Academic literature on the topic 'Cystic fibrosis'
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Journal articles on the topic "Cystic fibrosis"
Marin, Angelica-Cristina, Dana-Teodora Anton-Păduraru, Nicoleta-Bianca Cloşcă, Doina Mihăilă, and Marin Burlea. "Cystic fibrosis and Helicobacter pylori infection." Romanian Journal of Infectious Diseases 19, no. 2 (June 30, 2016): 54–59. http://dx.doi.org/10.37897/rjid.2016.2.2.
Full textJones, Andrew. "Cystic Fibrosis and Non-Cystic Fibrosis Bronchiectasis." Seminars in Respiratory and Critical Care Medicine 36, no. 02 (March 31, 2015): 167–68. http://dx.doi.org/10.1055/s-0035-1547317.
Full text&NA;. "Cystic fibrosis and fibrosing colonopathy." Advances in Anatomic Pathology 3, no. 2 (March 1996): 112. http://dx.doi.org/10.1097/00125480-199603000-00015.
Full textSmyth, R. L. "Fibrosing colonopathy in cystic fibrosis." Archives of Disease in Childhood 74, no. 5 (May 1, 1996): 464–68. http://dx.doi.org/10.1136/adc.74.5.464.
Full textLYON, IAN C. T., and DIANNE R. WEBSTER. "Newborn Screening for Cystic Fibrosis." Pediatrics 87, no. 6 (June 1, 1991): 954–55. http://dx.doi.org/10.1542/peds.87.6.954.
Full textGrody, Wayne W. "Cystic Fibrosis." Archives of Pathology & Laboratory Medicine 123, no. 11 (November 1, 1999): 1041–46. http://dx.doi.org/10.5858/1999-123-1041-cf.
Full textWendekier, Camille, and Katheryn Wendekier-Raybuck. "Cystic fibrosis." Nursing 51, no. 6 (June 2021): 32–38. http://dx.doi.org/10.1097/01.nurse.0000751344.57701.75.
Full textDavis, P. B. "Cystic Fibrosis." Pediatrics in Review 22, no. 8 (August 1, 2001): 257–64. http://dx.doi.org/10.1542/pir.22-8-257.
Full textMontgomery, G. S., and M. Howenstine. "Cystic Fibrosis." Pediatrics in Review 30, no. 8 (July 31, 2009): 302–10. http://dx.doi.org/10.1542/pir.30-8-302.
Full textParanjape, S. M., and P. J. Mogayzel. "Cystic Fibrosis." Pediatrics in Review 35, no. 5 (May 1, 2014): 194–205. http://dx.doi.org/10.1542/pir.35-5-194.
Full textDissertations / Theses on the topic "Cystic fibrosis"
Chadwick, Helen Kay. "Cognitive function in cystic fibrosis and cystic fibrosis related diabetes (CFRD)." Thesis, University of Leeds, 2016. http://etheses.whiterose.ac.uk/16912/.
Full textKahre, Tiina. "Cystic fibrosis in Estonia /." Online version, 2004. http://dspace.utlib.ee/dspace/bitstream/10062/577/5/KahrePhD.pdf.
Full textDwyer, Tiffany Jane. "Exercise in cystic fibrosis." Thesis, The University of Sydney, 2010. http://hdl.handle.net/2123/6349.
Full textDwyer, Tiffany Jane. "Exercise in cystic fibrosis." Discipline of Physiotherapy, Faculty of Health Sciences, University of Sydney, 2010. http://hdl.handle.net/2123/6349.
