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You searched for subject:(cystic fibrosis). Showing records 1 – 30 of 754 total matches.

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University of Hong Kong

1. Chen, Xinying. Regional disturbances by the [delta]F508 mutation on the cystic fibrosis transmembrane conductance regulator.

Degree: PhD, 2016, University of Hong Kong

Cystic fibrosis (CF) is a genetic disease caused by dysfunction of the cystic fibrosis transmemberane conductance regulator (CFTR). The ΔF508 mutation, missing the phenylalanine residue… (more)

Subjects/Keywords: Cystic fibrosis - Pathophysiology

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APA (6th Edition):

Chen, X. (2016). Regional disturbances by the [delta]F508 mutation on the cystic fibrosis transmembrane conductance regulator. (Doctoral Dissertation). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/238831

Chicago Manual of Style (16th Edition):

Chen, Xinying. “Regional disturbances by the [delta]F508 mutation on the cystic fibrosis transmembrane conductance regulator.” 2016. Doctoral Dissertation, University of Hong Kong. Accessed February 24, 2020. http://hdl.handle.net/10722/238831.

MLA Handbook (7th Edition):

Chen, Xinying. “Regional disturbances by the [delta]F508 mutation on the cystic fibrosis transmembrane conductance regulator.” 2016. Web. 24 Feb 2020.

Vancouver:

Chen X. Regional disturbances by the [delta]F508 mutation on the cystic fibrosis transmembrane conductance regulator. [Internet] [Doctoral dissertation]. University of Hong Kong; 2016. [cited 2020 Feb 24]. Available from: http://hdl.handle.net/10722/238831.

Council of Science Editors:

Chen X. Regional disturbances by the [delta]F508 mutation on the cystic fibrosis transmembrane conductance regulator. [Doctoral Dissertation]. University of Hong Kong; 2016. Available from: http://hdl.handle.net/10722/238831


University of Manchester

2. Wells, Emma Jane. THE ROLE OF PARENTING INTERVENTIONS IN PROMOTING TREATMENT ADHERENCE IN CYSTIC FIBROSIS.

Degree: 2016, University of Manchester

 Within the Cystic Fibrosis (CF) literature it is acknowledged that parents play a significant role in supporting children with treatment procedures. Furthermore, a number of… (more)

Subjects/Keywords: Cystic Fibrosis; Parenting

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APA (6th Edition):

Wells, E. J. (2016). THE ROLE OF PARENTING INTERVENTIONS IN PROMOTING TREATMENT ADHERENCE IN CYSTIC FIBROSIS. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:305054

Chicago Manual of Style (16th Edition):

Wells, Emma Jane. “THE ROLE OF PARENTING INTERVENTIONS IN PROMOTING TREATMENT ADHERENCE IN CYSTIC FIBROSIS.” 2016. Doctoral Dissertation, University of Manchester. Accessed February 24, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:305054.

MLA Handbook (7th Edition):

Wells, Emma Jane. “THE ROLE OF PARENTING INTERVENTIONS IN PROMOTING TREATMENT ADHERENCE IN CYSTIC FIBROSIS.” 2016. Web. 24 Feb 2020.

Vancouver:

Wells EJ. THE ROLE OF PARENTING INTERVENTIONS IN PROMOTING TREATMENT ADHERENCE IN CYSTIC FIBROSIS. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2020 Feb 24]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:305054.

Council of Science Editors:

Wells EJ. THE ROLE OF PARENTING INTERVENTIONS IN PROMOTING TREATMENT ADHERENCE IN CYSTIC FIBROSIS. [Doctoral Dissertation]. University of Manchester; 2016. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:305054


University of Manchester

3. Hughes, Guy. Electron tomography of mucins and their rôle in cystic fibrosis.

Degree: 2014, University of Manchester

 Although the primary defect in cystic fibrosis is the dysfunctional CFTR protein, the major pathology of the disease is due to aberrant mucus properties which… (more)

Subjects/Keywords: Cystic Fibrosis; Mucins

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APA (6th Edition):

Hughes, G. (2014). Electron tomography of mucins and their rôle in cystic fibrosis. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:225554

Chicago Manual of Style (16th Edition):

Hughes, Guy. “Electron tomography of mucins and their rôle in cystic fibrosis.” 2014. Doctoral Dissertation, University of Manchester. Accessed February 24, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:225554.

MLA Handbook (7th Edition):

Hughes, Guy. “Electron tomography of mucins and their rôle in cystic fibrosis.” 2014. Web. 24 Feb 2020.

Vancouver:

Hughes G. Electron tomography of mucins and their rôle in cystic fibrosis. [Internet] [Doctoral dissertation]. University of Manchester; 2014. [cited 2020 Feb 24]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:225554.

Council of Science Editors:

Hughes G. Electron tomography of mucins and their rôle in cystic fibrosis. [Doctoral Dissertation]. University of Manchester; 2014. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:225554


McMaster University

4. Nair, Gayatri. MOLECULAR AND CULTURE-BASED PROFILING OF SPUTUM MICROBIOTA FROM CYSTIC FIBROSIS PATIENTS.

Degree: MSc, 2019, McMaster University

Background/Objectives: Chronic airway infections, characterized by pulmonary exacerbations, are responsible for >90% of morbidity and mortality in CF. Although conventional CF pathogens are targets of… (more)

Subjects/Keywords: Cystic Fibrosis; Microbiology

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APA (6th Edition):

Nair, G. (2019). MOLECULAR AND CULTURE-BASED PROFILING OF SPUTUM MICROBIOTA FROM CYSTIC FIBROSIS PATIENTS. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/24974

Chicago Manual of Style (16th Edition):

Nair, Gayatri. “MOLECULAR AND CULTURE-BASED PROFILING OF SPUTUM MICROBIOTA FROM CYSTIC FIBROSIS PATIENTS.” 2019. Masters Thesis, McMaster University. Accessed February 24, 2020. http://hdl.handle.net/11375/24974.

MLA Handbook (7th Edition):

Nair, Gayatri. “MOLECULAR AND CULTURE-BASED PROFILING OF SPUTUM MICROBIOTA FROM CYSTIC FIBROSIS PATIENTS.” 2019. Web. 24 Feb 2020.

Vancouver:

Nair G. MOLECULAR AND CULTURE-BASED PROFILING OF SPUTUM MICROBIOTA FROM CYSTIC FIBROSIS PATIENTS. [Internet] [Masters thesis]. McMaster University; 2019. [cited 2020 Feb 24]. Available from: http://hdl.handle.net/11375/24974.

