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You searched for subject:( population pharmacokinetic). Showing records 1 – 18 of 18 total matches.

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1. Munshi, Reema Mohammad. Exploring population pharmacokinetic models in patients treated with vancomycin during continuous venovenous hemodiafiltration on different anticoagulant modalities.

Degree: School of Pharmacy & Pharma. Sciences. Discipline of Pharmacy, 2017, Trinity College Dublin

 Uncertainty remains concerning pharmacokinetics (PK) of antimicrobials in critically ill patients due to the scarcity of data and the variable physiology of the patient cohort.… (more)

Subjects/Keywords: population pharmacokinetic; continuous venovenous hemodiafiltration

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

APA (6th Edition):

Munshi, R. M. (2017). Exploring population pharmacokinetic models in patients treated with vancomycin during continuous venovenous hemodiafiltration on different anticoagulant modalities. (Thesis). Trinity College Dublin. Retrieved from http://hdl.handle.net/2262/81724

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):

Munshi, Reema Mohammad. “Exploring population pharmacokinetic models in patients treated with vancomycin during continuous venovenous hemodiafiltration on different anticoagulant modalities.” 2017. Thesis, Trinity College Dublin. Accessed September 16, 2019. http://hdl.handle.net/2262/81724.

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

MLA Handbook (7th Edition):

Munshi, Reema Mohammad. “Exploring population pharmacokinetic models in patients treated with vancomycin during continuous venovenous hemodiafiltration on different anticoagulant modalities.” 2017. Web. 16 Sep 2019.

Vancouver:

Munshi RM. Exploring population pharmacokinetic models in patients treated with vancomycin during continuous venovenous hemodiafiltration on different anticoagulant modalities. [Internet] [Thesis]. Trinity College Dublin; 2017. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/2262/81724.

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

Council of Science Editors:

Munshi RM. Exploring population pharmacokinetic models in patients treated with vancomycin during continuous venovenous hemodiafiltration on different anticoagulant modalities. [Thesis]. Trinity College Dublin; 2017. Available from: http://hdl.handle.net/2262/81724

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


University of Southern California

2. Hsu, Joy C. Animal to human scaling and pharmacokinetic/pharmacodynamic modeling of anticancer drugs.

Degree: PhD, Biomedical Engineering, 2009, University of Southern California

 Three major interspecies scaling approaches are analyzed and the predictive performance for each of these scaling methods in estimating human systemic clearance, volume of distribution… (more)

Subjects/Keywords: interspecies scaling; allometric scaling; physiologically based pharmacokinetic (PBPK) model scaling; population compartmental model scaling; pharmacokinetic-tumor pharmacodynamic modeling; indirect response models; feedback autoregulatory models; population pharmacokinetic analysis

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APA (6th Edition):

Hsu, J. C. (2009). Animal to human scaling and pharmacokinetic/pharmacodynamic modeling of anticancer drugs. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/215593/rec/830

Chicago Manual of Style (16th Edition):

Hsu, Joy C. “Animal to human scaling and pharmacokinetic/pharmacodynamic modeling of anticancer drugs.” 2009. Doctoral Dissertation, University of Southern California. Accessed September 16, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/215593/rec/830.

MLA Handbook (7th Edition):

Hsu, Joy C. “Animal to human scaling and pharmacokinetic/pharmacodynamic modeling of anticancer drugs.” 2009. Web. 16 Sep 2019.

Vancouver:

Hsu JC. Animal to human scaling and pharmacokinetic/pharmacodynamic modeling of anticancer drugs. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2019 Sep 16]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/215593/rec/830.

Council of Science Editors:

Hsu JC. Animal to human scaling and pharmacokinetic/pharmacodynamic modeling of anticancer drugs. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/215593/rec/830


Univerzitet u Beogradu

3. Brzaković, Branka R. Farmakokinetička varijabilnost lamotrigina kod dece i adolescenata na kombinovanoj terapiji za lečenje epilepsije.

