Gotowa bibliografia na temat „Cystic fibrosis”
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Artykuły w czasopismach na temat "Cystic fibrosis"
Marin, Angelica-Cristina, Dana-Teodora Anton-Păduraru, Nicoleta-Bianca Cloşcă, Doina Mihăilă i Marin Burlea. "Cystic fibrosis and Helicobacter pylori infection". Romanian Journal of Infectious Diseases 19, nr 2 (30.06.2016): 54–59. http://dx.doi.org/10.37897/rjid.2016.2.2.
Pełny tekst źródłaJones, Andrew. "Cystic Fibrosis and Non-Cystic Fibrosis Bronchiectasis". Seminars in Respiratory and Critical Care Medicine 36, nr 02 (31.03.2015): 167–68. http://dx.doi.org/10.1055/s-0035-1547317.
Pełny tekst źródła&NA;. "Cystic fibrosis and fibrosing colonopathy". Advances in Anatomic Pathology 3, nr 2 (marzec 1996): 112. http://dx.doi.org/10.1097/00125480-199603000-00015.
Pełny tekst źródłaSmyth, R. L. "Fibrosing colonopathy in cystic fibrosis." Archives of Disease in Childhood 74, nr 5 (1.05.1996): 464–68. http://dx.doi.org/10.1136/adc.74.5.464.
Pełny tekst źródłaLYON, IAN C. T., i DIANNE R. WEBSTER. "Newborn Screening for Cystic Fibrosis". Pediatrics 87, nr 6 (1.06.1991): 954–55. http://dx.doi.org/10.1542/peds.87.6.954.
Pełny tekst źródłaGrody, Wayne W. "Cystic Fibrosis". Archives of Pathology & Laboratory Medicine 123, nr 11 (1.11.1999): 1041–46. http://dx.doi.org/10.5858/1999-123-1041-cf.
Pełny tekst źródłaWendekier, Camille, i Katheryn Wendekier-Raybuck. "Cystic fibrosis". Nursing 51, nr 6 (czerwiec 2021): 32–38. http://dx.doi.org/10.1097/01.nurse.0000751344.57701.75.
Pełny tekst źródłaDavis, P. B. "Cystic Fibrosis". Pediatrics in Review 22, nr 8 (1.08.2001): 257–64. http://dx.doi.org/10.1542/pir.22-8-257.
Pełny tekst źródłaMontgomery, G. S., i M. Howenstine. "Cystic Fibrosis". Pediatrics in Review 30, nr 8 (31.07.2009): 302–10. http://dx.doi.org/10.1542/pir.30-8-302.
Pełny tekst źródłaParanjape, S. M., i P. J. Mogayzel. "Cystic Fibrosis". Pediatrics in Review 35, nr 5 (1.05.2014): 194–205. http://dx.doi.org/10.1542/pir.35-5-194.
Pełny tekst źródłaRozprawy doktorskie na temat "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/.
Pełny tekst źródłaKahre, Tiina. "Cystic fibrosis in Estonia /". Online version, 2004. http://dspace.utlib.ee/dspace/bitstream/10062/577/5/KahrePhD.pdf.
Pełny tekst źródłaDwyer, Tiffany Jane. "Exercise in cystic fibrosis". Thesis, The University of Sydney, 2010. http://hdl.handle.net/2123/6349.
Pełny tekst źródłaDwyer, Tiffany Jane. "Exercise in cystic fibrosis". Discipline of Physiotherapy, Faculty of Health Sciences, University of Sydney, 2010. http://hdl.handle.net/2123/6349.
Pełny tekst źródłaExercise 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, i Kristen L. McHenry. "Advances in Cystic Fibrosis". Digital Commons @ East Tennessee State University, 2016. https://dc.etsu.edu/etsu-works/2546.
Pełny tekst źródłaDobson, Lee. "Glucose tolerance in cystic fibrosis". Thesis, University of Exeter, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.403679.
Pełny tekst źródłaHurley, Matthew. "Lung infection in cystic fibrosis". Thesis, University of Nottingham, 2016. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.716679.
Pełny tekst źródłaDowney, D. G. "Airways inflammation in cystic fibrosis". Thesis, Queen's University Belfast, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.269047.
Pełny tekst źródłaEvans, Katharine Sarah Emily. "Cystic Fibrosis and the eye". Thesis, Cardiff University, 2009. http://orca.cf.ac.uk/54848/.
Pełny tekst źródłaWright, Adam. "The macrophage in cystic fibrosis". Thesis, University of Leicester, 2007. http://hdl.handle.net/2381/8783.
Pełny tekst źródłaKsiążki na temat "Cystic fibrosis"
Silverstein, Alvin. Cystic fibrosis. New York: F. Watts, 1994.
Znajdź pełny tekst źródłaDavis, Stephanie Duggins, Margaret Rosenfeld i James Chmiel, red. Cystic Fibrosis. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-42382-7.