Full textExercise and physical activity have many benefits for adults with cystic fibrosis (CF), including the potential to aid mucus clearance, improve lung function, exercise capacity and quality of life. Despite the recommendations from consensus documents for CF adults to engage in regular physical activity, exercise participation amongst this population is often very low. No in-depth study has been undertaken to explore the determinants of exercise participation for this group and no studies have examined the benefits of habitual physical activity on the health status and quality of life of CF adults. As well, the current methods to quantify physical activity are problematic. The series of studies, involving CF adults, in this thesis was therefore undertaken in order to examine the physiological rationale for the use of exercise as an airway clearance technique, to understand the decision making process to engage in exercise, to determine if health status and quality of life were affected by exercise participation, and to establish the accuracy of a recently-developed objective measure of physical activity. The study in Chapter 2 provided some physiological rationale for choosing treadmill exercise to aid airway clearance in CF. The main findings were that a single bout of moderate intensity exercise increased the subjective ease of expectoration, most likely due to the increased ventilation with exercise, and that sputum viscoelasticity was favourably decreased immediately following treadmill exercise compared to cycle exercise and control. The studies in Chapters 3 and 4 identified the main beliefs regarding exercise for CF adults and highlighted that the main predictors of exercise intention and participation for this group were aspects of perceived and actual control to exercise, namely self-efficacy or confidence to exercise, feeling healthy, receiving encouragement to exercise, and rating exercise as a high priority treatment. Positive ratings of these aspects of control either increased exercise participation directly, indirectly by increasing intention, or strengthened the conversion of exercise intention to participation. Strategies aimed at targeting these aspects of control are therefore likely to be effective in increasing exercise participation for CF adults. The study in Chapter 5 demonstrated that CF adults, who reportedly performed at least 90 minutes of moderate to strenuous exercise per week, had significantly higher quality of life and fewer days in hospital over the following year than their peers, who exercised less. The difference in hospitalisation between the CF adults, who reportedly exercised more than 90 minutes per week and those who did not, was independent of baseline lung function, and the females who reportedly performed less than 90 minutes of exercise per week had three times as many days in hospital than their high-activity peers. The study in Chapter 6 showed that the SenseWear Pro3 Armband activity monitor provided a reasonable estimate of energy expenditure and step count. Also, its accuracy was not affected by diagnosis with CF, despite the potential for the high salt content in the sweat to interfere with the device’s physiological sensors placed on the skin. Overall, this series of studies adds to the growing evidence of the physical and psychological benefits from exercise participation for CF adults, as well as providing some empirical evidence upon which to base strategies to improve exercise participation for this group and support for an objective measure of physical activity.
Utley, Courtney, and Kristen L. McHenry. "Advances in Cystic Fibrosis." Digital Commons @ East Tennessee State University, 2016. https://dc.etsu.edu/etsu-works/2546.
Full textDobson, Lee. "Glucose tolerance in cystic fibrosis." Thesis, University of Exeter, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.403679.
Full textHurley, Matthew. "Lung infection in cystic fibrosis." Thesis, University of Nottingham, 2016. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.716679.
Full textDowney, D. G. "Airways inflammation in cystic fibrosis." Thesis, Queen's University Belfast, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.269047.
Full textEvans, Katharine Sarah Emily. "Cystic Fibrosis and the eye." Thesis, Cardiff University, 2009. http://orca.cf.ac.uk/54848/.
Full textWright, Adam. "The macrophage in cystic fibrosis." Thesis, University of Leicester, 2007. http://hdl.handle.net/2381/8783.
Full textBooks on the topic "Cystic fibrosis"
Silverstein, Alvin. Cystic fibrosis. New York: F. Watts, 1994.
Find full textDavis, Stephanie Duggins, Margaret Rosenfeld, and James Chmiel, eds. Cystic Fibrosis. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-42382-7.
Full textMoss, Richard B., ed. Cystic Fibrosis. Totowa, NJ: Humana Press, 1990. http://dx.doi.org/10.1007/978-1-4612-0475-6.
Full textAmaral, Margarida D., and Karl Kunzelmann, eds. Cystic Fibrosis. Totowa, NJ: Humana Press, 2011. http://dx.doi.org/10.1007/978-1-61779-117-8.
Full textAmaral, Margarida D., and Karl Kunzelmann, eds. Cystic Fibrosis. Totowa, NJ: Humana Press, 2011. http://dx.doi.org/10.1007/978-1-61779-120-8.
Full textGold, Susan Dudley. Cystic fibrosis. New York: Crestwood House, 2000.
Find full textB, Davis Pamela, ed. Cystic fibrosis. New York: M. Dekker, 1993.
Find full text1951-, Goodfellow P., ed. Cystic fibrosis. Oxford: Oxford University Press, 1989.
Find full textB, Fiel Stanley, ed. Cystic fibrosis. Philadelphia: Saunders, 1998.
Find full textE, Hodson Margaret, Geddes Duncan M, and Bush, Andrew, 1954 Apr. 24-, eds. Cystic fibrosis. 3rd ed. London: Hodder Arnold, 2007.
