 249
2000 253
2001 280
2002 260
2003 319
2004 320
2005 391
2006 336
2007 374
2008 404
2009 417
2010 483
2011 513
2012 562
2013 620
2014 676
2015 695
2016 639
2017 660
2018 729
2019 717
2020 799
2021 882
2022 771
2023 647
2024 255

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14,017 results

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Page 1
Clinical Phenotypes of Cystic Fibrosis Carriers.
Polgreen PM, Comellas AP. Polgreen PM, et al. Annu Rev Med. 2022 Jan 27;73:563-574. doi: 10.1146/annurev-med-042120-020148. Annu Rev Med. 2022. PMID: 35084992 Free PMC article. Review.
Cystic fibrosis (CF) is an autosomal recessive genetic disorder caused by mutations in CFTR, the cystic fibrosis transmembrane conductance regulator gene. ...
Cystic fibrosis (CF) is an autosomal recessive genetic disorder caused by mutations in CFTR, the cystic fibrosis …
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. …
Non-cystic fibrosis bronchiectasis.
Neves PC, Guerra M, Ponce P, Miranda J, Vouga L. Neves PC, et al. Interact Cardiovasc Thorac Surg. 2011 Dec;13(6):619-25. doi: 10.1510/icvts.2011.284208. Epub 2011 Oct 6. Interact Cardiovasc Thorac Surg. 2011. PMID: 21979982 Review.
Exercise or inspiratory muscle training may improve quality of life and exercise endurance in people with non-cystic fibrosis bronchiectasis. Prolonged-use antibiotics improve clinical response rates, but may not reduce exacerbation rates or lung function. Surgery i …
Exercise or inspiratory muscle training may improve quality of life and exercise endurance in people with non-cystic fibrosis …
CYSTIC FIBROSIS.
ASAY LD. ASAY LD. Calif Med. 1965 Apr;102(4):292-300. Calif Med. 1965. PMID: 14288148 Free PMC article. Review.
Cystic fibrosis, a disease thought to be transmitted as a recessive genetic trait, is found as a disease in about one in 1,000 to one in 10,000 births. ...
Cystic fibrosis, a disease thought to be transmitted as a recessive genetic trait, is found as a disease in about one in 1,000 …
Pulmonary Complications of Cystic Fibrosis.
Garcia B, Flume PA. Garcia B, et al. Semin Respir Crit Care Med. 2019 Dec;40(6):804-809. doi: 10.1055/s-0039-1697639. Epub 2019 Oct 28. Semin Respir Crit Care Med. 2019. PMID: 31659729 Review.
Cystic fibrosis (CF) lung disease is characterized by the development of progressive bronchiectasis and impaired lung function with severe airflow obstruction. ...
Cystic fibrosis (CF) lung disease is characterized by the development of progressive bronchiectasis and impaired lung function …
Nutritional Issues in Cystic Fibrosis.
Solomon M, Bozic M, Mascarenhas MR. Solomon M, et al. Clin Chest Med. 2016 Mar;37(1):97-107. doi: 10.1016/j.ccm.2015.11.009. Epub 2015 Dec 24. Clin Chest Med. 2016. PMID: 26857771 Review.
The importance of maintaining adequate nutrition in patients with cystic fibrosis has been well known for the past 3 decades. Achieving normal growth and maintaining optimal nutrition is associated with improved lung function. ...Nutritional management is crucial at …
The importance of maintaining adequate nutrition in patients with cystic fibrosis has been well known for the past 3 decades. …
Telemedicine and cystic fibrosis: Do we still need face-to-face clinics?
Dixon E, Dick K, Ollosson S, Jones D, Mattock H, Bentley S, Saunders C, Matthews J, Dobra B, King J, Edmondson C, Davies JC. Dixon E, et al. Paediatr Respir Rev. 2022 Jun;42:23-28. doi: 10.1016/j.prrv.2021.05.002. Epub 2021 May 19. Paediatr Respir Rev. 2022. PMID: 34215541 Review.
There has been growing interest in telemedicine for cystic fibrosis over recent years based largely on convenience for patients and/or increasing the frequency of surveillance and early detection which, it is assumed, could improve treatment outcomes. ...
There has been growing interest in telemedicine for cystic fibrosis over recent years based largely on convenience for patient …
Prevention of osteoporosis in cystic fibrosis.
Chedevergne F, Sermet-Gaudelus I. Chedevergne F, et al. Curr Opin Pulm Med. 2019 Nov;25(6):660-665. doi: 10.1097/MCP.0000000000000624. Curr Opin Pulm Med. 2019. PMID: 31567515 Review.
PURPOSE OF REVIEW: The increased life span of patients with cystic fibrosis has lead to the detection of new complications. Osteopenia is present in up to 50% of adult patients with cystic fibrosis, and osteoporosis in 10-34% and can cause a difficult …
PURPOSE OF REVIEW: The increased life span of patients with cystic fibrosis has lead to the detection of new complications. Os …
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 …
Lung Transplantation for Cystic Fibrosis.
Morrell MR, Pilewski JM. Morrell MR, et al. Clin Chest Med. 2016 Mar;37(1):127-38. doi: 10.1016/j.ccm.2015.11.008. Clin Chest Med. 2016. PMID: 26857774 Review.
Lung transplantation is a viable option for many patients with cystic fibrosis (CF) and end-stage lung disease. Criteria for transplant in patients with CF vary widely among transplant centers in terms of acceptable comorbidities; referral to multiple centers may be …
Lung transplantation is a viable option for many patients with cystic fibrosis (CF) and end-stage lung disease. Criteria for t …
14,017 results
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