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You searched for subject:(pharmacokinetics). Showing records 1 – 30 of 1200 total matches.

[1] [2] [3] [4] [5] … [40]

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University of Georgia

1. Shen, Liang. preclinical pharmacokinetics and bioavailability studies of S-carboxymethylcysteine, N-acetylcysteine and (-)-carbodine.

Degree: PhD, Pharmacy, 2008, University of Georgia

 Bioavailability indicates the rate and extent of therapeutically active drug that reaches the systemic circulation and is available at the site of action. Bioavailability studies… (more)

Subjects/Keywords: Pharmacokinetics

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

APA (6th Edition):

Shen, L. (2008). preclinical pharmacokinetics and bioavailability studies of S-carboxymethylcysteine, N-acetylcysteine and (-)-carbodine. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/shen_liang_200812_phd

Chicago Manual of Style (16th Edition):

Shen, Liang. “preclinical pharmacokinetics and bioavailability studies of S-carboxymethylcysteine, N-acetylcysteine and (-)-carbodine.” 2008. Doctoral Dissertation, University of Georgia. Accessed February 18, 2020. http://purl.galileo.usg.edu/uga_etd/shen_liang_200812_phd.

MLA Handbook (7th Edition):

Shen, Liang. “preclinical pharmacokinetics and bioavailability studies of S-carboxymethylcysteine, N-acetylcysteine and (-)-carbodine.” 2008. Web. 18 Feb 2020.

Vancouver:

Shen L. preclinical pharmacokinetics and bioavailability studies of S-carboxymethylcysteine, N-acetylcysteine and (-)-carbodine. [Internet] [Doctoral dissertation]. University of Georgia; 2008. [cited 2020 Feb 18]. Available from: http://purl.galileo.usg.edu/uga_etd/shen_liang_200812_phd.

Council of Science Editors:

Shen L. preclinical pharmacokinetics and bioavailability studies of S-carboxymethylcysteine, N-acetylcysteine and (-)-carbodine. [Doctoral Dissertation]. University of Georgia; 2008. Available from: http://purl.galileo.usg.edu/uga_etd/shen_liang_200812_phd


University of Georgia

2. Zheng, Bo. Pharmacokinetic evaluation of investigational agents obtained from bioactive marine natural products, chemical synthesis and reformulation.

Degree: PhD, Pharmacy, 2009, University of Georgia

Pharmacokinetics is the science dedicated to the study of rate processes such as absorption, distribution, metabolism, and excretion (ADME) of a drug and the multiple… (more)

Subjects/Keywords: Pharmacokinetics

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APA (6th Edition):

Zheng, B. (2009). Pharmacokinetic evaluation of investigational agents obtained from bioactive marine natural products, chemical synthesis and reformulation. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/zheng_bo_200912_phd

Chicago Manual of Style (16th Edition):

Zheng, Bo. “Pharmacokinetic evaluation of investigational agents obtained from bioactive marine natural products, chemical synthesis and reformulation.” 2009. Doctoral Dissertation, University of Georgia. Accessed February 18, 2020. http://purl.galileo.usg.edu/uga_etd/zheng_bo_200912_phd.

MLA Handbook (7th Edition):

Zheng, Bo. “Pharmacokinetic evaluation of investigational agents obtained from bioactive marine natural products, chemical synthesis and reformulation.” 2009. Web. 18 Feb 2020.

Vancouver:

Zheng B. Pharmacokinetic evaluation of investigational agents obtained from bioactive marine natural products, chemical synthesis and reformulation. [Internet] [Doctoral dissertation]. University of Georgia; 2009. [cited 2020 Feb 18]. Available from: http://purl.galileo.usg.edu/uga_etd/zheng_bo_200912_phd.

Council of Science Editors:

Zheng B. Pharmacokinetic evaluation of investigational agents obtained from bioactive marine natural products, chemical synthesis and reformulation. [Doctoral Dissertation]. University of Georgia; 2009. Available from: http://purl.galileo.usg.edu/uga_etd/zheng_bo_200912_phd


Oregon State University

3. Tse, Sunny. The study of pharmacokinetics in a clinical environment.

Degree: PhD, Pharmacy, 2010, Oregon State University

 This dissertation presents a research series demonstrating the use of pharmacokinetic modeling and simulations as tools to assess drug concentration and disposition in patient populations.… (more)

Subjects/Keywords: pharmacokinetics; Pharmacokinetics  – Mathematical models

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APA (6th Edition):

Tse, S. (2010). The study of pharmacokinetics in a clinical environment. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/15037

Chicago Manual of Style (16th Edition):

Tse, Sunny. “The study of pharmacokinetics in a clinical environment.” 2010. Doctoral Dissertation, Oregon State University. Accessed February 18, 2020. http://hdl.handle.net/1957/15037.

MLA Handbook (7th Edition):

Tse, Sunny. “The study of pharmacokinetics in a clinical environment.” 2010. Web. 18 Feb 2020.

Vancouver:

Tse S. The study of pharmacokinetics in a clinical environment. [Internet] [Doctoral dissertation]. Oregon State University; 2010. [cited 2020 Feb 18]. Available from: http://hdl.handle.net/1957/15037.

Council of Science Editors:

Tse S. The study of pharmacokinetics in a clinical environment. [Doctoral Dissertation]. Oregon State University; 2010. Available from: http://hdl.handle.net/1957/15037


University of Georgia

4. Zhang, Weijiang. Pharmacokinetics of antiviral agents in veterinary medicine.

Degree: PhD, Pharmacy, 2002, University of Georgia

 The pharmacokinetics and brain distribution of zidovudine (3’-azido-3’-deoxythymidine, AZT) and lamivudine ((-)- 2’, 3’-dideoxy-3’-thiacytidine, 3TC) were investigated in healthy cats.|Plasma concentrations of AZT declined rapidly… (more)

Subjects/Keywords: Pharmacokinetics

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APA (6th Edition):

Zhang, W. (2002). Pharmacokinetics of antiviral agents in veterinary medicine. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/zhang_weijiang_200205_phd

Chicago Manual of Style (16th Edition):

Zhang, Weijiang. “Pharmacokinetics of antiviral agents in veterinary medicine.” 2002. Doctoral Dissertation, University of Georgia. Accessed February 18, 2020. http://purl.galileo.usg.edu/uga_etd/zhang_weijiang_200205_phd.