Degree: Farmaceutski fakultet, 2016, Univerzitet u Beogradu

Farmacija - Farmakokinetika i klinička farmacija / Pharmacy - Pharmacokinetics and Clinical Pharmacy

Lamotrigin (LTG) se kod dece i adolescenata često koristi kao adjuvantna terapija… (more)

Subjects/Keywords: pharmacokinetic variability; population model; therapeutic drug monitoring; lamotrigine; epilepsy

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APA (6th Edition):

Brzaković, B. R. (2016). Farmakokinetička varijabilnost lamotrigina kod dece i adolescenata na kombinovanoj terapiji za lečenje epilepsije. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:12787/bdef:Content/get

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):

Brzaković, Branka R. “Farmakokinetička varijabilnost lamotrigina kod dece i adolescenata na kombinovanoj terapiji za lečenje epilepsije.” 2016. Thesis, Univerzitet u Beogradu. Accessed September 16, 2019. https://fedorabg.bg.ac.rs/fedora/get/o:12787/bdef:Content/get.

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

MLA Handbook (7th Edition):

Brzaković, Branka R. “Farmakokinetička varijabilnost lamotrigina kod dece i adolescenata na kombinovanoj terapiji za lečenje epilepsije.” 2016. Web. 16 Sep 2019.

Vancouver:

Brzaković BR. Farmakokinetička varijabilnost lamotrigina kod dece i adolescenata na kombinovanoj terapiji za lečenje epilepsije. [Internet] [Thesis]. Univerzitet u Beogradu; 2016. [cited 2019 Sep 16]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:12787/bdef:Content/get.

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

Council of Science Editors:

Brzaković BR. Farmakokinetička varijabilnost lamotrigina kod dece i adolescenata na kombinovanoj terapiji za lečenje epilepsije. [Thesis]. Univerzitet u Beogradu; 2016. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:12787/bdef:Content/get

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


Iowa State University

4. Sun, Xiaoyong. Diagnostics for nonlinear models with application to population pharmacokinetic modeling.

Degree: 2010, Iowa State University

 Biological problems often involve fitting nonlinear models to data. In pharmacokinetics, analysts study a subject's response to drug doses, which will typically follow a quick… (more)

Subjects/Keywords: Interactive graphics; Model diagnostics; Population pharmacokinetic model; Resampling statistics; Visualization

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APA (6th Edition):

Sun, X. (2010). Diagnostics for nonlinear models with application to population pharmacokinetic modeling. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/11468

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):

Sun, Xiaoyong. “Diagnostics for nonlinear models with application to population pharmacokinetic modeling.” 2010. Thesis, Iowa State University. Accessed September 16, 2019. https://lib.dr.iastate.edu/etd/11468.

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

MLA Handbook (7th Edition):

Sun, Xiaoyong. “Diagnostics for nonlinear models with application to population pharmacokinetic modeling.” 2010. Web. 16 Sep 2019.

Vancouver:

Sun X. Diagnostics for nonlinear models with application to population pharmacokinetic modeling. [Internet] [Thesis]. Iowa State University; 2010. [cited 2019 Sep 16]. Available from: https://lib.dr.iastate.edu/etd/11468.

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

Council of Science Editors:

Sun X. Diagnostics for nonlinear models with application to population pharmacokinetic modeling. [Thesis]. Iowa State University; 2010. Available from: https://lib.dr.iastate.edu/etd/11468

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


Univerzitet u Beogradu

5. Голубовић, Бојана, 1983- 16767335. Популациони приступ фармакокинетичкој анализи такролимуса и сиролимуса у пацијената са трансплантираним бубрегом.

Degree: Farmaceutski fakultet, 2019, Univerzitet u Beogradu

Фармација - Фармакокинетика и клиничка фармација / Pharmacy - Pharmacokinetics and Clinical Pharmacy

Циљ докторске дисертације био је да се применом популационе фармакокинетичке анализе идентификују… (more)

Subjects/Keywords: immunosuppressive drugs; therapy individualization; population modeling; therapeutic monitoring; pharmacokinetic variability; pharmacometrics

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APA (6th Edition):

Голубовић, Бојана, 1. 1. (2019). Популациони приступ фармакокинетичкој анализи такролимуса и сиролимуса у пацијената са трансплантираним бубрегом. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:19903/bdef:Content/get

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):

Голубовић, Бојана, 1983- 16767335. “Популациони приступ фармакокинетичкој анализи такролимуса и сиролимуса у пацијената са трансплантираним бубрегом.” 2019. Thesis, Univerzitet u Beogradu. Accessed September 16, 2019. https://fedorabg.bg.ac.rs/fedora/get/o:19903/bdef:Content/get.

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

MLA Handbook (7th Edition):

Голубовић, Бојана, 1983- 16767335. “Популациони приступ фармакокинетичкој анализи такролимуса и сиролимуса у пацијената са трансплантираним бубрегом.” 2019. Web. 16 Sep 2019.