Council of Science Editors:

Nair G. MOLECULAR AND CULTURE-BASED PROFILING OF SPUTUM MICROBIOTA FROM CYSTIC FIBROSIS PATIENTS. [Masters Thesis]. McMaster University; 2019. Available from: http://hdl.handle.net/11375/24974


Hong Kong University of Science and Technology

5. Wang, Na. Regulation of CFTR by cytoskeletal protein vimentin.

Degree: 2012, Hong Kong University of Science and Technology

Cystic fibrosis transmembrane conductance regulator (CFTR) functions as an anion channel, conducting chloride and bicarbonate, and as a regulator of several membrane ion channels and… (more)

Subjects/Keywords: Cystic fibrosis ; Cytoskeleton

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APA (6th Edition):

Wang, N. (2012). Regulation of CFTR by cytoskeletal protein vimentin. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-73409 ; https://doi.org/10.14711/thesis-b1207883 ; http://repository.ust.hk/ir/bitstream/1783.1-73409/1/th_redirect.html

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Wang, Na. “Regulation of CFTR by cytoskeletal protein vimentin.” 2012. Thesis, Hong Kong University of Science and Technology. Accessed February 24, 2020. http://repository.ust.hk/ir/Record/1783.1-73409 ; https://doi.org/10.14711/thesis-b1207883 ; http://repository.ust.hk/ir/bitstream/1783.1-73409/1/th_redirect.html.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Wang, Na. “Regulation of CFTR by cytoskeletal protein vimentin.” 2012. Web. 24 Feb 2020.

Vancouver:

Wang N. Regulation of CFTR by cytoskeletal protein vimentin. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2012. [cited 2020 Feb 24]. Available from: http://repository.ust.hk/ir/Record/1783.1-73409 ; https://doi.org/10.14711/thesis-b1207883 ; http://repository.ust.hk/ir/bitstream/1783.1-73409/1/th_redirect.html.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Wang N. Regulation of CFTR by cytoskeletal protein vimentin. [Thesis]. Hong Kong University of Science and Technology; 2012. Available from: http://repository.ust.hk/ir/Record/1783.1-73409 ; https://doi.org/10.14711/thesis-b1207883 ; http://repository.ust.hk/ir/bitstream/1783.1-73409/1/th_redirect.html

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Alberta

6. Mohammad, Sohaib. From G551D to F508del: An Inquiry Into The Development Of Targeted Therapeutics For The Treatment Of Cystic Fibrosis.

Degree: MS, School of Public Health, 2016, University of Alberta

Cystic Fibrosis (CF) is a fatal inherited disease caused by mutations in the gene encoding the Cystic Fibrosis Transmembrane Regulator (CFTR) protein. CFTR plays an… (more)

Subjects/Keywords: Cystic Fibrosis; Kalydeco; Orkambi

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APA (6th Edition):

Mohammad, S. (2016). From G551D to F508del: An Inquiry Into The Development Of Targeted Therapeutics For The Treatment Of Cystic Fibrosis. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/crf55z790r

Chicago Manual of Style (16th Edition):

Mohammad, Sohaib. “From G551D to F508del: An Inquiry Into The Development Of Targeted Therapeutics For The Treatment Of Cystic Fibrosis.” 2016. Masters Thesis, University of Alberta. Accessed February 24, 2020. https://era.library.ualberta.ca/files/crf55z790r.

MLA Handbook (7th Edition):

Mohammad, Sohaib. “From G551D to F508del: An Inquiry Into The Development Of Targeted Therapeutics For The Treatment Of Cystic Fibrosis.” 2016. Web. 24 Feb 2020.

Vancouver:

Mohammad S. From G551D to F508del: An Inquiry Into The Development Of Targeted Therapeutics For The Treatment Of Cystic Fibrosis. [Internet] [Masters thesis]. University of Alberta; 2016. [cited 2020 Feb 24]. Available from: https://era.library.ualberta.ca/files/crf55z790r.

Council of Science Editors:

Mohammad S. From G551D to F508del: An Inquiry Into The Development Of Targeted Therapeutics For The Treatment Of Cystic Fibrosis. [Masters Thesis]. University of Alberta; 2016. Available from: https://era.library.ualberta.ca/files/crf55z790r


University of Alberta

7. Dasgupta, Bonnie. Novel approaches to mucolysis to improve mucus clearance in cystic fibrosis.

Degree: MS, Department of Medicine, 1995, University of Alberta

Subjects/Keywords: Cystic fibrosis.

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APA (6th Edition):

Dasgupta, B. (1995). Novel approaches to mucolysis to improve mucus clearance in cystic fibrosis. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/b5644t90p

Chicago Manual of Style (16th Edition):

Dasgupta, Bonnie. “Novel approaches to mucolysis to improve mucus clearance in cystic fibrosis.” 1995. Masters Thesis, University of Alberta. Accessed February 24, 2020. https://era.library.ualberta.ca/files/b5644t90p.

MLA Handbook (7th Edition):

Dasgupta, Bonnie. “Novel approaches to mucolysis to improve mucus clearance in cystic fibrosis.” 1995. Web. 24 Feb 2020.

Vancouver:

Dasgupta B. Novel approaches to mucolysis to improve mucus clearance in cystic fibrosis. [Internet] [Masters thesis]. University of Alberta; 1995. [cited 2020 Feb 24]. Available from: https://era.library.ualberta.ca/files/b5644t90p.

Council of Science Editors:

Dasgupta B. Novel approaches to mucolysis to improve mucus clearance in cystic fibrosis. [Masters Thesis]. University of Alberta; 1995. Available from: https://era.library.ualberta.ca/files/b5644t90p


University of Edinburgh

8. Jannetta, Evelyn Elena. Qualitative study of cystic fibrosis (CF) patients' expectations of gene therapy.

Degree: Thesis (D.Clin.Psy.), 2009, University of Edinburgh

 Introduction: Gene therapy is currently being developed for people with cystic fibrosis (CF), a life-threatening condition for which there is no cure. The UK CF… (more)

Subjects/Keywords: Cystic fibrosis; Gene therapy; Expectations

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APA (6th Edition):

Jannetta, E. E. (2009). Qualitative study of cystic fibrosis (CF) patients' expectations of gene therapy. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/8745

Chicago Manual of Style (16th Edition):

Jannetta, Evelyn Elena. “Qualitative study of cystic fibrosis (CF) patients' expectations of gene therapy.” 2009. Doctoral Dissertation, University of Edinburgh. Accessed February 24, 2020. http://hdl.handle.net/1842/8745.