MLA Handbook (7th Edition):

Zhang, Weijiang. “Pharmacokinetics of antiviral agents in veterinary medicine.” 2002. Web. 18 Feb 2020.

Vancouver:

Zhang W. Pharmacokinetics of antiviral agents in veterinary medicine. [Internet] [Doctoral dissertation]. University of Georgia; 2002. [cited 2020 Feb 18]. Available from: http://purl.galileo.usg.edu/uga_etd/zhang_weijiang_200205_phd.

Council of Science Editors:

Zhang W. Pharmacokinetics of antiviral agents in veterinary medicine. [Doctoral Dissertation]. University of Georgia; 2002. Available from: http://purl.galileo.usg.edu/uga_etd/zhang_weijiang_200205_phd


University of Georgia

5. Lewis, Summer Renee. Maternal and fetal disposition of antiviral agents in the pregnant rat.

Degree: PhD, Pharmacy, 2006, University of Georgia

 Human immunodeficiency virus type-1 (HIV) infection has increased dramatically in pregnant women, thus, exposing the fetus in utero. However, with the increasing use of combination… (more)

Subjects/Keywords: Pharmacokinetics

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APA (6th Edition):

Lewis, S. R. (2006). Maternal and fetal disposition of antiviral agents in the pregnant rat. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/lewis_summer_r_200605_phd

Chicago Manual of Style (16th Edition):

Lewis, Summer Renee. “Maternal and fetal disposition of antiviral agents in the pregnant rat.” 2006. Doctoral Dissertation, University of Georgia. Accessed February 18, 2020. http://purl.galileo.usg.edu/uga_etd/lewis_summer_r_200605_phd.

MLA Handbook (7th Edition):

Lewis, Summer Renee. “Maternal and fetal disposition of antiviral agents in the pregnant rat.” 2006. Web. 18 Feb 2020.

Vancouver:

Lewis SR. Maternal and fetal disposition of antiviral agents in the pregnant rat. [Internet] [Doctoral dissertation]. University of Georgia; 2006. [cited 2020 Feb 18]. Available from: http://purl.galileo.usg.edu/uga_etd/lewis_summer_r_200605_phd.

Council of Science Editors:

Lewis SR. Maternal and fetal disposition of antiviral agents in the pregnant rat. [Doctoral Dissertation]. University of Georgia; 2006. Available from: http://purl.galileo.usg.edu/uga_etd/lewis_summer_r_200605_phd


University of Utah

6. Dean, Robin Rebecca. Opiate receptor down-regulation and tolerance;.

Degree: PhD, Pharmacology & Toxicology;, 1986, University of Utah

 The aim of the study was to investigate in the mouse the relationship between opiate-receptor down-regulation and opiate tolerance. Animals were treated for variable periods… (more)

Subjects/Keywords: Pharmacokinetics

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APA (6th Edition):

Dean, R. R. (1986). Opiate receptor down-regulation and tolerance;. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/620/rec/928

Chicago Manual of Style (16th Edition):

Dean, Robin Rebecca. “Opiate receptor down-regulation and tolerance;.” 1986. Doctoral Dissertation, University of Utah. Accessed February 18, 2020. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/620/rec/928.

MLA Handbook (7th Edition):

Dean, Robin Rebecca. “Opiate receptor down-regulation and tolerance;.” 1986. Web. 18 Feb 2020.

Vancouver:

Dean RR. Opiate receptor down-regulation and tolerance;. [Internet] [Doctoral dissertation]. University of Utah; 1986. [cited 2020 Feb 18]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/620/rec/928.

Council of Science Editors:

Dean RR. Opiate receptor down-regulation and tolerance;. [Doctoral Dissertation]. University of Utah; 1986. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/620/rec/928


Oregon State University

7. Tatong, Walapa. The evaluation of octanol-water partition coefficients from chromatographic data.

Degree: MS, Pharmacy, 1982, Oregon State University

 A set of 30 chemicals whose octanol-water partition coefficients (log P) are known were injected on a XAD-2 column and a commercially available octadecylsilane column.… (more)

Subjects/Keywords: Pharmacokinetics

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APA (6th Edition):

Tatong, W. (1982). The evaluation of octanol-water partition coefficients from chromatographic data. (Masters Thesis). Oregon State University. Retrieved from http://hdl.handle.net/1957/41743

Chicago Manual of Style (16th Edition):

Tatong, Walapa. “The evaluation of octanol-water partition coefficients from chromatographic data.” 1982. Masters Thesis, Oregon State University. Accessed February 18, 2020. http://hdl.handle.net/1957/41743.

MLA Handbook (7th Edition):

Tatong, Walapa. “The evaluation of octanol-water partition coefficients from chromatographic data.” 1982. Web. 18 Feb 2020.

Vancouver:

Tatong W. The evaluation of octanol-water partition coefficients from chromatographic data. [Internet] [Masters thesis]. Oregon State University; 1982. [cited 2020 Feb 18]. Available from: http://hdl.handle.net/1957/41743.

Council of Science Editors:

Tatong W. The evaluation of octanol-water partition coefficients from chromatographic data. [Masters Thesis]. Oregon State University; 1982. Available from: http://hdl.handle.net/1957/41743


Oregon State University

8. Kwon, Hyojong. Pharmacokinetic/pharmacodynamic modeling/simulation and novel gastric retention formulation.

Degree: PhD, Pharmacy, 2003, Oregon State University

 This dissertation describes formulation of a gastric retention device (GRD) and sustained release (SR) hydrochlorothiazide beads at Oregon State University. Formulation condition and amounts of… (more)

Subjects/Keywords: Pharmacokinetics

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APA (6th Edition):

Kwon, H. (2003). Pharmacokinetic/pharmacodynamic modeling/simulation and novel gastric retention formulation. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/32550

Chicago Manual of Style (16th Edition):

Kwon, Hyojong. “Pharmacokinetic/pharmacodynamic modeling/simulation and novel gastric retention formulation.” 2003. Doctoral Dissertation, Oregon State University. Accessed February 18, 2020. http://hdl.handle.net/1957/32550.