Find full textBook chapters on the topic "Cystic fibrosis"
Moss, Richard B. "Introduction." In Cystic Fibrosis, v—ix. Totowa, NJ: Humana Press, 1990. http://dx.doi.org/10.1007/978-1-4612-0475-6_1.
Full textTepper, Robert S., and Howard Eigen. "Airway Reactivity in Cystic Fibrosis." In Cystic Fibrosis, 159–68. Totowa, NJ: Humana Press, 1990. http://dx.doi.org/10.1007/978-1-4612-0475-6_10.
Full textSpino, Michael. "Pharmacokinetics of Drugs in Cystic Fibrosis." In Cystic Fibrosis, 169–210. Totowa, NJ: Humana Press, 1990. http://dx.doi.org/10.1007/978-1-4612-0475-6_11.
Full textMoss, Richard B. "Drug Allergy in Cystic Fibrosis." In Cystic Fibrosis, 211–29. Totowa, NJ: Humana Press, 1990. http://dx.doi.org/10.1007/978-1-4612-0475-6_12.
Full textLewiston, Norman, Vaughn Starnes, and James Theodore. "Heart-Lung and Lung Transplantation for Cystic Fibrosis." In Cystic Fibrosis, 231–47. Totowa, NJ: Humana Press, 1990. http://dx.doi.org/10.1007/978-1-4612-0475-6_13.
Full textWine, Jeffrey J. "Basic Aspects of Cystic Fibrosis." In Cystic Fibrosis, 1–28. Totowa, NJ: Humana Press, 1990. http://dx.doi.org/10.1007/978-1-4612-0475-6_2.
Full textWilmott, Robert W. "The Relationship Between Atopy and Cystic Fibrosis." In Cystic Fibrosis, 29–46. Totowa, NJ: Humana Press, 1990. http://dx.doi.org/10.1007/978-1-4612-0475-6_3.
Full textSorensen, Ricardo U., Robert L. Waller, and Jeffrey D. Klinger. "Infection and Immunity to Pseudomonas." In Cystic Fibrosis, 47–74. Totowa, NJ: Humana Press, 1990. http://dx.doi.org/10.1007/978-1-4612-0475-6_4.
Full textGreenberg, David P., and Harris R. Stutman. "Infection and Immunity to Staphylococcus aureus and Haemophilus influenzae." In Cystic Fibrosis, 75–86. Totowa, NJ: Humana Press, 1990. http://dx.doi.org/10.1007/978-1-4612-0475-6_5.
Full textProber, Charles G. "The Impact of Respiratory Viral Infections in Patients with Cystic Fibrosis." In Cystic Fibrosis, 87–102. Totowa, NJ: Humana Press, 1990. http://dx.doi.org/10.1007/978-1-4612-0475-6_6.
Full textConference papers on the topic "Cystic fibrosis"
Škrbic, Dusan, Mirna Djuric, Jelena Papovic, and Branislav Tusek. "COVID-19 vaccine and morbidity in the Adult Cystic Fibrosis Centre in Institute for Pulmonary Diseases of Vojvodina Sremska Kamenica, Serbia." In Adult Cystic Fibrosis Conference abstracts. European Respiratory Society, 2023. http://dx.doi.org/10.1183/23120541.acf-2023.47.
Full textPetrova, Guergana, Mila Baycheva, Dimitrinka Miteva, Vera Papochieva, Margarita Nikolova, Miglena Georgieva, Nadezhda Yaneva, and Savov Alexey. "Late diagnosed homozygous delF508 patients - is it really rare?" In Adult Cystic Fibrosis Conference abstracts. European Respiratory Society, 2023. http://dx.doi.org/10.1183/23120541.acf-2023.2.
Full textRemus, Natascha, Gaetan Leignadier, Elisa Thomas, Celine Delestrain, Michael Shum, Bernard Maitre, Ralph Epaud, and Benoit Douvry. "The A-Step - a new incremental exercise test defying space and infection control measures." In Adult Cystic Fibrosis Conference abstracts. European Respiratory Society, 2023. http://dx.doi.org/10.1183/23120541.acf-2023.17.
Full textDuplacie, Nele, Trudy Havermans, Janne Houben, Marianne Schulte, Linda Boulanger, Laura Moyens, Cindy Ruelens, and Lieven Dupont. "Side-effects and ETI-treatment: a multidisciplinary challenge." In Adult Cystic Fibrosis Conference abstracts. European Respiratory Society, 2023. http://dx.doi.org/10.1183/23120541.acf-2023.37.