Vancouver:

Голубовић, Бојана 11. Популациони приступ фармакокинетичкој анализи такролимуса и сиролимуса у пацијената са трансплантираним бубрегом. [Internet] [Thesis]. Univerzitet u Beogradu; 2019. [cited 2019 Sep 16]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:19903/bdef:Content/get.

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

Council of Science Editors:

Голубовић, Бојана 11. Популациони приступ фармакокинетичкој анализи такролимуса и сиролимуса у пацијената са трансплантираним бубрегом. [Thesis]. Univerzitet u Beogradu; 2019. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:19903/bdef:Content/get

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


University of Manchester

6. Wendling, Thierry. Hierarchical mechanistic modelling of clinical pharmacokinetic data.

Degree: PhD, 2016, University of Manchester

Pharmacokinetic and pharmacodynamic models can be applied to clinical study data using various modelling approaches depending on the aim of the analysis. In population pharmacokinetics… (more)

Subjects/Keywords: 615.7; Pharmacokinetic modelling; Population approach; Bayesian statistics; Physiologically-based pharmacokinetic models; Mavoglurant; Clinical data; Survival analysis; Pancreatic cancer

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

APA (6th Edition):

Wendling, T. (2016). Hierarchical mechanistic modelling of clinical pharmacokinetic data. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/hierarchical-mechanistic-modelling-of-clinical-pharmacokinetic-data(573652c9-d3fb-4233-bea7-7abd7ef48d4b).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.684798

Chicago Manual of Style (16th Edition):

Wendling, Thierry. “Hierarchical mechanistic modelling of clinical pharmacokinetic data.” 2016. Doctoral Dissertation, University of Manchester. Accessed September 16, 2019. https://www.research.manchester.ac.uk/portal/en/theses/hierarchical-mechanistic-modelling-of-clinical-pharmacokinetic-data(573652c9-d3fb-4233-bea7-7abd7ef48d4b).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.684798.

MLA Handbook (7th Edition):

Wendling, Thierry. “Hierarchical mechanistic modelling of clinical pharmacokinetic data.” 2016. Web. 16 Sep 2019.

Vancouver:

Wendling T. Hierarchical mechanistic modelling of clinical pharmacokinetic data. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2019 Sep 16]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/hierarchical-mechanistic-modelling-of-clinical-pharmacokinetic-data(573652c9-d3fb-4233-bea7-7abd7ef48d4b).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.684798.

Council of Science Editors:

Wendling T. Hierarchical mechanistic modelling of clinical pharmacokinetic data. [Doctoral Dissertation]. University of Manchester; 2016. Available from: https://www.research.manchester.ac.uk/portal/en/theses/hierarchical-mechanistic-modelling-of-clinical-pharmacokinetic-data(573652c9-d3fb-4233-bea7-7abd7ef48d4b).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.684798

7. Wendling, Thierry. Hierarchical mechanistic modelling of clinical pharmacokinetic data.

Degree: 2016, University of Manchester

Pharmacokinetic and pharmacodynamic models can be applied to clinical study data using various modelling approaches depending on the aim of the analysis. In population pharmacokinetics… (more)

Subjects/Keywords: Pharmacokinetic modelling; Population approach; Bayesian statistics; Physiologically-based pharmacokinetic models; Mavoglurant; Clinical data; Survival analysis; Pancreatic cancer

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

APA (6th Edition):

Wendling, T. (2016). Hierarchical mechanistic modelling of clinical pharmacokinetic data. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:296912

Chicago Manual of Style (16th Edition):

Wendling, Thierry. “Hierarchical mechanistic modelling of clinical pharmacokinetic data.” 2016. Doctoral Dissertation, University of Manchester. Accessed September 16, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:296912.

MLA Handbook (7th Edition):

Wendling, Thierry. “Hierarchical mechanistic modelling of clinical pharmacokinetic data.” 2016. Web. 16 Sep 2019.

Vancouver:

Wendling T. Hierarchical mechanistic modelling of clinical pharmacokinetic data. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2019 Sep 16]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:296912.

Council of Science Editors:

Wendling T. Hierarchical mechanistic modelling of clinical pharmacokinetic data. [Doctoral Dissertation]. University of Manchester; 2016. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:296912


University of Sydney

8. Upadhyay, Parth. Pharmacokinetic, Pharmacodynamic and Pharmacogenetic Factors Associated with Busulfan Clinical Pharmacology .