MLA Handbook (7th Edition):

Kwon, Hyojong. “Pharmacokinetic/pharmacodynamic modeling/simulation and novel gastric retention formulation.” 2003. Web. 18 Feb 2020.

Vancouver:

Kwon H. Pharmacokinetic/pharmacodynamic modeling/simulation and novel gastric retention formulation. [Internet] [Doctoral dissertation]. Oregon State University; 2003. [cited 2020 Feb 18]. Available from: http://hdl.handle.net/1957/32550.

Council of Science Editors:

Kwon H. Pharmacokinetic/pharmacodynamic modeling/simulation and novel gastric retention formulation. [Doctoral Dissertation]. Oregon State University; 2003. Available from: http://hdl.handle.net/1957/32550

9. Putthaporn Kaewmeesri. Effect of phyllanthus amarus schum. & thonn. extract on the pharmacokinetics of midazolam in rabbits .

Degree: คณะวิทยาศาสตร์ ภาควิชาเภสัชวิทยา, 2013, Prince of Songkla University

Subjects/Keywords: Pharmacokinetics

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APA (6th Edition):

Kaewmeesri, P. (2013). Effect of phyllanthus amarus schum. & thonn. extract on the pharmacokinetics of midazolam in rabbits . (Thesis). Prince of Songkla University. Retrieved from http://kb.psu.ac.th/psukb/handle/2010/9607

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):

Kaewmeesri, Putthaporn. “Effect of phyllanthus amarus schum. & thonn. extract on the pharmacokinetics of midazolam in rabbits .” 2013. Thesis, Prince of Songkla University. Accessed February 18, 2020. http://kb.psu.ac.th/psukb/handle/2010/9607.

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

MLA Handbook (7th Edition):

Kaewmeesri, Putthaporn. “Effect of phyllanthus amarus schum. & thonn. extract on the pharmacokinetics of midazolam in rabbits .” 2013. Web. 18 Feb 2020.

Vancouver:

Kaewmeesri P. Effect of phyllanthus amarus schum. & thonn. extract on the pharmacokinetics of midazolam in rabbits . [Internet] [Thesis]. Prince of Songkla University; 2013. [cited 2020 Feb 18]. Available from: http://kb.psu.ac.th/psukb/handle/2010/9607.

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

Council of Science Editors:

Kaewmeesri P. Effect of phyllanthus amarus schum. & thonn. extract on the pharmacokinetics of midazolam in rabbits . [Thesis]. Prince of Songkla University; 2013. Available from: http://kb.psu.ac.th/psukb/handle/2010/9607

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


University of Manitoba

10. Sayre, Casey L. Contribution of selected flavonoid enantiomers implicated in chronic disease prevention to differential pharmacokinetic and pharmacodynamic behaviour.

Degree: Pharmacy, 2013, University of Manitoba

 Decreases in risk of chronic disease associated with diets high in fruits and vegetables have been observed. Difficulty in determining the active ingredients responsible for… (more)

Subjects/Keywords: Pharmacokinetics; Flavonoid

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APA (6th Edition):

Sayre, C. L. (2013). Contribution of selected flavonoid enantiomers implicated in chronic disease prevention to differential pharmacokinetic and pharmacodynamic behaviour. (Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/30075

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):

Sayre, Casey L. “Contribution of selected flavonoid enantiomers implicated in chronic disease prevention to differential pharmacokinetic and pharmacodynamic behaviour.” 2013. Thesis, University of Manitoba. Accessed February 18, 2020. http://hdl.handle.net/1993/30075.

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

MLA Handbook (7th Edition):

Sayre, Casey L. “Contribution of selected flavonoid enantiomers implicated in chronic disease prevention to differential pharmacokinetic and pharmacodynamic behaviour.” 2013. Web. 18 Feb 2020.

Vancouver:

Sayre CL. Contribution of selected flavonoid enantiomers implicated in chronic disease prevention to differential pharmacokinetic and pharmacodynamic behaviour. [Internet] [Thesis]. University of Manitoba; 2013. [cited 2020 Feb 18]. Available from: http://hdl.handle.net/1993/30075.

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

Council of Science Editors:

Sayre CL. Contribution of selected flavonoid enantiomers implicated in chronic disease prevention to differential pharmacokinetic and pharmacodynamic behaviour. [Thesis]. University of Manitoba; 2013. Available from: http://hdl.handle.net/1993/30075

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


Rutgers University

11. Li, Xiaowan, 1991-. Physiologically based pharmacokinetic modeling of nanoparticles in rodents.

Degree: MS, Chemical and Biochemical Engineering, 2017, Rutgers University

 A variety of nanoparticles are under development for medicine, energy, food and cosmetics. Both organic and inorganic nanoparticles are playing an increased role in industrial… (more)

Subjects/Keywords: Pharmacokinetics; Nanoparticles

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APA (6th Edition):

Li, Xiaowan, 1. (2017). Physiologically based pharmacokinetic modeling of nanoparticles in rodents. (Masters Thesis). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/52225/

Chicago Manual of Style (16th Edition):

Li, Xiaowan, 1991-. “Physiologically based pharmacokinetic modeling of nanoparticles in rodents.” 2017. Masters Thesis, Rutgers University. Accessed February 18, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/52225/.

MLA Handbook (7th Edition):

Li, Xiaowan, 1991-. “Physiologically based pharmacokinetic modeling of nanoparticles in rodents.” 2017. Web. 18 Feb 2020.

