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You searched for subject:(cystic fibrosis). Showing records 1 – 30 of 930 total matches.

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University of Manchester

1. 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 April 16, 2021. 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. 16 Apr 2021.

Vancouver:

Wells EJ. THE ROLE OF PARENTING INTERVENTIONS IN PROMOTING TREATMENT ADHERENCE IN CYSTIC FIBROSIS. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2021 Apr 16]. 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


McMaster University

2. 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 April 16, 2021. 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. 16 Apr 2021.

Vancouver:

Nair G. MOLECULAR AND CULTURE-BASED PROFILING OF SPUTUM MICROBIOTA FROM CYSTIC FIBROSIS PATIENTS. [Internet] [Masters thesis]. McMaster University; 2019. [cited 2021 Apr 16]. 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


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 April 16, 2021. 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. 16 Apr 2021.

Vancouver:

Hughes G. Electron tomography of mucins and their rôle in cystic fibrosis. [Internet] [Doctoral dissertation]. University of Manchester; 2014. [cited 2021 Apr 16]. 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


Hong Kong University of Science and Technology

4. 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 April 16, 2021. 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. 16 Apr 2021.

Vancouver:

Wang N. Regulation of CFTR by cytoskeletal protein vimentin. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2012. [cited 2021 Apr 16]. 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 Saskatchewan

5. Givzad, Naseem. Abnormal electrophysiological properties in sensory neurons from a swine model of cystic fibrosis.

Degree: 2020, University of Saskatchewan

Cystic fibrosis (CF) results from dysfunction of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) protein. CF has traditionally been considered a pediatric disease, but the… (more)

Subjects/Keywords: cystic fibrosis; neuropathy

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APA (6th Edition):

Givzad, N. (2020). Abnormal electrophysiological properties in sensory neurons from a swine model of cystic fibrosis. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/13009

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):

Givzad, Naseem. “Abnormal electrophysiological properties in sensory neurons from a swine model of cystic fibrosis.” 2020. Thesis, University of Saskatchewan. Accessed April 16, 2021. http://hdl.handle.net/10388/13009.

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

MLA Handbook (7th Edition):

Givzad, Naseem. “Abnormal electrophysiological properties in sensory neurons from a swine model of cystic fibrosis.” 2020. Web. 16 Apr 2021.

Vancouver:

Givzad N. Abnormal electrophysiological properties in sensory neurons from a swine model of cystic fibrosis. [Internet] [Thesis]. University of Saskatchewan; 2020. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/10388/13009.

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

Council of Science Editors:

Givzad N. Abnormal electrophysiological properties in sensory neurons from a swine model of cystic fibrosis. [Thesis]. University of Saskatchewan; 2020. Available from: http://hdl.handle.net/10388/13009

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 April 16, 2021. 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. 16 Apr 2021.

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 2021 Apr 16]. 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 April 16, 2021. 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. 16 Apr 2021.

Vancouver:

Dasgupta B. Novel approaches to mucolysis to improve mucus clearance in cystic fibrosis. [Internet] [Masters thesis]. University of Alberta; 1995. [cited 2021 Apr 16]. 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 Toronto

8. 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 April 16, 2021. 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. 16 Apr 2021.

Vancouver:

Ghorbani P. Short-chain Fatty Acids Modulate Bacterial Growth and Airway Epithelial Cell Inflammatory Responses. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2021 Apr 16]. 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

9. 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 April 16, 2021. 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. 16 Apr 2021.

Vancouver:

Ghorbani P. Short-chain Fatty Acids Modulate Bacterial Growth and Airway Epithelial Cell Inflammatory Responses. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2021 Apr 16]. 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


Virginia Commonwealth University

10. Borschuk, Adrienne P. Scoring and Validation of the Cystic Fibrosis Disclosure Questionnaire.

Degree: PhD, Psychology, 2015, Virginia Commonwealth University

  As more patients with cystic fibrosis (CF) are living into adulthood, patients may need to disclose their CF status to others, such as in… (more)

Subjects/Keywords: cystic fibrosis; disclosure; validation; psychometrics

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APA (6th Edition):

Borschuk, A. P. (2015). Scoring and Validation of the Cystic Fibrosis Disclosure Questionnaire. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://doi.org/10.25772/K3QW-K181 ; https://scholarscompass.vcu.edu/etd/4318

Chicago Manual of Style (16th Edition):

Borschuk, Adrienne P. “Scoring and Validation of the Cystic Fibrosis Disclosure Questionnaire.” 2015. Doctoral Dissertation, Virginia Commonwealth University. Accessed April 16, 2021. https://doi.org/10.25772/K3QW-K181 ; https://scholarscompass.vcu.edu/etd/4318.

MLA Handbook (7th Edition):

Borschuk, Adrienne P. “Scoring and Validation of the Cystic Fibrosis Disclosure Questionnaire.” 2015. Web. 16 Apr 2021.