Degree: 2019, University of Sydney

 Busulfan is a bifunctional alkylating agent used in combination with other chemotherapeutics for the ablation of dysfunctional bone marrow prior to haematopoietic stem cell transplantation.… (more)

Subjects/Keywords: busulfan; Sinusoidal Obstruction Syndrome (SOS); NONMEM; haematopoietic stem cell transplantation (HSCT); population-pharmacokinetic

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APA (6th Edition):

Upadhyay, P. (2019). Pharmacokinetic, Pharmacodynamic and Pharmacogenetic Factors Associated with Busulfan Clinical Pharmacology . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/20490

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):

Upadhyay, Parth. “Pharmacokinetic, Pharmacodynamic and Pharmacogenetic Factors Associated with Busulfan Clinical Pharmacology .” 2019. Thesis, University of Sydney. Accessed September 16, 2019. http://hdl.handle.net/2123/20490.

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

MLA Handbook (7th Edition):

Upadhyay, Parth. “Pharmacokinetic, Pharmacodynamic and Pharmacogenetic Factors Associated with Busulfan Clinical Pharmacology .” 2019. Web. 16 Sep 2019.

Vancouver:

Upadhyay P. Pharmacokinetic, Pharmacodynamic and Pharmacogenetic Factors Associated with Busulfan Clinical Pharmacology . [Internet] [Thesis]. University of Sydney; 2019. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/2123/20490.

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

Council of Science Editors:

Upadhyay P. Pharmacokinetic, Pharmacodynamic and Pharmacogenetic Factors Associated with Busulfan Clinical Pharmacology . [Thesis]. University of Sydney; 2019. Available from: http://hdl.handle.net/2123/20490

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

9. Peigné, Sophie. Evaluation et comparaison de méthodologies pharmacocinétiques en pédiatrie : Human genetics of clinical forms of leprosy.

Degree: Docteur es, Pharmacologie, 2015, Sorbonne Paris Cité

Un nouveau règlement (CE) n° 1901/2006 établi par le Parlement européen et le Conseil de l’UE, relatif aux médicaments à usage pédiatrique, vise à améliorer… (more)

Subjects/Keywords: Ivabradine; Pédiatrie; Préparation d’une étude; Méthode dried blood spot; Approche physiologique; Modélisation pharmacocinétique de population; Allométrie; Fonction de maturation; Relation pharmacocinétique / pharmacodynamique; Ivabradine; Paediatric; Study preparation; Dried blood spot; Physiologically-based Pharmacokinetic; Population pharmacokinetic modelling; Allometric scaling; Maturation function; Pharmacokinetic / pharmacodynamic relationship; 615.108 3

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APA (6th Edition):

Peigné, S. (2015). Evaluation et comparaison de méthodologies pharmacocinétiques en pédiatrie : Human genetics of clinical forms of leprosy. (Doctoral Dissertation). Sorbonne Paris Cité. Retrieved from http://www.theses.fr/2015USPCB146

Chicago Manual of Style (16th Edition):

Peigné, Sophie. “Evaluation et comparaison de méthodologies pharmacocinétiques en pédiatrie : Human genetics of clinical forms of leprosy.” 2015. Doctoral Dissertation, Sorbonne Paris Cité. Accessed September 16, 2019. http://www.theses.fr/2015USPCB146.

MLA Handbook (7th Edition):

Peigné, Sophie. “Evaluation et comparaison de méthodologies pharmacocinétiques en pédiatrie : Human genetics of clinical forms of leprosy.” 2015. Web. 16 Sep 2019.

Vancouver:

Peigné S. Evaluation et comparaison de méthodologies pharmacocinétiques en pédiatrie : Human genetics of clinical forms of leprosy. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; 2015. [cited 2019 Sep 16]. Available from: http://www.theses.fr/2015USPCB146.

Council of Science Editors:

Peigné S. Evaluation et comparaison de méthodologies pharmacocinétiques en pédiatrie : Human genetics of clinical forms of leprosy. [Doctoral Dissertation]. Sorbonne Paris Cité; 2015. Available from: http://www.theses.fr/2015USPCB146


Universidade do Rio Grande do Sul

10. Nava, Tiago Rodrigues. Modelo de personalização de dose de bussulfano intravenoso baseado no genótipo de GSTA1 durante regime de condicionamento do transplante de células-tronco hematopoiéticas em crianças.