Vancouver:

Li, Xiaowan 1. Physiologically based pharmacokinetic modeling of nanoparticles in rodents. [Internet] [Masters thesis]. Rutgers University; 2017. [cited 2020 Feb 18]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/52225/.

Council of Science Editors:

Li, Xiaowan 1. Physiologically based pharmacokinetic modeling of nanoparticles in rodents. [Masters Thesis]. Rutgers University; 2017. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/52225/


University of Arizona

12. Nelson, Owen A., 1951-. Pharmacokinetics modeling .

Degree: 1978, University of Arizona

Subjects/Keywords: Pharmacokinetics.

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APA (6th Edition):

Nelson, Owen A., 1. (1978). Pharmacokinetics modeling . (Masters Thesis). University of Arizona. Retrieved from http://hdl.handle.net/10150/348291

Chicago Manual of Style (16th Edition):

Nelson, Owen A., 1951-. “Pharmacokinetics modeling .” 1978. Masters Thesis, University of Arizona. Accessed February 18, 2020. http://hdl.handle.net/10150/348291.

MLA Handbook (7th Edition):

Nelson, Owen A., 1951-. “Pharmacokinetics modeling .” 1978. Web. 18 Feb 2020.

Vancouver:

Nelson, Owen A. 1. Pharmacokinetics modeling . [Internet] [Masters thesis]. University of Arizona; 1978. [cited 2020 Feb 18]. Available from: http://hdl.handle.net/10150/348291.

Council of Science Editors:

Nelson, Owen A. 1. Pharmacokinetics modeling . [Masters Thesis]. University of Arizona; 1978. Available from: http://hdl.handle.net/10150/348291


Université Catholique de Louvain

13. Guy-Viterbo, Vanessa. Toward individualization regimen of tacrolimus in pediatric liver transplantation.

Degree: 2019, Université Catholique de Louvain

Tacrolimus (Tac) is the cornerstone of immunosuppression in pediatric liver transplantation (PLT). However, its use is complicated by side effects and lack of efficacy partly… (more)

Subjects/Keywords: Population pharmacokinetics

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APA (6th Edition):

Guy-Viterbo, V. (2019). Toward individualization regimen of tacrolimus in pediatric liver transplantation. (Thesis). Université Catholique de Louvain. Retrieved from http://hdl.handle.net/2078.1/220246

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):

Guy-Viterbo, Vanessa. “Toward individualization regimen of tacrolimus in pediatric liver transplantation.” 2019. Thesis, Université Catholique de Louvain. Accessed February 18, 2020. http://hdl.handle.net/2078.1/220246.

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

MLA Handbook (7th Edition):

Guy-Viterbo, Vanessa. “Toward individualization regimen of tacrolimus in pediatric liver transplantation.” 2019. Web. 18 Feb 2020.

Vancouver:

Guy-Viterbo V. Toward individualization regimen of tacrolimus in pediatric liver transplantation. [Internet] [Thesis]. Université Catholique de Louvain; 2019. [cited 2020 Feb 18]. Available from: http://hdl.handle.net/2078.1/220246.

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

Council of Science Editors:

Guy-Viterbo V. Toward individualization regimen of tacrolimus in pediatric liver transplantation. [Thesis]. Université Catholique de Louvain; 2019. Available from: http://hdl.handle.net/2078.1/220246

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


University of Arizona

14. Acosta, Maria Fernanda. Advanced Design and Development of Novel Microparticulate/Nanoparticulate Dry Powder Inhalers for Targeted Treatment of Pulmonary Hypertension .

Degree: 2019, University of Arizona

 Pulmonary drug delivery is rapidly becoming one of the most important routes for targeting drugs to treat respiratory diseases. Pulmonary hypertension (PH) is a life-threatening… (more)

Subjects/Keywords: Pharmaceutics and Pharmacokinetics

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APA (6th Edition):

Acosta, M. F. (2019). Advanced Design and Development of Novel Microparticulate/Nanoparticulate Dry Powder Inhalers for Targeted Treatment of Pulmonary Hypertension . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/633218

Chicago Manual of Style (16th Edition):

Acosta, Maria Fernanda. “Advanced Design and Development of Novel Microparticulate/Nanoparticulate Dry Powder Inhalers for Targeted Treatment of Pulmonary Hypertension .” 2019. Doctoral Dissertation, University of Arizona. Accessed February 18, 2020. http://hdl.handle.net/10150/633218.

MLA Handbook (7th Edition):

Acosta, Maria Fernanda. “Advanced Design and Development of Novel Microparticulate/Nanoparticulate Dry Powder Inhalers for Targeted Treatment of Pulmonary Hypertension .” 2019. Web. 18 Feb 2020.

Vancouver:

Acosta MF. Advanced Design and Development of Novel Microparticulate/Nanoparticulate Dry Powder Inhalers for Targeted Treatment of Pulmonary Hypertension . [Internet] [Doctoral dissertation]. University of Arizona; 2019. [cited 2020 Feb 18]. Available from: http://hdl.handle.net/10150/633218.

Council of Science Editors:

Acosta MF. Advanced Design and Development of Novel Microparticulate/Nanoparticulate Dry Powder Inhalers for Targeted Treatment of Pulmonary Hypertension . [Doctoral Dissertation]. University of Arizona; 2019. Available from: http://hdl.handle.net/10150/633218


University of Illinois – Chicago

15. Justo, Julie Ann. Pharmacokinetics of Ceftaroline in Normal and Obese Subjects.

Degree: 2014, University of Illinois – Chicago

 The effect of obesity on the pharmacokinetics of ceftaroline (CPT) is currently unclear. This was a Phase I, open-label pharmacokinetic (PK) study performed in 32… (more)

Subjects/Keywords: ceftaroline; pharmacokinetics; obesity

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APA (6th Edition):

Justo, J. A. (2014). Pharmacokinetics of Ceftaroline in Normal and Obese Subjects. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/11298

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):

Justo, Julie Ann. “Pharmacokinetics of Ceftaroline in Normal and Obese Subjects.” 2014. Thesis, University of Illinois – Chicago. Accessed February 18, 2020. http://hdl.handle.net/10027/11298.