MLA Handbook (7th Edition):

Jannetta, Evelyn Elena. “Qualitative study of cystic fibrosis (CF) patients' expectations of gene therapy.” 2009. Web. 24 Feb 2020.

Vancouver:

Jannetta EE. Qualitative study of cystic fibrosis (CF) patients' expectations of gene therapy. [Internet] [Doctoral dissertation]. University of Edinburgh; 2009. [cited 2020 Feb 24]. Available from: http://hdl.handle.net/1842/8745.

Council of Science Editors:

Jannetta EE. Qualitative study of cystic fibrosis (CF) patients' expectations of gene therapy. [Doctoral Dissertation]. University of Edinburgh; 2009. Available from: http://hdl.handle.net/1842/8745


Laurentian University

9. Alhariri, Moayad Abdulaziz I. Evaluation of liposomal bismuth-ethanedithiol-tobramycin for treatment of cystic fibrosis pulmonary pseudomonas aeruginosa infection .

Degree: 2013, Laurentian University

 The effectiveness of liposomes incorporating bismuth-ethanedithiol and loaded with tobramycin (LipoBiEDT-TOB) at sub-inhibitory concentrations to inhibit the production of quorum sensing signaling molecules and virulence… (more)

Subjects/Keywords: Cystic fibrosis; Liposomes; Aminoglycosides; Bacteria

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APA (6th Edition):

Alhariri, M. A. I. (2013). Evaluation of liposomal bismuth-ethanedithiol-tobramycin for treatment of cystic fibrosis pulmonary pseudomonas aeruginosa infection . (Thesis). Laurentian University. Retrieved from https://zone.biblio.laurentian.ca/dspace/handle/10219/2099

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Alhariri, Moayad Abdulaziz I. “Evaluation of liposomal bismuth-ethanedithiol-tobramycin for treatment of cystic fibrosis pulmonary pseudomonas aeruginosa infection .” 2013. Thesis, Laurentian University. Accessed February 24, 2020. https://zone.biblio.laurentian.ca/dspace/handle/10219/2099.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Alhariri, Moayad Abdulaziz I. “Evaluation of liposomal bismuth-ethanedithiol-tobramycin for treatment of cystic fibrosis pulmonary pseudomonas aeruginosa infection .” 2013. Web. 24 Feb 2020.

Vancouver:

Alhariri MAI. Evaluation of liposomal bismuth-ethanedithiol-tobramycin for treatment of cystic fibrosis pulmonary pseudomonas aeruginosa infection . [Internet] [Thesis]. Laurentian University; 2013. [cited 2020 Feb 24]. Available from: https://zone.biblio.laurentian.ca/dspace/handle/10219/2099.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Alhariri MAI. Evaluation of liposomal bismuth-ethanedithiol-tobramycin for treatment of cystic fibrosis pulmonary pseudomonas aeruginosa infection . [Thesis]. Laurentian University; 2013. Available from: https://zone.biblio.laurentian.ca/dspace/handle/10219/2099

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Louisville

10. Purdy, Megan E. Recovery and biogeography of Pseudomonas and Burkholderia species from the human home.

Degree: PhD, 2013, University of Louisville

 15 households in the Louisville Metro area were sampled, 7 had a patient with cystic fibrosis (CF), and 8 did not. Houses were sampled between… (more)

Subjects/Keywords: Biogeography; Pseudomonas; Burkholderia; Cystic Fibrosis

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APA (6th Edition):

Purdy, M. E. (2013). Recovery and biogeography of Pseudomonas and Burkholderia species from the human home. (Doctoral Dissertation). University of Louisville. Retrieved from 10.18297/etd/1166 ; https://ir.library.louisville.edu/etd/1166

Chicago Manual of Style (16th Edition):

Purdy, Megan E. “Recovery and biogeography of Pseudomonas and Burkholderia species from the human home.” 2013. Doctoral Dissertation, University of Louisville. Accessed February 24, 2020. 10.18297/etd/1166 ; https://ir.library.louisville.edu/etd/1166.

MLA Handbook (7th Edition):

Purdy, Megan E. “Recovery and biogeography of Pseudomonas and Burkholderia species from the human home.” 2013. Web. 24 Feb 2020.

Vancouver:

Purdy ME. Recovery and biogeography of Pseudomonas and Burkholderia species from the human home. [Internet] [Doctoral dissertation]. University of Louisville; 2013. [cited 2020 Feb 24]. Available from: 10.18297/etd/1166 ; https://ir.library.louisville.edu/etd/1166.

Council of Science Editors:

Purdy ME. Recovery and biogeography of Pseudomonas and Burkholderia species from the human home. [Doctoral Dissertation]. University of Louisville; 2013. Available from: 10.18297/etd/1166 ; https://ir.library.louisville.edu/etd/1166


Massey University

11. Doole, Pamela L. Getting on with life : the lived experience of four adults with cystic fibrosis.

Degree: M. Phil., Nursing, 1996, Massey University

Cystic fibrosis (CF) is a progressive, life limiting disease that requires relentless life long management. Although there are a small number of adults with CF… (more)

Subjects/Keywords: Cystic fibrosis

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APA (6th Edition):

Doole, P. L. (1996). Getting on with life : the lived experience of four adults with cystic fibrosis. (Masters Thesis). Massey University. Retrieved from http://hdl.handle.net/10179/6867

Chicago Manual of Style (16th Edition):

Doole, Pamela L. “Getting on with life : the lived experience of four adults with cystic fibrosis.” 1996. Masters Thesis, Massey University. Accessed February 24, 2020. http://hdl.handle.net/10179/6867.

MLA Handbook (7th Edition):

Doole, Pamela L. “Getting on with life : the lived experience of four adults with cystic fibrosis.” 1996. Web. 24 Feb 2020.

Vancouver:

Doole PL. Getting on with life : the lived experience of four adults with cystic fibrosis. [Internet] [Masters thesis]. Massey University; 1996. [cited 2020 Feb 24]. Available from: http://hdl.handle.net/10179/6867.