Pełny tekst źródłaMoss, Richard B., red. Cystic Fibrosis. Totowa, NJ: Humana Press, 1990. http://dx.doi.org/10.1007/978-1-4612-0475-6.
Pełny tekst źródłaAmaral, Margarida D., i Karl Kunzelmann, red. Cystic Fibrosis. Totowa, NJ: Humana Press, 2011. http://dx.doi.org/10.1007/978-1-61779-117-8.
Pełny tekst źródłaAmaral, Margarida D., i Karl Kunzelmann, red. Cystic Fibrosis. Totowa, NJ: Humana Press, 2011. http://dx.doi.org/10.1007/978-1-61779-120-8.
Pełny tekst źródłaGold, Susan Dudley. Cystic fibrosis. New York: Crestwood House, 2000.
Znajdź pełny tekst źródłaB, Davis Pamela, red. Cystic fibrosis. New York: M. Dekker, 1993.
Znajdź pełny tekst źródła1951-, Goodfellow P., red. Cystic fibrosis. Oxford: Oxford University Press, 1989.
Znajdź pełny tekst źródłaB, Fiel Stanley, red. Cystic fibrosis. Philadelphia: Saunders, 1998.
Znajdź pełny tekst źródłaE, Hodson Margaret, Geddes Duncan M i Bush, Andrew, 1954 Apr. 24-, red. Cystic fibrosis. Wyd. 3. London: Hodder Arnold, 2007.
Znajdź pełny tekst źródłaCzęści książek na temat "Cystic fibrosis"
Moss, Richard B. "Introduction". W Cystic Fibrosis, v—ix. Totowa, NJ: Humana Press, 1990. http://dx.doi.org/10.1007/978-1-4612-0475-6_1.
Pełny tekst źródłaTepper, Robert S., i Howard Eigen. "Airway Reactivity in Cystic Fibrosis". W Cystic Fibrosis, 159–68. Totowa, NJ: Humana Press, 1990. http://dx.doi.org/10.1007/978-1-4612-0475-6_10.
Pełny tekst źródłaSpino, Michael. "Pharmacokinetics of Drugs in Cystic Fibrosis". W Cystic Fibrosis, 169–210. Totowa, NJ: Humana Press, 1990. http://dx.doi.org/10.1007/978-1-4612-0475-6_11.
Pełny tekst źródłaMoss, Richard B. "Drug Allergy in Cystic Fibrosis". W Cystic Fibrosis, 211–29. Totowa, NJ: Humana Press, 1990. http://dx.doi.org/10.1007/978-1-4612-0475-6_12.
Pełny tekst źródłaLewiston, Norman, Vaughn Starnes i James Theodore. "Heart-Lung and Lung Transplantation for Cystic Fibrosis". W Cystic Fibrosis, 231–47. Totowa, NJ: Humana Press, 1990. http://dx.doi.org/10.1007/978-1-4612-0475-6_13.
Pełny tekst źródłaWine, Jeffrey J. "Basic Aspects of Cystic Fibrosis". W Cystic Fibrosis, 1–28. Totowa, NJ: Humana Press, 1990. http://dx.doi.org/10.1007/978-1-4612-0475-6_2.
Pełny tekst źródłaWilmott, Robert W. "The Relationship Between Atopy and Cystic Fibrosis". W Cystic Fibrosis, 29–46. Totowa, NJ: Humana Press, 1990. http://dx.doi.org/10.1007/978-1-4612-0475-6_3.
Pełny tekst źródłaSorensen, Ricardo U., Robert L. Waller i Jeffrey D. Klinger. "Infection and Immunity to Pseudomonas". W Cystic Fibrosis, 47–74. Totowa, NJ: Humana Press, 1990. http://dx.doi.org/10.1007/978-1-4612-0475-6_4.
Pełny tekst źródłaGreenberg, David P., i Harris R. Stutman. "Infection and Immunity to Staphylococcus aureus and Haemophilus influenzae". W Cystic Fibrosis, 75–86. Totowa, NJ: Humana Press, 1990. http://dx.doi.org/10.1007/978-1-4612-0475-6_5.
Pełny tekst źródłaProber, Charles G. "The Impact of Respiratory Viral Infections in Patients with Cystic Fibrosis". W Cystic Fibrosis, 87–102. Totowa, NJ: Humana Press, 1990. http://dx.doi.org/10.1007/978-1-4612-0475-6_6.
Pełny tekst źródłaStreszczenia konferencji na temat "Cystic fibrosis"
Škrbic, Dusan, Mirna Djuric, Jelena Papovic i Branislav Tusek. "COVID-19 vaccine and morbidity in the Adult Cystic Fibrosis Centre in Institute for Pulmonary Diseases of Vojvodina Sremska Kamenica, Serbia". W Adult Cystic Fibrosis Conference abstracts. European Respiratory Society, 2023. http://dx.doi.org/10.1183/23120541.acf-2023.47.