Degree: 2017, Universidade do Rio Grande do Sul

 O bussulfano (Bu) é um agente alquilante usado no condicionamento que precede o transplante de células-tronco hematopoiéticas (TCTH) em crianças. Sua farmacocinética (FC) apresenta uma… (more)

Subjects/Keywords: Hematopoietic stem cell transplantation; Transplante de células-tronco hematopoéticas; Bussulfano; Population pharmacokinetic model; Farmacogenética; GSTA1; Polymorphisms; Farmacocinética; Parmacogenetics; Pharmacokinetics; Busulfan; HSCT

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

APA (6th Edition):

Nava, T. R. (2017). Modelo de personalização de dose de bussulfano intravenoso baseado no genótipo de GSTA1 durante regime de condicionamento do transplante de células-tronco hematopoiéticas em crianças. (Thesis). Universidade do Rio Grande do Sul. Retrieved from http://hdl.handle.net/10183/169580

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):

Nava, Tiago Rodrigues. “Modelo de personalização de dose de bussulfano intravenoso baseado no genótipo de GSTA1 durante regime de condicionamento do transplante de células-tronco hematopoiéticas em crianças.” 2017. Thesis, Universidade do Rio Grande do Sul. Accessed September 16, 2019. http://hdl.handle.net/10183/169580.

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

MLA Handbook (7th Edition):

Nava, Tiago Rodrigues. “Modelo de personalização de dose de bussulfano intravenoso baseado no genótipo de GSTA1 durante regime de condicionamento do transplante de células-tronco hematopoiéticas em crianças.” 2017. Web. 16 Sep 2019.

Vancouver:

Nava TR. Modelo de personalização de dose de bussulfano intravenoso baseado no genótipo de GSTA1 durante regime de condicionamento do transplante de células-tronco hematopoiéticas em crianças. [Internet] [Thesis]. Universidade do Rio Grande do Sul; 2017. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/10183/169580.

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

Council of Science Editors:

Nava TR. Modelo de personalização de dose de bussulfano intravenoso baseado no genótipo de GSTA1 durante regime de condicionamento do transplante de células-tronco hematopoiéticas em crianças. [Thesis]. Universidade do Rio Grande do Sul; 2017. Available from: http://hdl.handle.net/10183/169580

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


University of Iowa

11. Bi, Youwei. Population pharmacokinetic/pharmacodynamic (PK/PD) modeling of depot testosterone cypionate in healthy male subjects.

Degree: PhD, Pharmaceutical Sciences and Experimental Therapeutics, 2016, University of Iowa

  Depot intramuscularly administered testosterone cypionate (TC) is indicated for treatment of hypogonadism in males. However, illegal use of TC and other anabolic steroids in… (more)

Subjects/Keywords: Abuse of steroids; Luteinizing hormone; Population pharmacokinetic/pharmacodynamic (PK/PD) modeling; Spermatogenesis; Testosterone cypionate; Pharmacy and Pharmaceutical Sciences

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

APA (6th Edition):

Bi, Y. (2016). Population pharmacokinetic/pharmacodynamic (PK/PD) modeling of depot testosterone cypionate in healthy male subjects. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/5716

Chicago Manual of Style (16th Edition):

Bi, Youwei. “Population pharmacokinetic/pharmacodynamic (PK/PD) modeling of depot testosterone cypionate in healthy male subjects.” 2016. Doctoral Dissertation, University of Iowa. Accessed September 16, 2019. https://ir.uiowa.edu/etd/5716.

MLA Handbook (7th Edition):

Bi, Youwei. “Population pharmacokinetic/pharmacodynamic (PK/PD) modeling of depot testosterone cypionate in healthy male subjects.” 2016. Web. 16 Sep 2019.

Vancouver:

Bi Y. Population pharmacokinetic/pharmacodynamic (PK/PD) modeling of depot testosterone cypionate in healthy male subjects. [Internet] [Doctoral dissertation]. University of Iowa; 2016. [cited 2019 Sep 16]. Available from: https://ir.uiowa.edu/etd/5716.

Council of Science Editors:

Bi Y. Population pharmacokinetic/pharmacodynamic (PK/PD) modeling of depot testosterone cypionate in healthy male subjects. [Doctoral Dissertation]. University of Iowa; 2016. Available from: https://ir.uiowa.edu/etd/5716


University of Florida

12. Wu, Benjamin. Utilizing Mechanism-Based Pharmacokinetic and Pharmacodynamic Models to Understand and Overcome Antibiotic Resistance.