Council of Science Editors:

Doole PL. Getting on with life : the lived experience of four adults with cystic fibrosis. [Masters Thesis]. Massey University; 1996. Available from: http://hdl.handle.net/10179/6867


University of Manchester

12. Wells, Emma Jane. The role of parenting interventions in promoting treatment adherence in cystic fibrosis.

Degree: Thesis (D.Clin.Psy.), 2016, University of Manchester

 Within the Cystic Fibrosis (CF) literature it is acknowledged that parents play a significant role in supporting children with treatment procedures. Furthermore, a number of… (more)

Subjects/Keywords: 616.3; Cystic Fibrosis; Parenting

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APA (6th Edition):

Wells, E. J. (2016). The role of parenting interventions in promoting treatment adherence in cystic fibrosis. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/the-role-of-parenting-interventions-in-promoting-treatment-adherence-in-cystic-fibrosis(bc291fe1-393b-43a3-9749-3165e4372539).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.697765

Chicago Manual of Style (16th Edition):

Wells, Emma Jane. “The role of parenting interventions in promoting treatment adherence in cystic fibrosis.” 2016. Doctoral Dissertation, University of Manchester. Accessed February 24, 2020. https://www.research.manchester.ac.uk/portal/en/theses/the-role-of-parenting-interventions-in-promoting-treatment-adherence-in-cystic-fibrosis(bc291fe1-393b-43a3-9749-3165e4372539).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.697765.

MLA Handbook (7th Edition):

Wells, Emma Jane. “The role of parenting interventions in promoting treatment adherence in cystic fibrosis.” 2016. Web. 24 Feb 2020.

Vancouver:

Wells EJ. The role of parenting interventions in promoting treatment adherence in cystic fibrosis. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2020 Feb 24]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/the-role-of-parenting-interventions-in-promoting-treatment-adherence-in-cystic-fibrosis(bc291fe1-393b-43a3-9749-3165e4372539).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.697765.

Council of Science Editors:

Wells EJ. The role of parenting interventions in promoting treatment adherence in cystic fibrosis. [Doctoral Dissertation]. University of Manchester; 2016. Available from: https://www.research.manchester.ac.uk/portal/en/theses/the-role-of-parenting-interventions-in-promoting-treatment-adherence-in-cystic-fibrosis(bc291fe1-393b-43a3-9749-3165e4372539).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.697765


University of Cambridge

13. Rodriguez Rincon, Daniela. Tackling Mycobacterium abscessus infection in Cystic Fibrosis.

Degree: PhD, 2018, University of Cambridge

 Mycobacterium abscessus is an emerging pathogen with infections increasing worldwide, especially among Cystic Fibrosis (CF) patients. During my PhD, I studied key aspects of the… (more)

Subjects/Keywords: Mycobacterium; abscessus; infection; cystic; fibrosis

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APA (6th Edition):

Rodriguez Rincon, D. (2018). Tackling Mycobacterium abscessus infection in Cystic Fibrosis. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/275473

Chicago Manual of Style (16th Edition):

Rodriguez Rincon, Daniela. “Tackling Mycobacterium abscessus infection in Cystic Fibrosis.” 2018. Doctoral Dissertation, University of Cambridge. Accessed February 24, 2020. https://www.repository.cam.ac.uk/handle/1810/275473.

MLA Handbook (7th Edition):

Rodriguez Rincon, Daniela. “Tackling Mycobacterium abscessus infection in Cystic Fibrosis.” 2018. Web. 24 Feb 2020.

Vancouver:

Rodriguez Rincon D. Tackling Mycobacterium abscessus infection in Cystic Fibrosis. [Internet] [Doctoral dissertation]. University of Cambridge; 2018. [cited 2020 Feb 24]. Available from: https://www.repository.cam.ac.uk/handle/1810/275473.

Council of Science Editors:

Rodriguez Rincon D. Tackling Mycobacterium abscessus infection in Cystic Fibrosis. [Doctoral Dissertation]. University of Cambridge; 2018. Available from: https://www.repository.cam.ac.uk/handle/1810/275473


Universitat Rovira i Virgili

14. Nasef, Hany Abdel Hady Abdel Rahman. Temperature modulated genosensor for detection of cystic fibrosis mutations.

Degree: Departament d'Enginyeria Química, 2010, Universitat Rovira i Virgili

 La memoria de la tesis está organizada en 8 capítulos. Un resumen de cada capítulo se detalla a continuación. El Capítulo 1 es una Introducción,… (more)

Subjects/Keywords: Cystic fibrosis; DF508; genosensor; 543

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APA (6th Edition):

Nasef, H. A. H. A. R. (2010). Temperature modulated genosensor for detection of cystic fibrosis mutations. (Thesis). Universitat Rovira i Virgili. Retrieved from http://hdl.handle.net/10803/8585

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Nasef, Hany Abdel Hady Abdel Rahman. “Temperature modulated genosensor for detection of cystic fibrosis mutations.” 2010. Thesis, Universitat Rovira i Virgili. Accessed February 24, 2020. http://hdl.handle.net/10803/8585.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Nasef, Hany Abdel Hady Abdel Rahman. “Temperature modulated genosensor for detection of cystic fibrosis mutations.” 2010. Web. 24 Feb 2020.

Vancouver:

Nasef HAHAR. Temperature modulated genosensor for detection of cystic fibrosis mutations. [Internet] [Thesis]. Universitat Rovira i Virgili; 2010. [cited 2020 Feb 24]. Available from: http://hdl.handle.net/10803/8585.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Nasef HAHAR. Temperature modulated genosensor for detection of cystic fibrosis mutations. [Thesis]. Universitat Rovira i Virgili; 2010. Available from: http://hdl.handle.net/10803/8585

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Toronto

15. Ghorbani, Peyman. Short-chain Fatty Acids Modulate Bacterial Growth and Airway Epithelial Cell Inflammatory Responses.

Degree: 2012, University of Toronto

Short-chain fatty acids (SCFAs) are anaerobic bacterial metabolites. Cystic fibrosis (CF) lung disease is a condition caused by mutations in the cystic fibrosis transmembrane conductange… (more)

Subjects/Keywords: cystic fibrosis; inflammation; 0306; 0719

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APA (6th Edition):

Ghorbani, P. (2012). Short-chain Fatty Acids Modulate Bacterial Growth and Airway Epithelial Cell Inflammatory Responses. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/33204

Chicago Manual of Style (16th Edition):

Ghorbani, Peyman. “Short-chain Fatty Acids Modulate Bacterial Growth and Airway Epithelial Cell Inflammatory Responses.” 2012. Masters Thesis, University of Toronto. Accessed February 24, 2020. http://hdl.handle.net/1807/33204.