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

MLA Handbook (7th Edition):

Justo, Julie Ann. “Pharmacokinetics of Ceftaroline in Normal and Obese Subjects.” 2014. Web. 18 Feb 2020.

Vancouver:

Justo JA. Pharmacokinetics of Ceftaroline in Normal and Obese Subjects. [Internet] [Thesis]. University of Illinois – Chicago; 2014. [cited 2020 Feb 18]. Available from: http://hdl.handle.net/10027/11298.

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

Council of Science Editors:

Justo JA. Pharmacokinetics of Ceftaroline in Normal and Obese Subjects. [Thesis]. University of Illinois – Chicago; 2014. Available from: http://hdl.handle.net/10027/11298

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

16. Scherholz, Megerle, 1986-. Enabling personalized medicine through pharmacokinetic modeling.

Degree: PhD, Chemical and Biochemical Engineering, 2019, Rutgers University

 Personalized medicine strives to deliver the ‘right drug’ at the ‘right dose’ at the ‘right time’ by considering the unique characteristics that define specialized populations… (more)

Subjects/Keywords: Pharmacokinetics; Personalized medicine

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APA (6th Edition):

Scherholz, Megerle, 1. (2019). Enabling personalized medicine through pharmacokinetic modeling. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/60057/

Chicago Manual of Style (16th Edition):

Scherholz, Megerle, 1986-. “Enabling personalized medicine through pharmacokinetic modeling.” 2019. Doctoral Dissertation, Rutgers University. Accessed February 18, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/60057/.

MLA Handbook (7th Edition):

Scherholz, Megerle, 1986-. “Enabling personalized medicine through pharmacokinetic modeling.” 2019. Web. 18 Feb 2020.

Vancouver:

Scherholz, Megerle 1. Enabling personalized medicine through pharmacokinetic modeling. [Internet] [Doctoral dissertation]. Rutgers University; 2019. [cited 2020 Feb 18]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/60057/.

Council of Science Editors:

Scherholz, Megerle 1. Enabling personalized medicine through pharmacokinetic modeling. [Doctoral Dissertation]. Rutgers University; 2019. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/60057/


The Ohio State University

17. Kirsch, Lee E. In vitro and in vivo prodrug conversion kinetics of cyclocytidine to cytarabine, an antileukemic drug.

Degree: PhD, Graduate School, 1982, The Ohio State University

Subjects/Keywords: Chemistry; Pharmacokinetics

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APA (6th Edition):

Kirsch, L. E. (1982). In vitro and in vivo prodrug conversion kinetics of cyclocytidine to cytarabine, an antileukemic drug. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1487236343857118

Chicago Manual of Style (16th Edition):

Kirsch, Lee E. “In vitro and in vivo prodrug conversion kinetics of cyclocytidine to cytarabine, an antileukemic drug.” 1982. Doctoral Dissertation, The Ohio State University. Accessed February 18, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487236343857118.

MLA Handbook (7th Edition):

Kirsch, Lee E. “In vitro and in vivo prodrug conversion kinetics of cyclocytidine to cytarabine, an antileukemic drug.” 1982. Web. 18 Feb 2020.

Vancouver:

Kirsch LE. In vitro and in vivo prodrug conversion kinetics of cyclocytidine to cytarabine, an antileukemic drug. [Internet] [Doctoral dissertation]. The Ohio State University; 1982. [cited 2020 Feb 18]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1487236343857118.

Council of Science Editors:

Kirsch LE. In vitro and in vivo prodrug conversion kinetics of cyclocytidine to cytarabine, an antileukemic drug. [Doctoral Dissertation]. The Ohio State University; 1982. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1487236343857118


The Ohio State University

18. Yang, Joanna Yee. Study of Michaelis-Menton equation with applications in pharmacokinetics.

Degree: PhD, Graduate School, 1977, The Ohio State University

Subjects/Keywords: Biology; Pharmacokinetics

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APA (6th Edition):

Yang, J. Y. (1977). Study of Michaelis-Menton equation with applications in pharmacokinetics. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1487069564240539

Chicago Manual of Style (16th Edition):

Yang, Joanna Yee. “Study of Michaelis-Menton equation with applications in pharmacokinetics.” 1977. Doctoral Dissertation, The Ohio State University. Accessed February 18, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487069564240539.

MLA Handbook (7th Edition):

Yang, Joanna Yee. “Study of Michaelis-Menton equation with applications in pharmacokinetics.” 1977. Web. 18 Feb 2020.

Vancouver:

Yang JY. Study of Michaelis-Menton equation with applications in pharmacokinetics. [Internet] [Doctoral dissertation]. The Ohio State University; 1977. [cited 2020 Feb 18]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1487069564240539.

Council of Science Editors:

Yang JY. Study of Michaelis-Menton equation with applications in pharmacokinetics. [Doctoral Dissertation]. The Ohio State University; 1977. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1487069564240539


University of Utah

19. Gross, Garrett John. Effects of pentylenetetrazol on ion transport in the isolated toad bladder;.

Degree: PhD, Pharmacology & Toxicology;, 1972, University of Utah

 The effect of pentylenetetrazol (PTZ) on ion transport in the isolated toad bladder was investigated. PTZ produced an increase in short-circuit current (SCC) when placed… (more)

Subjects/Keywords: Pharmacokinetics; Toads

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APA (6th Edition):

Gross, G. J. (1972). Effects of pentylenetetrazol on ion transport in the isolated toad bladder;. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/174/rec/430

Chicago Manual of Style (16th Edition):

Gross, Garrett John. “Effects of pentylenetetrazol on ion transport in the isolated toad bladder;.” 1972. Doctoral Dissertation, University of Utah. Accessed February 18, 2020. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/174/rec/430.

MLA Handbook (7th Edition):

Gross, Garrett John. “Effects of pentylenetetrazol on ion transport in the isolated toad bladder;.” 1972. Web. 18 Feb 2020.