Degree: PhD, Pharmaceutical Sciences - Pharmaceutics, 2010, University of Florida

 The emergence of antimicrobial resistance poses a critical challenge to public health in the 21st century. The current practice to treat microbes relies on single… (more)

Subjects/Keywords: Antimicrobials; Dosage; Drug design; Modeling; Parametric models; Plasmas; Population estimates; Population growth rate; Resistance mechanisms; Statistical models; antimicrobial, ciprofloxacin, dynamic, mechanism, pharmacodynamic, pharmacokinetic, pseudonomas

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APA (6th Edition):

Wu, B. (2010). Utilizing Mechanism-Based Pharmacokinetic and Pharmacodynamic Models to Understand and Overcome Antibiotic Resistance. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0042293

Chicago Manual of Style (16th Edition):

Wu, Benjamin. “Utilizing Mechanism-Based Pharmacokinetic and Pharmacodynamic Models to Understand and Overcome Antibiotic Resistance.” 2010. Doctoral Dissertation, University of Florida. Accessed September 16, 2019. http://ufdc.ufl.edu/UFE0042293.

MLA Handbook (7th Edition):

Wu, Benjamin. “Utilizing Mechanism-Based Pharmacokinetic and Pharmacodynamic Models to Understand and Overcome Antibiotic Resistance.” 2010. Web. 16 Sep 2019.

Vancouver:

Wu B. Utilizing Mechanism-Based Pharmacokinetic and Pharmacodynamic Models to Understand and Overcome Antibiotic Resistance. [Internet] [Doctoral dissertation]. University of Florida; 2010. [cited 2019 Sep 16]. Available from: http://ufdc.ufl.edu/UFE0042293.

Council of Science Editors:

Wu B. Utilizing Mechanism-Based Pharmacokinetic and Pharmacodynamic Models to Understand and Overcome Antibiotic Resistance. [Doctoral Dissertation]. University of Florida; 2010. Available from: http://ufdc.ufl.edu/UFE0042293

13. Imbert, Bruce. Pharmacologie du baclofène et applications cliniques en addictologie : Pharmacology and clinical applications of baclofen in addiction.

Degree: Docteur es, Pathologie humaine, 2016, Aix Marseille Université

L’objectif principal de nos études a été de caractériser la pharmacocinétique du baclofène chez le patient alcoolo-dépendant et d’étudier la variation du craving en fonction… (more)

Subjects/Keywords: Baclofène; Troubles de l’usage de l’alcool; Alcoolo-Dépendance; Craving; Pharmacocinétique de population.; Baclofen; Alcohol-Use disorder; Alcohol-Dependence; Craving for alcohol; Population pharmacokinetic.

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APA (6th Edition):

Imbert, B. (2016). Pharmacologie du baclofène et applications cliniques en addictologie : Pharmacology and clinical applications of baclofen in addiction. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2016AIXM5047

Chicago Manual of Style (16th Edition):

Imbert, Bruce. “Pharmacologie du baclofène et applications cliniques en addictologie : Pharmacology and clinical applications of baclofen in addiction.” 2016. Doctoral Dissertation, Aix Marseille Université. Accessed September 16, 2019. http://www.theses.fr/2016AIXM5047.

MLA Handbook (7th Edition):

Imbert, Bruce. “Pharmacologie du baclofène et applications cliniques en addictologie : Pharmacology and clinical applications of baclofen in addiction.” 2016. Web. 16 Sep 2019.

Vancouver:

Imbert B. Pharmacologie du baclofène et applications cliniques en addictologie : Pharmacology and clinical applications of baclofen in addiction. [Internet] [Doctoral dissertation]. Aix Marseille Université 2016. [cited 2019 Sep 16]. Available from: http://www.theses.fr/2016AIXM5047.

Council of Science Editors:

Imbert B. Pharmacologie du baclofène et applications cliniques en addictologie : Pharmacology and clinical applications of baclofen in addiction. [Doctoral Dissertation]. Aix Marseille Université 2016. Available from: http://www.theses.fr/2016AIXM5047


University of Pretoria

14. Dodgen, Tyren Mark. Pharmacogenetics of CYP2D6 and CYP2C19 as a pre-prescription tool for drug efficacy and toxicity in a demographically-representative sample of theSouth African population.