Full textDaniels, Tanne, Kristel Van Calsteren, and Lieven Dupont. "Maternal and obstetric outcomes in women with cystic fibrosis: a retrospective case series of patients in UZ Leuven." In Adult Cystic Fibrosis Conference abstracts. European Respiratory Society, 2023. http://dx.doi.org/10.1183/23120541.acf-2023.31.
Full textSkogeland, Ulrika, Anna Hedborg, Cecilia Rodriguez, Adrienn Bánki, and Tove Godskesen. "Adherence to medical regimens after lung transplantation among adults with Cystic Fibrosis increased during COVID-19 pandemic." In Adult Cystic Fibrosis Conference abstracts. European Respiratory Society, 2023. http://dx.doi.org/10.1183/23120541.acf-2023.4.
Full textAsir, Nadine, Noor Al-Sulaiti, Abdusamea Shabani, and Atqah Abdul Wahab. "First case of pott's disease in a cystic fibrosis adolescent with a homozygous CFTR mutation c.3700 A > G (p. Ile1234Val)." In Adult Cystic Fibrosis Conference abstracts. European Respiratory Society, 2023. http://dx.doi.org/10.1183/23120541.acf-2023.29.
Full textMomchilovikj, Sonja, Dejan Dokic, Sava Pejkovska, Smiljko Jovanoski, Dimitar Karkinski, Zoran Arsovski, Stojka Naceva-Fustik, et al. "Initial experiences in treatment with modulatory therapy in patients with Cystic Fibrosis in North Macedonia." In Adult Cystic Fibrosis Conference abstracts. European Respiratory Society, 2023. http://dx.doi.org/10.1183/23120541.acf-2023.39.
Full textBaxter, Gabrielle, Ashkan Pakzad, Bojidar Rangelov, Shayan Shaikh, Ying Xin Tan, Robert Chapman, Daniel Peckham, and Joseph Jacob. "Quantitative computed tomography measures of disease severity in cystic fibrosis." In Adult Cystic Fibrosis Conference abstracts. European Respiratory Society, 2023. http://dx.doi.org/10.1183/23120541.acf-2023.35.
Full textAlyami, Mohammad Hussain. "Middle east respiratory syndrome (MERS) and novel coronavirus disease-2019 (COVID-19) from causes to preventions in Saudi Arabia." In Adult Cystic Fibrosis Conference abstracts. European Respiratory Society, 2023. http://dx.doi.org/10.1183/23120541.acf-2023.1.
Full textReports on the topic "Cystic fibrosis"
Garber, Alan, and Joseph Fenerty. Costs and Benefits of Prenatal Screening For Cystic Fibrosis. Cambridge, MA: National Bureau of Economic Research, October 1988. http://dx.doi.org/10.3386/w2749.
Full textBarros-Poblete, Marisol, Rodrigo Torres-Castro, Mauricio Henríquez, Anita Guequen, Isabel Blanco, and Carlos Flores. Dysbiosis as a prognostic factor for clinical worsening in chronic respiratory disease: A systematic review and metanalysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, April 2022. http://dx.doi.org/10.37766/inplasy2022.4.0089.
Full textTaub, Daniel, and Joshua Page. Cystic Fibrosis: Exploration of Evolutionary Explanations for the High Frequency of a Common Genetic Disorder. Genetics Society of America Peer-Reviewed Education Portal (GSA PREP), October 2013. http://dx.doi.org/10.1534/gsaprep.2013.004.
Full textBorisova, Dayana, Tanya Strateva, Tsvetelina Paunova-Krasteva, Ivan Mitov, and Stoyanka Stoitsova. Phenotypic Investigation of Paired Pseudomonas aeruginosa Strains Isolated from Cystic Fibrosis Patients Prior- and Post-tobramycin Treatment. "Prof. Marin Drinov" Publishing House of Bulgarian Academy of Sciences, August 2018. http://dx.doi.org/10.7546/crabs.2018.08.05.
Full textJangir, Hemlata, Aparna Ningombam, Arulselvi Subramanian, and Subodh Kumar. Traumatic Jejunal Mesenteric Pseudocyst in the Vicinity of Blunt Abdominal Trauma with a Brief Review of Literature. Science Repository, January 2023. http://dx.doi.org/10.31487/j.ajscr.2022.04.04.
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