Vancouver:

Gross GJ. Effects of pentylenetetrazol on ion transport in the isolated toad bladder;. [Internet] [Doctoral dissertation]. University of Utah; 1972. [cited 2020 Feb 18]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/174/rec/430.

Council of Science Editors:

Gross GJ. Effects of pentylenetetrazol on ion transport in the isolated toad bladder;. [Doctoral Dissertation]. University of Utah; 1972. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/174/rec/430


University of Utah

20. Winters, Suzanne. Immobilized heparin via a long chain poly(ethylene oxide) spacer for protein and platelet compatibility;.

Degree: PhD, Pharmaceutics & Pharmaceutical Chemistry;, 1987, University of Utah

 Poly(ethylene oxide) has some unique solubility and hydrogen-bonding characteristics which have been used to explain its apparent inertness with regard to blood protein absorption and… (more)

Subjects/Keywords: Pharmacokinetics; Biosynthesis

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APA (6th Edition):

Winters, S. (1987). Immobilized heparin via a long chain poly(ethylene oxide) spacer for protein and platelet compatibility;. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/523/rec/646

Chicago Manual of Style (16th Edition):

Winters, Suzanne. “Immobilized heparin via a long chain poly(ethylene oxide) spacer for protein and platelet compatibility;.” 1987. Doctoral Dissertation, University of Utah. Accessed February 18, 2020. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/523/rec/646.

MLA Handbook (7th Edition):

Winters, Suzanne. “Immobilized heparin via a long chain poly(ethylene oxide) spacer for protein and platelet compatibility;.” 1987. Web. 18 Feb 2020.

Vancouver:

Winters S. Immobilized heparin via a long chain poly(ethylene oxide) spacer for protein and platelet compatibility;. [Internet] [Doctoral dissertation]. University of Utah; 1987. [cited 2020 Feb 18]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/523/rec/646.

Council of Science Editors:

Winters S. Immobilized heparin via a long chain poly(ethylene oxide) spacer for protein and platelet compatibility;. [Doctoral Dissertation]. University of Utah; 1987. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/523/rec/646


University of Utah

21. Webb, Jerry Glen. Effects of stimulation on intracellular calcium in frog sartorius muscle;.

Degree: PhD, Pharmacology & Toxicology;, 1972, University of Utah

 The cellular state and distribution of calcium were investigated in frog sartorius muscle at rest and following periods of stimulation. The purpose of the experiments… (more)

Subjects/Keywords: Metabolism; Pharmacokinetics

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APA (6th Edition):

Webb, J. G. (1972). Effects of stimulation on intracellular calcium in frog sartorius muscle;. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/988/rec/433

Chicago Manual of Style (16th Edition):

Webb, Jerry Glen. “Effects of stimulation on intracellular calcium in frog sartorius muscle;.” 1972. Doctoral Dissertation, University of Utah. Accessed February 18, 2020. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/988/rec/433.

MLA Handbook (7th Edition):

Webb, Jerry Glen. “Effects of stimulation on intracellular calcium in frog sartorius muscle;.” 1972. Web. 18 Feb 2020.

Vancouver:

Webb JG. Effects of stimulation on intracellular calcium in frog sartorius muscle;. [Internet] [Doctoral dissertation]. University of Utah; 1972. [cited 2020 Feb 18]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/988/rec/433.

Council of Science Editors:

Webb JG. Effects of stimulation on intracellular calcium in frog sartorius muscle;. [Doctoral Dissertation]. University of Utah; 1972. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/988/rec/433


University of Utah

22. Lin, Ching-Shan. Pharmacokinetic study of uterine progesterone retention;.

Degree: PhD, Pharmaceutics & Pharmaceutical Chemistry;, 1997, University of Utah

 Tritium-labeled progesterone was administered to mature female rate in the proestrous stage of three different routes, gastric intubation, subcutaneous injection, and uterine intraluminal instillation, to… (more)

Subjects/Keywords: Pharmacokinetics; Receptors

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APA (6th Edition):

Lin, C. (1997). Pharmacokinetic study of uterine progesterone retention;. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1012/rec/971

Chicago Manual of Style (16th Edition):

Lin, Ching-Shan. “Pharmacokinetic study of uterine progesterone retention;.” 1997. Doctoral Dissertation, University of Utah. Accessed February 18, 2020. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1012/rec/971.

MLA Handbook (7th Edition):

Lin, Ching-Shan. “Pharmacokinetic study of uterine progesterone retention;.” 1997. Web. 18 Feb 2020.

Vancouver:

Lin C. Pharmacokinetic study of uterine progesterone retention;. [Internet] [Doctoral dissertation]. University of Utah; 1997. [cited 2020 Feb 18]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1012/rec/971.

Council of Science Editors:

Lin C. Pharmacokinetic study of uterine progesterone retention;. [Doctoral Dissertation]. University of Utah; 1997. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1012/rec/971


University of Utah

23. Brondsted, Helle. Hydrogels for colon-specific peptide drug delivery;.

Degree: PhD, Pharmaceutics & Pharmaceutical Chemistry;, 1991, University of Utah

 Novel hydrogels based on hydrophilic N-substituted (meth)acrylamides, N-tert-butylacrylamide and acrylic acid crosslinked with azoaromatic compounds of varying length and electron density of the azo bond… (more)

Subjects/Keywords: Pharmacology; Pharmacokinetics

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APA (6th Edition):

Brondsted, H. (1991). Hydrogels for colon-specific peptide drug delivery;. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1461/rec/628

Chicago Manual of Style (16th Edition):

Brondsted, Helle. “Hydrogels for colon-specific peptide drug delivery;.” 1991. Doctoral Dissertation, University of Utah. Accessed February 18, 2020. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1461/rec/628.

MLA Handbook (7th Edition):

Brondsted, Helle. “Hydrogels for colon-specific peptide drug delivery;.” 1991. Web. 18 Feb 2020.

Vancouver:

Brondsted H. Hydrogels for colon-specific peptide drug delivery;. [Internet] [Doctoral dissertation]. University of Utah; 1991. [cited 2020 Feb 18]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1461/rec/628.