Degree: Pharmacology, 2014, University of Pretoria

 The Cytochrome P450 family of enzymes is responsible for the majority of Phase I metabolism, and has been identified as an important source of pharmacokinetic(more)

Subjects/Keywords: Pharmacokinetic; Therapeutic; Treatment response; Drug reactions; South African population; Pharmacogenetics of CYP2C19; Pharmacogenetics of CYP2D6; The Food and Drug Administration; FDA; UCTD

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APA (6th Edition):

Dodgen, T. M. (2014). Pharmacogenetics of CYP2D6 and CYP2C19 as a pre-prescription tool for drug efficacy and toxicity in a demographically-representative sample of theSouth African population. (Doctoral Dissertation). University of Pretoria. Retrieved from http://hdl.handle.net/2263/33242

Chicago Manual of Style (16th Edition):

Dodgen, Tyren Mark. “Pharmacogenetics of CYP2D6 and CYP2C19 as a pre-prescription tool for drug efficacy and toxicity in a demographically-representative sample of theSouth African population.” 2014. Doctoral Dissertation, University of Pretoria. Accessed September 16, 2019. http://hdl.handle.net/2263/33242.

MLA Handbook (7th Edition):

Dodgen, Tyren Mark. “Pharmacogenetics of CYP2D6 and CYP2C19 as a pre-prescription tool for drug efficacy and toxicity in a demographically-representative sample of theSouth African population.” 2014. Web. 16 Sep 2019.

Vancouver:

Dodgen TM. Pharmacogenetics of CYP2D6 and CYP2C19 as a pre-prescription tool for drug efficacy and toxicity in a demographically-representative sample of theSouth African population. [Internet] [Doctoral dissertation]. University of Pretoria; 2014. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/2263/33242.

Council of Science Editors:

Dodgen TM. Pharmacogenetics of CYP2D6 and CYP2C19 as a pre-prescription tool for drug efficacy and toxicity in a demographically-representative sample of theSouth African population. [Doctoral Dissertation]. University of Pretoria; 2014. Available from: http://hdl.handle.net/2263/33242


Université de Montréal

15. Grenier, Julie. Optimisation de l'utilisation des techniques de modélisation dans le passage de l'étape pré-clinique à clinique du développement d'un médicament .

Degree: 2009, Université de Montréal

Subjects/Keywords: Pharmacocinétique; Pharmacokinetic; Population; Population; Physiologique; Physiological; Cyclosporine; Cyclosporine; Allométrie; Allometry; Absorption intestinale; Intestional absorption; P-gp; P-gp; CYP3A; CYP3A

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APA (6th Edition):

Grenier, J. (2009). Optimisation de l'utilisation des techniques de modélisation dans le passage de l'étape pré-clinique à clinique du développement d'un médicament . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/6686

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):

Grenier, Julie. “Optimisation de l'utilisation des techniques de modélisation dans le passage de l'étape pré-clinique à clinique du développement d'un médicament .” 2009. Thesis, Université de Montréal. Accessed September 16, 2019. http://hdl.handle.net/1866/6686.

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

MLA Handbook (7th Edition):

Grenier, Julie. “Optimisation de l'utilisation des techniques de modélisation dans le passage de l'étape pré-clinique à clinique du développement d'un médicament .” 2009. Web. 16 Sep 2019.

Vancouver:

Grenier J. Optimisation de l'utilisation des techniques de modélisation dans le passage de l'étape pré-clinique à clinique du développement d'un médicament . [Internet] [Thesis]. Université de Montréal; 2009. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/1866/6686.

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

Council of Science Editors:

Grenier J. Optimisation de l'utilisation des techniques de modélisation dans le passage de l'étape pré-clinique à clinique du développement d'un médicament . [Thesis]. Université de Montréal; 2009. Available from: http://hdl.handle.net/1866/6686

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


University of Florida

16. Sy, Sherwin K. Dosing Strategies of Antibiotic Combinations to Overcome Resistance.

Degree: PhD, Pharmaceutical Sciences - Pharmaceutics, 2014, University of Florida

Subjects/Keywords: Antimicrobials; ATMs; Bacteria; Drug design; In vitro fertilization; Kinetics; Lactams; Modeling; Population estimates; Population growth rate; antimicrobial; combination; pharmacodynamic; pharmacokinetic; pharmacometrics

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APA (6th Edition):

Sy, S. K. (2014). Dosing Strategies of Antibiotic Combinations to Overcome Resistance. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0046554

Chicago Manual of Style (16th Edition):

Sy, Sherwin K. “Dosing Strategies of Antibiotic Combinations to Overcome Resistance.” 2014. Doctoral Dissertation, University of Florida. Accessed September 16, 2019. http://ufdc.ufl.edu/UFE0046554.