Pełny tekst źródłaPetrova, Guergana, Mila Baycheva, Dimitrinka Miteva, Vera Papochieva, Margarita Nikolova, Miglena Georgieva, Nadezhda Yaneva i Savov Alexey. "Late diagnosed homozygous delF508 patients - is it really rare?" W Adult Cystic Fibrosis Conference abstracts. European Respiratory Society, 2023. http://dx.doi.org/10.1183/23120541.acf-2023.2.
Pełny tekst źródłaRemus, Natascha, Gaetan Leignadier, Elisa Thomas, Celine Delestrain, Michael Shum, Bernard Maitre, Ralph Epaud i Benoit Douvry. "The A-Step - a new incremental exercise test defying space and infection control measures". W Adult Cystic Fibrosis Conference abstracts. European Respiratory Society, 2023. http://dx.doi.org/10.1183/23120541.acf-2023.17.
Pełny tekst źródłaDuplacie, Nele, Trudy Havermans, Janne Houben, Marianne Schulte, Linda Boulanger, Laura Moyens, Cindy Ruelens i Lieven Dupont. "Side-effects and ETI-treatment: a multidisciplinary challenge". W Adult Cystic Fibrosis Conference abstracts. European Respiratory Society, 2023. http://dx.doi.org/10.1183/23120541.acf-2023.37.
Pełny tekst źródłaDaniels, Tanne, Kristel Van Calsteren i Lieven Dupont. "Maternal and obstetric outcomes in women with cystic fibrosis: a retrospective case series of patients in UZ Leuven". W Adult Cystic Fibrosis Conference abstracts. European Respiratory Society, 2023. http://dx.doi.org/10.1183/23120541.acf-2023.31.
Pełny tekst źródłaSkogeland, Ulrika, Anna Hedborg, Cecilia Rodriguez, Adrienn Bánki i Tove Godskesen. "Adherence to medical regimens after lung transplantation among adults with Cystic Fibrosis increased during COVID-19 pandemic". W Adult Cystic Fibrosis Conference abstracts. European Respiratory Society, 2023. http://dx.doi.org/10.1183/23120541.acf-2023.4.
Pełny tekst źródłaAsir, Nadine, Noor Al-Sulaiti, Abdusamea Shabani i 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)". W Adult Cystic Fibrosis Conference abstracts. European Respiratory Society, 2023. http://dx.doi.org/10.1183/23120541.acf-2023.29.
Pełny tekst źródłaMomchilovikj, Sonja, Dejan Dokic, Sava Pejkovska, Smiljko Jovanoski, Dimitar Karkinski, Zoran Arsovski, Stojka Naceva-Fustik i in. "Initial experiences in treatment with modulatory therapy in patients with Cystic Fibrosis in North Macedonia". W Adult Cystic Fibrosis Conference abstracts. European Respiratory Society, 2023. http://dx.doi.org/10.1183/23120541.acf-2023.39.
Pełny tekst źródłaBaxter, Gabrielle, Ashkan Pakzad, Bojidar Rangelov, Shayan Shaikh, Ying Xin Tan, Robert Chapman, Daniel Peckham i Joseph Jacob. "Quantitative computed tomography measures of disease severity in cystic fibrosis". W Adult Cystic Fibrosis Conference abstracts. European Respiratory Society, 2023. http://dx.doi.org/10.1183/23120541.acf-2023.35.
Pełny tekst źródłaAlyami, Mohammad Hussain. "Middle east respiratory syndrome (MERS) and novel coronavirus disease-2019 (COVID-19) from causes to preventions in Saudi Arabia". W Adult Cystic Fibrosis Conference abstracts. European Respiratory Society, 2023. http://dx.doi.org/10.1183/23120541.acf-2023.1.
Pełny tekst źródłaRaporty organizacyjne na temat "Cystic fibrosis"
Garber, Alan, i Joseph Fenerty. Costs and Benefits of Prenatal Screening For Cystic Fibrosis. Cambridge, MA: National Bureau of Economic Research, październik 1988. http://dx.doi.org/10.3386/w2749.
Pełny tekst źródłaBarros-Poblete, Marisol, Rodrigo Torres-Castro, Mauricio Henríquez, Anita Guequen, Isabel Blanco i 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, kwiecień 2022. http://dx.doi.org/10.37766/inplasy2022.4.0089.
Pełny tekst źródłaTaub, Daniel, i 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), październik 2013. http://dx.doi.org/10.1534/gsaprep.2013.004.
Pełny tekst źródłaBorisova, Dayana, Tanya Strateva, Tsvetelina Paunova-Krasteva, Ivan Mitov i 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, sierpień 2018. http://dx.doi.org/10.7546/crabs.2018.08.05.
Pełny tekst źródłaJangir, Hemlata, Aparna Ningombam, Arulselvi Subramanian i Subodh Kumar. Traumatic Jejunal Mesenteric Pseudocyst in the Vicinity of Blunt Abdominal Trauma with a Brief Review of Literature. Science Repository, styczeń 2023. http://dx.doi.org/10.31487/j.ajscr.2022.04.04.
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