MLA Handbook (7th Edition):

Ghorbani, Peyman. “Short-chain Fatty Acids Modulate Bacterial Growth and Airway Epithelial Cell Inflammatory Responses.” 2012. Web. 24 Feb 2020.

Vancouver:

Ghorbani P. Short-chain Fatty Acids Modulate Bacterial Growth and Airway Epithelial Cell Inflammatory Responses. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2020 Feb 24]. Available from: http://hdl.handle.net/1807/33204.

Council of Science Editors:

Ghorbani P. Short-chain Fatty Acids Modulate Bacterial Growth and Airway Epithelial Cell Inflammatory Responses. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/33204


University of Toronto

16. Ghorbani, Peyman. Short-chain Fatty Acids Modulate Bacterial Growth and Airway Epithelial Cell Inflammatory Responses.

Degree: 2012, University of Toronto

Short-chain fatty acids (SCFAs) are anaerobic bacterial metabolites. Cystic fibrosis (CF) lung disease is a condition caused by mutations in the cystic fibrosis transmembrane conductange… (more)

Subjects/Keywords: cystic fibrosis; inflammation; 0306

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APA (6th Edition):

Ghorbani, P. (2012). Short-chain Fatty Acids Modulate Bacterial Growth and Airway Epithelial Cell Inflammatory Responses. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/33203

Chicago Manual of Style (16th Edition):

Ghorbani, Peyman. “Short-chain Fatty Acids Modulate Bacterial Growth and Airway Epithelial Cell Inflammatory Responses.” 2012. Masters Thesis, University of Toronto. Accessed February 24, 2020. http://hdl.handle.net/1807/33203.

MLA Handbook (7th Edition):

Ghorbani, Peyman. “Short-chain Fatty Acids Modulate Bacterial Growth and Airway Epithelial Cell Inflammatory Responses.” 2012. Web. 24 Feb 2020.

Vancouver:

Ghorbani P. Short-chain Fatty Acids Modulate Bacterial Growth and Airway Epithelial Cell Inflammatory Responses. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2020 Feb 24]. Available from: http://hdl.handle.net/1807/33203.

Council of Science Editors:

Ghorbani P. Short-chain Fatty Acids Modulate Bacterial Growth and Airway Epithelial Cell Inflammatory Responses. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/33203


University of Adelaide

17. Kremer, Karlea Lee. Cystic Fibrosis gene therapy: methods for the optimisation of CFTR gene delivery.

Degree: 2010, University of Adelaide

 Gene therapy potentially holds the key for the treatment and cure of many genetic diseases, including cystic fibrosis. A number of delivery methods have been… (more)

Subjects/Keywords: cystic fibrosis; gene therapy; lentivirus

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Kremer, K. L. (2010). Cystic Fibrosis gene therapy: methods for the optimisation of CFTR gene delivery. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/63153

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Kremer, Karlea Lee. “Cystic Fibrosis gene therapy: methods for the optimisation of CFTR gene delivery.” 2010. Thesis, University of Adelaide. Accessed February 24, 2020. http://hdl.handle.net/2440/63153.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Kremer, Karlea Lee. “Cystic Fibrosis gene therapy: methods for the optimisation of CFTR gene delivery.” 2010. Web. 24 Feb 2020.

Vancouver:

Kremer KL. Cystic Fibrosis gene therapy: methods for the optimisation of CFTR gene delivery. [Internet] [Thesis]. University of Adelaide; 2010. [cited 2020 Feb 24]. Available from: http://hdl.handle.net/2440/63153.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Kremer KL. Cystic Fibrosis gene therapy: methods for the optimisation of CFTR gene delivery. [Thesis]. University of Adelaide; 2010. Available from: http://hdl.handle.net/2440/63153

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Toronto

18. Hung, Maurita. The Development and Characterization of VX-770 Molecular Probes.

Degree: 2016, University of Toronto

Cystic fibrosis is the most common genetic disease affecting the Canadian population. It is caused by mutations in the cystic fibrosis transmembrane conductance regulator gene,… (more)

Subjects/Keywords: CFTR; cystic fibrosis; potentiator; 0719

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APA (6th Edition):

Hung, M. (2016). The Development and Characterization of VX-770 Molecular Probes. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/89009

Chicago Manual of Style (16th Edition):

Hung, Maurita. “The Development and Characterization of VX-770 Molecular Probes.” 2016. Masters Thesis, University of Toronto. Accessed February 24, 2020. http://hdl.handle.net/1807/89009.

MLA Handbook (7th Edition):

Hung, Maurita. “The Development and Characterization of VX-770 Molecular Probes.” 2016. Web. 24 Feb 2020.

Vancouver:

Hung M. The Development and Characterization of VX-770 Molecular Probes. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2020 Feb 24]. Available from: http://hdl.handle.net/1807/89009.

Council of Science Editors:

Hung M. The Development and Characterization of VX-770 Molecular Probes. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/89009


Rutgers University

19. Dekerlegand, Robert, 1970-. Inspiratory muscle strength in adults with stable cystic fibrosis: clinical predictors and the influence of disease severity.

Degree: PhD, Health Sciences, 2014, Rutgers University

Introduction: The work of breathing (WOB) imposed on the inspiratory muscles (IM) is elevated in cystic fibrosis (CF). Impaired inspiratory muscle strength (IMS) may contribute… (more)

Subjects/Keywords: Cystic fibrosis – Patients; Muscle strength

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APA (6th Edition):

Dekerlegand, Robert, 1. (2014). Inspiratory muscle strength in adults with stable cystic fibrosis: clinical predictors and the influence of disease severity. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/45638/

Chicago Manual of Style (16th Edition):

Dekerlegand, Robert, 1970-. “Inspiratory muscle strength in adults with stable cystic fibrosis: clinical predictors and the influence of disease severity.” 2014. Doctoral Dissertation, Rutgers University. Accessed February 24, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/45638/.

MLA Handbook (7th Edition):

Dekerlegand, Robert, 1970-. “Inspiratory muscle strength in adults with stable cystic fibrosis: clinical predictors and the influence of disease severity.” 2014. Web. 24 Feb 2020.

Vancouver:

Dekerlegand, Robert 1. Inspiratory muscle strength in adults with stable cystic fibrosis: clinical predictors and the influence of disease severity. [Internet] [Doctoral dissertation]. Rutgers University; 2014. [cited 2020 Feb 24]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/45638/.