Council of Science Editors:

Brondsted H. Hydrogels for colon-specific peptide drug delivery;. [Doctoral Dissertation]. University of Utah; 1991. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1461/rec/628


University of Utah

24. Christensen, John Mark. A Physiological pharmacokinetic model for norethindrone.

Degree: PhD, Pharmaceutics & Pharmaceutical Chemistry;, 1980, University of Utah

 Physiological pharmacokinetic models are derived from basic considerations of physiological, anatomical, and pharmacologic principles. These modes can simultaneously predict drug levels in blood, organs, and… (more)

Subjects/Keywords: Pharmacology; Pharmacokinetics

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APA (6th Edition):

Christensen, J. M. (1980). A Physiological pharmacokinetic model for norethindrone. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1109/rec/32

Chicago Manual of Style (16th Edition):

Christensen, John Mark. “A Physiological pharmacokinetic model for norethindrone.” 1980. Doctoral Dissertation, University of Utah. Accessed February 18, 2020. http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1109/rec/32.

MLA Handbook (7th Edition):

Christensen, John Mark. “A Physiological pharmacokinetic model for norethindrone.” 1980. Web. 18 Feb 2020.

Vancouver:

Christensen JM. A Physiological pharmacokinetic model for norethindrone. [Internet] [Doctoral dissertation]. University of Utah; 1980. [cited 2020 Feb 18]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1109/rec/32.

Council of Science Editors:

Christensen JM. A Physiological pharmacokinetic model for norethindrone. [Doctoral Dissertation]. University of Utah; 1980. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1109/rec/32


University of Utah

25. Lim, Heng-Keang. Metabolism of 3,4-(Methylenedioxy)-methamphetamine;.

Degree: PhD, Pharmacology & Toxicology;, 1989, University of Utah

 (RS)-3,4-(Methylenedioxy)methamphetamine (MDMA) is a ring-substituted amphetamine derivative, hence its common reference in the literature as a 'designer drug.' With respect to its pharmacology, MDMA is… (more)

Subjects/Keywords: Pharmacokinetics; Metabolites

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APA (6th Edition):

Lim, H. (1989). Metabolism of 3,4-(Methylenedioxy)-methamphetamine;. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1669/rec/807

Chicago Manual of Style (16th Edition):

Lim, Heng-Keang. “Metabolism of 3,4-(Methylenedioxy)-methamphetamine;.” 1989. Doctoral Dissertation, University of Utah. Accessed February 18, 2020. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1669/rec/807.

MLA Handbook (7th Edition):

Lim, Heng-Keang. “Metabolism of 3,4-(Methylenedioxy)-methamphetamine;.” 1989. Web. 18 Feb 2020.

Vancouver:

Lim H. Metabolism of 3,4-(Methylenedioxy)-methamphetamine;. [Internet] [Doctoral dissertation]. University of Utah; 1989. [cited 2020 Feb 18]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1669/rec/807.

Council of Science Editors:

Lim H. Metabolism of 3,4-(Methylenedioxy)-methamphetamine;. [Doctoral Dissertation]. University of Utah; 1989. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1669/rec/807


University of Alberta

26. Yau, Manfred S. L. Kinetic characteristics of lidocaine during prolonged infusion - a study using perfused rat liver.

Degree: MS, Faculty of Pharmacy and Pharmaceutical Sciences, 1986, University of Alberta

Subjects/Keywords: Lidocaine – Pharmacokinetics.

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APA (6th Edition):

Yau, M. S. L. (1986). Kinetic characteristics of lidocaine during prolonged infusion - a study using perfused rat liver. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/zg64tn757

Chicago Manual of Style (16th Edition):

Yau, Manfred S L. “Kinetic characteristics of lidocaine during prolonged infusion - a study using perfused rat liver.” 1986. Masters Thesis, University of Alberta. Accessed February 18, 2020. https://era.library.ualberta.ca/files/zg64tn757.

MLA Handbook (7th Edition):

Yau, Manfred S L. “Kinetic characteristics of lidocaine during prolonged infusion - a study using perfused rat liver.” 1986. Web. 18 Feb 2020.

Vancouver:

Yau MSL. Kinetic characteristics of lidocaine during prolonged infusion - a study using perfused rat liver. [Internet] [Masters thesis]. University of Alberta; 1986. [cited 2020 Feb 18]. Available from: https://era.library.ualberta.ca/files/zg64tn757.

Council of Science Editors:

Yau MSL. Kinetic characteristics of lidocaine during prolonged infusion - a study using perfused rat liver. [Masters Thesis]. University of Alberta; 1986. Available from: https://era.library.ualberta.ca/files/zg64tn757


University of Alberta

27. Ibrahim, Alyaa, EA. Absorption and Bioavailability of Glucosamine in the Rat.

Degree: PhD, Faculty of Pharmacy and Pharmaceutical Sciences, 2012, University of Alberta

 Glucosamine (GlcN) is an amino monosaccharide that is widely used as a food supplement in the treatment of osteoarthritis (OA). In vitro and animal studies… (more)

Subjects/Keywords: Bioavailability; Pharmacokinetics; Glucosamine; Absorption

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APA (6th Edition):

Ibrahim, Alyaa, E. (2012). Absorption and Bioavailability of Glucosamine in the Rat. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/gt54kn19s

Chicago Manual of Style (16th Edition):

Ibrahim, Alyaa, EA. “Absorption and Bioavailability of Glucosamine in the Rat.” 2012. Doctoral Dissertation, University of Alberta. Accessed February 18, 2020. https://era.library.ualberta.ca/files/gt54kn19s.

MLA Handbook (7th Edition):

Ibrahim, Alyaa, EA. “Absorption and Bioavailability of Glucosamine in the Rat.” 2012. Web. 18 Feb 2020.