Vancouver:

Borschuk AP. Scoring and Validation of the Cystic Fibrosis Disclosure Questionnaire. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2015. [cited 2021 Apr 16]. Available from: https://doi.org/10.25772/K3QW-K181 ; https://scholarscompass.vcu.edu/etd/4318.

Council of Science Editors:

Borschuk AP. Scoring and Validation of the Cystic Fibrosis Disclosure Questionnaire. [Doctoral Dissertation]. Virginia Commonwealth University; 2015. Available from: https://doi.org/10.25772/K3QW-K181 ; https://scholarscompass.vcu.edu/etd/4318


University of Toronto

11. 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 April 16, 2021. http://hdl.handle.net/1807/89009.

MLA Handbook (7th Edition):

Hung, Maurita. “The Development and Characterization of VX-770 Molecular Probes.” 2016. Web. 16 Apr 2021.

Vancouver:

Hung M. The Development and Characterization of VX-770 Molecular Probes. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2021 Apr 16]. 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


University of Cambridge

12. 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 April 16, 2021. 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. 16 Apr 2021.

Vancouver:

Rodriguez Rincon D. Tackling Mycobacterium abscessus infection in Cystic Fibrosis. [Internet] [Doctoral dissertation]. University of Cambridge; 2018. [cited 2021 Apr 16]. 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

13. 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 April 16, 2021. 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. 16 Apr 2021.

Vancouver:

Nasef HAHAR. Temperature modulated genosensor for detection of cystic fibrosis mutations. [Internet] [Thesis]. Universitat Rovira i Virgili; 2010. [cited 2021 Apr 16]. 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 Adelaide

14. 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 (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 April 16, 2021. 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. 16 Apr 2021.

Vancouver:

Kremer KL. Cystic Fibrosis gene therapy: methods for the optimisation of CFTR gene delivery. [Internet] [Thesis]. University of Adelaide; 2010. [cited 2021 Apr 16]. 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 Washington

15. 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 April 16, 2021. 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. 16 Apr 2021.

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 2021 Apr 16]. 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

16. 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 April 16, 2021. 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. 16 Apr 2021.

Vancouver:

LIDDY AM. The Pharmacokinetic Interaction between Ivacaftor and Ritonavir. [Internet] [Thesis]. Trinity College Dublin; 2019. [cited 2021 Apr 16]. 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


University of Manchester

17. 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 April 16, 2021. 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. 16 Apr 2021.

Vancouver:

Wells EJ. The role of parenting interventions in promoting treatment adherence in cystic fibrosis. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2021 Apr 16]. 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

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

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 April 16, 2021. 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. 16 Apr 2021.

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 2021 Apr 16]. 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


Laurentian University

19. 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 April 16, 2021. 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. 16 Apr 2021.

Vancouver:

Alhariri MAI. Evaluation of liposomal bismuth-ethanedithiol-tobramycin for treatment of cystic fibrosis pulmonary pseudomonas aeruginosa infection . [Internet] [Thesis]. Laurentian University; 2013. [cited 2021 Apr 16]. 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

20. 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

peer-reviewed

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… (more)

Subjects/Keywords: cystic fibrosis; CF; genetic testing

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

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 April 16, 2021. 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. 16 Apr 2021.

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 2021 Apr 16]. 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


Massey University

21. 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 April 16, 2021. 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. 16 Apr 2021.

Vancouver:

Doole PL. Getting on with life : the lived experience of four adults with cystic fibrosis. [Internet] [Masters thesis]. Massey University; 1996. [cited 2021 Apr 16]. 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 Louisville

22. 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 April 16, 2021. 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. 16 Apr 2021.

Vancouver:

Purdy ME. Recovery and biogeography of Pseudomonas and Burkholderia species from the human home. [Internet] [Doctoral dissertation]. University of Louisville; 2013. [cited 2021 Apr 16]. 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


Michigan State University

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

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 April 16, 2021. 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. 16 Apr 2021.

Vancouver:

Nickerson JM. Cellular and biochemical aspects of cystic fibrosis. [Internet] [Masters thesis]. Michigan State University; 1976. [cited 2021 Apr 16]. 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


University of Manchester

24. Lord, Robert William. Gastro-oeseophageal reflux and its relationship to cystic fibrosis lung disease.

Degree: 2019, University of Manchester

 Introduction: A number of studies have shown an increased prevalence of gastro-oesophageal reflux in adult and paediatric cystic fibrosis (CF) populations. To date it remains… (more)

Subjects/Keywords: Cystic fibrosis; Gastro-oesophageal reflux

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APA (6th Edition):

Lord, R. W. (2019). Gastro-oeseophageal reflux and its relationship to cystic fibrosis lung disease. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:319256

Chicago Manual of Style (16th Edition):

Lord, Robert William. “Gastro-oeseophageal reflux and its relationship to cystic fibrosis lung disease.” 2019. Doctoral Dissertation, University of Manchester. Accessed April 16, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:319256.

MLA Handbook (7th Edition):

Lord, Robert William. “Gastro-oeseophageal reflux and its relationship to cystic fibrosis lung disease.” 2019. Web. 16 Apr 2021.