Council of Science Editors:

Dekerlegand, Robert 1. Inspiratory muscle strength in adults with stable cystic fibrosis: clinical predictors and the influence of disease severity. [Doctoral Dissertation]. Rutgers University; 2014. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/45638/


Rutgers University

20. Kbah, Noor, 1987-. Nanotechnology approach for treatment of cystic fibrosis.

Degree: MS, Pharmaceutical Science, 2016, Rutgers University

Cystic fibrosis is a lethal, hereditary disease, caused by mutations in the gene cystic fibrosis transmembrane conductance regulator (CFTR) where it affects a cAMP-activated chloride… (more)

Subjects/Keywords: Nanotechnology; Cystic fibrosis – Treatment

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APA (6th Edition):

Kbah, Noor, 1. (2016). Nanotechnology approach for treatment of cystic fibrosis. (Masters Thesis). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/49245/

Chicago Manual of Style (16th Edition):

Kbah, Noor, 1987-. “Nanotechnology approach for treatment of cystic fibrosis.” 2016. Masters Thesis, Rutgers University. Accessed February 24, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/49245/.

MLA Handbook (7th Edition):

Kbah, Noor, 1987-. “Nanotechnology approach for treatment of cystic fibrosis.” 2016. Web. 24 Feb 2020.

Vancouver:

Kbah, Noor 1. Nanotechnology approach for treatment of cystic fibrosis. [Internet] [Masters thesis]. Rutgers University; 2016. [cited 2020 Feb 24]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/49245/.

Council of Science Editors:

Kbah, Noor 1. Nanotechnology approach for treatment of cystic fibrosis. [Masters Thesis]. Rutgers University; 2016. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/49245/


Laurentian University

21. Alhariri, Moayad Abdulaziz I. Evaluation of liposomal bismuth-ethanedithiol-tobramycin for treatment of cystic fibrosis pulmonary pseudomonas aeruginosa infection .

Degree: 2013, Laurentian University

 The effectiveness of liposomes incorporating bismuth-ethanedithiol and loaded with tobramycin (LipoBiEDT-TOB) at sub-inhibitory concentrations to inhibit the production of quorum sensing signaling molecules and virulence… (more)

Subjects/Keywords: Cystic fibrosis; Liposomes; Aminoglycosides; Bacteria

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APA (6th Edition):

Alhariri, M. A. I. (2013). Evaluation of liposomal bismuth-ethanedithiol-tobramycin for treatment of cystic fibrosis pulmonary pseudomonas aeruginosa infection . (Thesis). Laurentian University. Retrieved from https://zone.biblio.laurentian.ca/dspace/handle/10219/2099

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Alhariri, Moayad Abdulaziz I. “Evaluation of liposomal bismuth-ethanedithiol-tobramycin for treatment of cystic fibrosis pulmonary pseudomonas aeruginosa infection .” 2013. Thesis, Laurentian University. Accessed February 24, 2020. https://zone.biblio.laurentian.ca/dspace/handle/10219/2099.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Alhariri, Moayad Abdulaziz I. “Evaluation of liposomal bismuth-ethanedithiol-tobramycin for treatment of cystic fibrosis pulmonary pseudomonas aeruginosa infection .” 2013. Web. 24 Feb 2020.

Vancouver:

Alhariri MAI. Evaluation of liposomal bismuth-ethanedithiol-tobramycin for treatment of cystic fibrosis pulmonary pseudomonas aeruginosa infection . [Internet] [Thesis]. Laurentian University; 2013. [cited 2020 Feb 24]. Available from: https://zone.biblio.laurentian.ca/dspace/handle/10219/2099.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Alhariri MAI. Evaluation of liposomal bismuth-ethanedithiol-tobramycin for treatment of cystic fibrosis pulmonary pseudomonas aeruginosa infection . [Thesis]. Laurentian University; 2013. Available from: https://zone.biblio.laurentian.ca/dspace/handle/10219/2099

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Limerick

22. Quigley, Stephen James. Knowledge is wealth: investigating psychosocial distress and ameliorating knowledge deficiencies in parents of children identified, through newborn screening in Ireland, as carrying an altered cystic fibrosis gene.

Degree: 2014, University of Limerick

Cystic Fibrosis is an inherited disease affecting mainly the lungs and digestive system. In Ireland, the incidence of cystic fibrosis is 1 in 1,461 births,… (more)

Subjects/Keywords: cystic fibrosis; CF; genetic testing

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APA (6th Edition):

Quigley, S. J. (2014). Knowledge is wealth: investigating psychosocial distress and ameliorating knowledge deficiencies in parents of children identified, through newborn screening in Ireland, as carrying an altered cystic fibrosis gene. (Thesis). University of Limerick. Retrieved from http://hdl.handle.net/10344/4318

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Quigley, Stephen James. “Knowledge is wealth: investigating psychosocial distress and ameliorating knowledge deficiencies in parents of children identified, through newborn screening in Ireland, as carrying an altered cystic fibrosis gene.” 2014. Thesis, University of Limerick. Accessed February 24, 2020. http://hdl.handle.net/10344/4318.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Quigley, Stephen James. “Knowledge is wealth: investigating psychosocial distress and ameliorating knowledge deficiencies in parents of children identified, through newborn screening in Ireland, as carrying an altered cystic fibrosis gene.” 2014. Web. 24 Feb 2020.

Vancouver:

Quigley SJ. Knowledge is wealth: investigating psychosocial distress and ameliorating knowledge deficiencies in parents of children identified, through newborn screening in Ireland, as carrying an altered cystic fibrosis gene. [Internet] [Thesis]. University of Limerick; 2014. [cited 2020 Feb 24]. Available from: http://hdl.handle.net/10344/4318.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Quigley SJ. Knowledge is wealth: investigating psychosocial distress and ameliorating knowledge deficiencies in parents of children identified, through newborn screening in Ireland, as carrying an altered cystic fibrosis gene. [Thesis]. University of Limerick; 2014. Available from: http://hdl.handle.net/10344/4318

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Washington

23. Ramos, Kathleen Jessica. Heterogeneity in survival among adult cystic fibrosis patients with low lung function in the United States.