Vancouver:

Ibrahim, Alyaa E. Absorption and Bioavailability of Glucosamine in the Rat. [Internet] [Doctoral dissertation]. University of Alberta; 2012. [cited 2020 Feb 18]. Available from: https://era.library.ualberta.ca/files/gt54kn19s.

Council of Science Editors:

Ibrahim, Alyaa E. Absorption and Bioavailability of Glucosamine in the Rat. [Doctoral Dissertation]. University of Alberta; 2012. Available from: https://era.library.ualberta.ca/files/gt54kn19s


University of Alberta

28. Alessi-Severini, Silvia. Racemic pharmaceuticals: analysis and pharmacokinetics of flecainide and methocarbamol enantiomers.

Degree: PhD, Faculty of Pharmacy and Pharmaceutical Sciences, 1993, University of Alberta

Subjects/Keywords: Enantiomers – Pharmacokinetics.

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APA (6th Edition):

Alessi-Severini, S. (1993). Racemic pharmaceuticals: analysis and pharmacokinetics of flecainide and methocarbamol enantiomers. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/hx11xh84d

Chicago Manual of Style (16th Edition):

Alessi-Severini, Silvia. “Racemic pharmaceuticals: analysis and pharmacokinetics of flecainide and methocarbamol enantiomers.” 1993. Doctoral Dissertation, University of Alberta. Accessed February 18, 2020. https://era.library.ualberta.ca/files/hx11xh84d.

MLA Handbook (7th Edition):

Alessi-Severini, Silvia. “Racemic pharmaceuticals: analysis and pharmacokinetics of flecainide and methocarbamol enantiomers.” 1993. Web. 18 Feb 2020.

Vancouver:

Alessi-Severini S. Racemic pharmaceuticals: analysis and pharmacokinetics of flecainide and methocarbamol enantiomers. [Internet] [Doctoral dissertation]. University of Alberta; 1993. [cited 2020 Feb 18]. Available from: https://era.library.ualberta.ca/files/hx11xh84d.

Council of Science Editors:

Alessi-Severini S. Racemic pharmaceuticals: analysis and pharmacokinetics of flecainide and methocarbamol enantiomers. [Doctoral Dissertation]. University of Alberta; 1993. Available from: https://era.library.ualberta.ca/files/hx11xh84d


Laurentian University

29. Chenard, Pamela. A comparison of doxorubicin and doxorubicinol in rat heart and liver tissue following anthracycline administration .

Degree: 2015, Laurentian University

 This study examined the pharmacokinetic profile of the chemotherapeutic drug doxorubicin (DOX), and of its main metabolite doxorubicinol (DOXOL) in male Sprague-Dawley rats. HPLC was… (more)

Subjects/Keywords: Doxorubicin pharmacokinetics; Doxorubicin; Doxorubicinol; Chromatography

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APA (6th Edition):

Chenard, P. (2015). A comparison of doxorubicin and doxorubicinol in rat heart and liver tissue following anthracycline administration . (Thesis). Laurentian University. Retrieved from https://zone.biblio.laurentian.ca/dspace/handle/10219/2423

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):

Chenard, Pamela. “A comparison of doxorubicin and doxorubicinol in rat heart and liver tissue following anthracycline administration .” 2015. Thesis, Laurentian University. Accessed February 18, 2020. https://zone.biblio.laurentian.ca/dspace/handle/10219/2423.

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

MLA Handbook (7th Edition):

Chenard, Pamela. “A comparison of doxorubicin and doxorubicinol in rat heart and liver tissue following anthracycline administration .” 2015. Web. 18 Feb 2020.

Vancouver:

Chenard P. A comparison of doxorubicin and doxorubicinol in rat heart and liver tissue following anthracycline administration . [Internet] [Thesis]. Laurentian University; 2015. [cited 2020 Feb 18]. Available from: https://zone.biblio.laurentian.ca/dspace/handle/10219/2423.

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

Council of Science Editors:

Chenard P. A comparison of doxorubicin and doxorubicinol in rat heart and liver tissue following anthracycline administration . [Thesis]. Laurentian University; 2015. Available from: https://zone.biblio.laurentian.ca/dspace/handle/10219/2423

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


University of KwaZulu-Natal

30. [No author]. Modelling the interaction between human immunodeficiency virus, mycobacterium tuberculosis and the human immune system, including the effects of drug therapy.

Degree: 2007, University of KwaZulu-Natal

 Tuberculosis (TB) is the leading cause of death in individuals infected with human immunodeficiency virus (HIV) in several African countries, including South Africa. HIV-positive individuals… (more)

Subjects/Keywords: Pharmacology.; Chemistry – Pharmacokinetics.; Drug evaluation.

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APA (6th Edition):

author], [. (2007). Modelling the interaction between human immunodeficiency virus, mycobacterium tuberculosis and the human immune system, including the effects of drug therapy. (Thesis). University of KwaZulu-Natal. Retrieved from http://hdl.handle.net/10413/1056

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):

author], [No. “Modelling the interaction between human immunodeficiency virus, mycobacterium tuberculosis and the human immune system, including the effects of drug therapy. ” 2007. Thesis, University of KwaZulu-Natal. Accessed February 18, 2020. http://hdl.handle.net/10413/1056.

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

MLA Handbook (7th Edition):

author], [No. “Modelling the interaction between human immunodeficiency virus, mycobacterium tuberculosis and the human immune system, including the effects of drug therapy. ” 2007. Web. 18 Feb 2020.

Vancouver:

author] [. Modelling the interaction between human immunodeficiency virus, mycobacterium tuberculosis and the human immune system, including the effects of drug therapy. [Internet] [Thesis]. University of KwaZulu-Natal; 2007. [cited 2020 Feb 18]. Available from: http://hdl.handle.net/10413/1056.

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

Council of Science Editors:

author] [. Modelling the interaction between human immunodeficiency virus, mycobacterium tuberculosis and the human immune system, including the effects of drug therapy. [Thesis]. University of KwaZulu-Natal; 2007. Available from: http://hdl.handle.net/10413/1056

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

[1] [2] [3] [4] [5] … [40]

.