Vancouver:

Lord RW. Gastro-oeseophageal reflux and its relationship to cystic fibrosis lung disease. [Internet] [Doctoral dissertation]. University of Manchester; 2019. [cited 2021 Apr 16]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:319256.

Council of Science Editors:

Lord RW. Gastro-oeseophageal reflux and its relationship to cystic fibrosis lung disease. [Doctoral Dissertation]. University of Manchester; 2019. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:319256


Rutgers University

25. 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 April 16, 2021. https://rucore.libraries.rutgers.edu/rutgers-lib/49245/.

MLA Handbook (7th Edition):

Kbah, Noor, 1987-. “Nanotechnology approach for treatment of cystic fibrosis.” 2016. Web. 16 Apr 2021.

Vancouver:

Kbah, Noor 1. Nanotechnology approach for treatment of cystic fibrosis. [Internet] [Masters thesis]. Rutgers University; 2016. [cited 2021 Apr 16]. 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/


Rutgers University

26. 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 April 16, 2021. 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. 16 Apr 2021.

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 2021 Apr 16]. 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/


University of Manchester

27. Lord, Robert. Gastro-oeseophageal reflux and its relationship to cystic fibrosis lung disease.

Degree: PhD, 2019, University of Manchester

 Introduction: A number of studies have shown an increased prevalence of gastro-oesophageal reflux in adult and paediatric cystic fibrosis (CF) populations. To date it remains… (more)

Subjects/Keywords: Gastro-oesophageal reflux; Cystic fibrosis

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

APA (6th Edition):

Lord, R. (2019). Gastro-oeseophageal reflux and its relationship to cystic fibrosis lung disease. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/gastrooeseophageal-reflux-and-its-relationship-to-cystic-fibrosis-lung-disease(99b28c27-76a3-452d-b838-e35405c4c051).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.823162

Chicago Manual of Style (16th Edition):

Lord, Robert. “Gastro-oeseophageal reflux and its relationship to cystic fibrosis lung disease.” 2019. Doctoral Dissertation, University of Manchester. Accessed April 16, 2021. https://www.research.manchester.ac.uk/portal/en/theses/gastrooeseophageal-reflux-and-its-relationship-to-cystic-fibrosis-lung-disease(99b28c27-76a3-452d-b838-e35405c4c051).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.823162.

MLA Handbook (7th Edition):

Lord, Robert. “Gastro-oeseophageal reflux and its relationship to cystic fibrosis lung disease.” 2019. Web. 16 Apr 2021.

Vancouver:

Lord R. Gastro-oeseophageal reflux and its relationship to cystic fibrosis lung disease. [Internet] [Doctoral dissertation]. University of Manchester; 2019. [cited 2021 Apr 16]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/gastrooeseophageal-reflux-and-its-relationship-to-cystic-fibrosis-lung-disease(99b28c27-76a3-452d-b838-e35405c4c051).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.823162.

Council of Science Editors:

Lord R. Gastro-oeseophageal reflux and its relationship to cystic fibrosis lung disease. [Doctoral Dissertation]. University of Manchester; 2019. Available from: https://www.research.manchester.ac.uk/portal/en/theses/gastrooeseophageal-reflux-and-its-relationship-to-cystic-fibrosis-lung-disease(99b28c27-76a3-452d-b838-e35405c4c051).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.823162


Ryerson University

28. 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 April 16, 2021. 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. 16 Apr 2021.

Vancouver:

Elmallah S. Progress Toward The Synthesis Of Labeled Derivatives Of The Cystic Fibrosis Drug Ivacaftor. [Internet] [Thesis]. Ryerson University; 2012. [cited 2021 Apr 16]. 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


University of Minnesota

29. 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 April 16, 2021. 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. 16 Apr 2021.

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 2021 Apr 16]. 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 Texas Southwestern Medical Center

30. Patrick, Anna Elizabeth. Cotranslational Folding of CFTR.

Degree: 2013, University of Texas Southwestern Medical Center

 The life of the cystic fibrosis transmembrane conductance regulator (CFTR) protein in the cell is dictated by its biogenesis, cellular trafficking, regulated function, and destruction.… (more)

Subjects/Keywords: Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Protein Folding

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

APA (6th Edition):

Patrick, A. E. (2013). Cotranslational Folding of CFTR. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/1704

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):

Patrick, Anna Elizabeth. “Cotranslational Folding of CFTR.” 2013. Thesis, University of Texas Southwestern Medical Center. Accessed April 16, 2021. http://hdl.handle.net/2152.5/1704.

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

MLA Handbook (7th Edition):

Patrick, Anna Elizabeth. “Cotranslational Folding of CFTR.” 2013. Web. 16 Apr 2021.

Vancouver:

Patrick AE. Cotranslational Folding of CFTR. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2013. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/2152.5/1704.

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

Council of Science Editors:

Patrick AE. Cotranslational Folding of CFTR. [Thesis]. University of Texas Southwestern Medical Center; 2013. Available from: http://hdl.handle.net/2152.5/1704

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

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