Degree: 2017, University of Washington

 Background Lung transplantation (LTx) is frequently considered for patients with cystic fibrosis (CF) when FEV1 reaches <30%. This study estimated transplant-free survival for patients with… (more)

Subjects/Keywords: cystic fibrosis; survival; Medicine; epidemiology

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APA (6th Edition):

Ramos, K. J. (2017). Heterogeneity in survival among adult cystic fibrosis patients with low lung function in the United States. (Thesis). University of Washington. Retrieved from http://hdl.handle.net/1773/38129

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Ramos, Kathleen Jessica. “Heterogeneity in survival among adult cystic fibrosis patients with low lung function in the United States.” 2017. Thesis, University of Washington. Accessed February 24, 2020. http://hdl.handle.net/1773/38129.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Ramos, Kathleen Jessica. “Heterogeneity in survival among adult cystic fibrosis patients with low lung function in the United States.” 2017. Web. 24 Feb 2020.

Vancouver:

Ramos KJ. Heterogeneity in survival among adult cystic fibrosis patients with low lung function in the United States. [Internet] [Thesis]. University of Washington; 2017. [cited 2020 Feb 24]. Available from: http://hdl.handle.net/1773/38129.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Ramos KJ. Heterogeneity in survival among adult cystic fibrosis patients with low lung function in the United States. [Thesis]. University of Washington; 2017. Available from: http://hdl.handle.net/1773/38129

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

24. LIDDY, ANNE MARIE. The Pharmacokinetic Interaction between Ivacaftor and Ritonavir.

Degree: School of Medicine. Discipline of Pharmacology & Therapeutics, 2019, Trinity College Dublin

 Ivacaftor is the first small molecule for the treatment of cystic fibrosis (CF) that directly targets the inherited defect in the cystic fibrosis transmembrane conductance… (more)

Subjects/Keywords: Ivacaftor; Cystic fibrosis; Pharmacokinetics

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APA (6th Edition):

LIDDY, A. M. (2019). The Pharmacokinetic Interaction between Ivacaftor and Ritonavir. (Thesis). Trinity College Dublin. Retrieved from http://hdl.handle.net/2262/85718

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

LIDDY, ANNE MARIE. “The Pharmacokinetic Interaction between Ivacaftor and Ritonavir.” 2019. Thesis, Trinity College Dublin. Accessed February 24, 2020. http://hdl.handle.net/2262/85718.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

LIDDY, ANNE MARIE. “The Pharmacokinetic Interaction between Ivacaftor and Ritonavir.” 2019. Web. 24 Feb 2020.

Vancouver:

LIDDY AM. The Pharmacokinetic Interaction between Ivacaftor and Ritonavir. [Internet] [Thesis]. Trinity College Dublin; 2019. [cited 2020 Feb 24]. Available from: http://hdl.handle.net/2262/85718.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

LIDDY AM. The Pharmacokinetic Interaction between Ivacaftor and Ritonavir. [Thesis]. Trinity College Dublin; 2019. Available from: http://hdl.handle.net/2262/85718

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Michigan State University

25. Nickerson, John Munro. Cellular and biochemical aspects of cystic fibrosis.

Degree: MS, 1976, Michigan State University

Subjects/Keywords: Cystic fibrosis

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APA (6th Edition):

Nickerson, J. M. (1976). Cellular and biochemical aspects of cystic fibrosis. (Masters Thesis). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:12536

Chicago Manual of Style (16th Edition):

Nickerson, John Munro. “Cellular and biochemical aspects of cystic fibrosis.” 1976. Masters Thesis, Michigan State University. Accessed February 24, 2020. http://etd.lib.msu.edu/islandora/object/etd:12536.

MLA Handbook (7th Edition):

Nickerson, John Munro. “Cellular and biochemical aspects of cystic fibrosis.” 1976. Web. 24 Feb 2020.

Vancouver:

Nickerson JM. Cellular and biochemical aspects of cystic fibrosis. [Internet] [Masters thesis]. Michigan State University; 1976. [cited 2020 Feb 24]. Available from: http://etd.lib.msu.edu/islandora/object/etd:12536.

Council of Science Editors:

Nickerson JM. Cellular and biochemical aspects of cystic fibrosis. [Masters Thesis]. Michigan State University; 1976. Available from: http://etd.lib.msu.edu/islandora/object/etd:12536

26. Bronsveld, Inez. Modifying Factors of Cystic Fibrosis Disease: Residual Chloride Secrefion, Genefic Background and Epigenetics.

Degree: Department of Pediatrics, 2000, Erasmus University Medical Center

 textabstractCystic fibrosis (CF) is an autosomal recessive disease caused by genetic lesions in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. This CFTR gene was… (more)

Subjects/Keywords: cystic fibrosis

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APA (6th Edition):

Bronsveld, I. (2000). Modifying Factors of Cystic Fibrosis Disease: Residual Chloride Secrefion, Genefic Background and Epigenetics. (Doctoral Dissertation). Erasmus University Medical Center. Retrieved from http://hdl.handle.net/1765/16763

Chicago Manual of Style (16th Edition):

Bronsveld, Inez. “Modifying Factors of Cystic Fibrosis Disease: Residual Chloride Secrefion, Genefic Background and Epigenetics.” 2000. Doctoral Dissertation, Erasmus University Medical Center. Accessed February 24, 2020. http://hdl.handle.net/1765/16763.

MLA Handbook (7th Edition):

Bronsveld, Inez. “Modifying Factors of Cystic Fibrosis Disease: Residual Chloride Secrefion, Genefic Background and Epigenetics.” 2000. Web. 24 Feb 2020.

Vancouver:

Bronsveld I. Modifying Factors of Cystic Fibrosis Disease: Residual Chloride Secrefion, Genefic Background and Epigenetics. [Internet] [Doctoral dissertation]. Erasmus University Medical Center; 2000. [cited 2020 Feb 24]. Available from: http://hdl.handle.net/1765/16763.

Council of Science Editors:

Bronsveld I. Modifying Factors of Cystic Fibrosis Disease: Residual Chloride Secrefion, Genefic Background and Epigenetics. [Doctoral Dissertation]. Erasmus University Medical Center; 2000. Available from: http://hdl.handle.net/1765/16763


University of Minnesota

27. Apostolidou, Ioanna. Risk of introperative hypotension in cystiv fibrosis patients with and without diabetes: a pilot study.

Degree: MS, Clinical research, 2012, University of Minnesota

University of Minnesota M.S. thesis. December 2012. Major: Clinical research. Advisor: Antoinette Moran, MD. 1 computer file (pDF); vi, 21 pages.

Objective: In this pilot… (more)

Subjects/Keywords: Cardiac autonomic neuropathy; Cystic fibrosis; Cystic fibrosis-related diabetes; Intraoperative hypotension

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APA (6th Edition):

Apostolidou, I. (2012). Risk of introperative hypotension in cystiv fibrosis patients with and without diabetes: a pilot study. (Masters Thesis). University of Minnesota. Retrieved from http://purl.umn.edu/143929

Chicago Manual of Style (16th Edition):

Apostolidou, Ioanna. “Risk of introperative hypotension in cystiv fibrosis patients with and without diabetes: a pilot study.” 2012. Masters Thesis, University of Minnesota. Accessed February 24, 2020. http://purl.umn.edu/143929.

MLA Handbook (7th Edition):

Apostolidou, Ioanna. “Risk of introperative hypotension in cystiv fibrosis patients with and without diabetes: a pilot study.” 2012. Web. 24 Feb 2020.

Vancouver:

Apostolidou I. Risk of introperative hypotension in cystiv fibrosis patients with and without diabetes: a pilot study. [Internet] [Masters thesis]. University of Minnesota; 2012. [cited 2020 Feb 24]. Available from: http://purl.umn.edu/143929.

Council of Science Editors:

Apostolidou I. Risk of introperative hypotension in cystiv fibrosis patients with and without diabetes: a pilot study. [Masters Thesis]. University of Minnesota; 2012. Available from: http://purl.umn.edu/143929


University of Minnesota

28. Apostolidou, Ioanna. Risk of introperative hypotension in cystiv fibrosis patients with and without diabetes: a pilot study.

Degree: MS, Clinical research, 2012, University of Minnesota

 Objective: In this pilot study, we evaluated the incidence and severity of intraoperative hypotension and its relationship to CAN in patients with CFRD. We compared… (more)

Subjects/Keywords: Cardiac autonomic neuropathy; Cystic fibrosis; Cystic fibrosis-related diabetes; Intraoperative hypotension

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APA (6th Edition):

Apostolidou, I. (2012). Risk of introperative hypotension in cystiv fibrosis patients with and without diabetes: a pilot study. (Masters Thesis). University of Minnesota. Retrieved from http://purl.umn.edu/143929

Chicago Manual of Style (16th Edition):

Apostolidou, Ioanna. “Risk of introperative hypotension in cystiv fibrosis patients with and without diabetes: a pilot study.” 2012. Masters Thesis, University of Minnesota. Accessed February 24, 2020. http://purl.umn.edu/143929.

MLA Handbook (7th Edition):

Apostolidou, Ioanna. “Risk of introperative hypotension in cystiv fibrosis patients with and without diabetes: a pilot study.” 2012. Web. 24 Feb 2020.

Vancouver:

Apostolidou I. Risk of introperative hypotension in cystiv fibrosis patients with and without diabetes: a pilot study. [Internet] [Masters thesis]. University of Minnesota; 2012. [cited 2020 Feb 24]. Available from: http://purl.umn.edu/143929.

Council of Science Editors:

Apostolidou I. Risk of introperative hypotension in cystiv fibrosis patients with and without diabetes: a pilot study. [Masters Thesis]. University of Minnesota; 2012. Available from: http://purl.umn.edu/143929


University of Illinois – Urbana-Champaign

29. Sellers, Zachary M. Defining a role for the cystic fibrosis transmembrane conductance regulator in the heart.

Degree: PhD, 0325, 2010, University of Illinois – Urbana-Champaign

 While cystic fibrosis (CF) is commonly thought of as a lung disease, since it???s first description 70 years ago we have come to understand that… (more)

Subjects/Keywords: cystic fibrosis; Cystic fibrosis transmembrane conductance regulator (CFTR); cardiac myocyte; heart

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APA (6th Edition):

Sellers, Z. M. (2010). Defining a role for the cystic fibrosis transmembrane conductance regulator in the heart. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/15519

Chicago Manual of Style (16th Edition):

Sellers, Zachary M. “Defining a role for the cystic fibrosis transmembrane conductance regulator in the heart.” 2010. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed February 24, 2020. http://hdl.handle.net/2142/15519.

MLA Handbook (7th Edition):

Sellers, Zachary M. “Defining a role for the cystic fibrosis transmembrane conductance regulator in the heart.” 2010. Web. 24 Feb 2020.

Vancouver:

Sellers ZM. Defining a role for the cystic fibrosis transmembrane conductance regulator in the heart. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2010. [cited 2020 Feb 24]. Available from: http://hdl.handle.net/2142/15519.

Council of Science Editors:

Sellers ZM. Defining a role for the cystic fibrosis transmembrane conductance regulator in the heart. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2010. Available from: http://hdl.handle.net/2142/15519


Ryerson University

30. Elmallah, Salma. Progress Toward The Synthesis Of Labeled Derivatives Of The Cystic Fibrosis Drug Ivacaftor.

Degree: 2012, Ryerson University

Cystic fibrosis (CF) is one of the most common genetic diseases, affecting approximately 70,000 people worldwide causing severe complications and often leading to early death.… (more)

Subjects/Keywords: Cystic fibrosis  – Pathophysiology; Cystic fibrosis  – Treatment; Drugs  – Design; Pharmaceutical chemistry

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APA (6th Edition):

Elmallah, S. (2012). Progress Toward The Synthesis Of Labeled Derivatives Of The Cystic Fibrosis Drug Ivacaftor. (Thesis). Ryerson University. Retrieved from https://digital.library.ryerson.ca/islandora/object/RULA%3A1478

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Elmallah, Salma. “Progress Toward The Synthesis Of Labeled Derivatives Of The Cystic Fibrosis Drug Ivacaftor.” 2012. Thesis, Ryerson University. Accessed February 24, 2020. https://digital.library.ryerson.ca/islandora/object/RULA%3A1478.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Elmallah, Salma. “Progress Toward The Synthesis Of Labeled Derivatives Of The Cystic Fibrosis Drug Ivacaftor.” 2012. Web. 24 Feb 2020.

Vancouver:

Elmallah S. Progress Toward The Synthesis Of Labeled Derivatives Of The Cystic Fibrosis Drug Ivacaftor. [Internet] [Thesis]. Ryerson University; 2012. [cited 2020 Feb 24]. Available from: https://digital.library.ryerson.ca/islandora/object/RULA%3A1478.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Elmallah S. Progress Toward The Synthesis Of Labeled Derivatives Of The Cystic Fibrosis Drug Ivacaftor. [Thesis]. Ryerson University; 2012. Available from: https://digital.library.ryerson.ca/islandora/object/RULA%3A1478

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

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