MLA Handbook (7th Edition):

Sy, Sherwin K. “Dosing Strategies of Antibiotic Combinations to Overcome Resistance.” 2014. Web. 16 Sep 2019.

Vancouver:

Sy SK. Dosing Strategies of Antibiotic Combinations to Overcome Resistance. [Internet] [Doctoral dissertation]. University of Florida; 2014. [cited 2019 Sep 16]. Available from: http://ufdc.ufl.edu/UFE0046554.

Council of Science Editors:

Sy SK. Dosing Strategies of Antibiotic Combinations to Overcome Resistance. [Doctoral Dissertation]. University of Florida; 2014. Available from: http://ufdc.ufl.edu/UFE0046554


Universiteit Utrecht

17. Attema-de Jonge, M.E. (Milly Ellen). Pharmacokinetically guided dosing of (high-dose) chemotherapeutic agents.

Degree: 2004, Universiteit Utrecht

 Due to variation in drug distribution, metabolism and elimination processes between patients, systemic exposure to chemotherapeutic agents may be highly variable from patient to patient… (more)

Subjects/Keywords: Farmacie; Cyclophosphamide; thiotepa; carboplatin; paclitaxel; dose-individualization; pharmacokinetically guided dosing; population pharmacokinetics; metabolism; high-dose chemotherapy; pharmacokinetic-pharmacodynamic relationships

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

APA (6th Edition):

Attema-de Jonge, M. E. (. E. (2004). Pharmacokinetically guided dosing of (high-dose) chemotherapeutic agents. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/1245

Chicago Manual of Style (16th Edition):

Attema-de Jonge, M E (Milly Ellen). “Pharmacokinetically guided dosing of (high-dose) chemotherapeutic agents.” 2004. Doctoral Dissertation, Universiteit Utrecht. Accessed September 16, 2019. http://dspace.library.uu.nl:8080/handle/1874/1245.

MLA Handbook (7th Edition):

Attema-de Jonge, M E (Milly Ellen). “Pharmacokinetically guided dosing of (high-dose) chemotherapeutic agents.” 2004. Web. 16 Sep 2019.

Vancouver:

Attema-de Jonge ME(E. Pharmacokinetically guided dosing of (high-dose) chemotherapeutic agents. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2004. [cited 2019 Sep 16]. Available from: http://dspace.library.uu.nl:8080/handle/1874/1245.

Council of Science Editors:

Attema-de Jonge ME(E. Pharmacokinetically guided dosing of (high-dose) chemotherapeutic agents. [Doctoral Dissertation]. Universiteit Utrecht; 2004. Available from: http://dspace.library.uu.nl:8080/handle/1874/1245

18. Attema-de Jonge, M.E. (Milly Ellen). Pharmacokinetically guided dosing of (high-dose) chemotherapeutic agents.

Degree: 2004, University Utrecht

 Due to variation in drug distribution, metabolism and elimination processes between patients, systemic exposure to chemotherapeutic agents may be highly variable from patient to patient… (more)

Subjects/Keywords: Cyclophosphamide; thiotepa; carboplatin; paclitaxel; dose-individualization; pharmacokinetically guided dosing; population pharmacokinetics; metabolism; high-dose chemotherapy; pharmacokinetic-pharmacodynamic relationships

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

APA (6th Edition):

Attema-de Jonge, M. E. (. E. (2004). Pharmacokinetically guided dosing of (high-dose) chemotherapeutic agents. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/1245 ; URN:NBN:NL:UI:10-1874-1245 ; urn:isbn:90-9018807-X ; URN:NBN:NL:UI:10-1874-1245 ; http://dspace.library.uu.nl/handle/1874/1245

Chicago Manual of Style (16th Edition):

Attema-de Jonge, M E (Milly Ellen). “Pharmacokinetically guided dosing of (high-dose) chemotherapeutic agents.” 2004. Doctoral Dissertation, University Utrecht. Accessed September 16, 2019. http://dspace.library.uu.nl/handle/1874/1245 ; URN:NBN:NL:UI:10-1874-1245 ; urn:isbn:90-9018807-X ; URN:NBN:NL:UI:10-1874-1245 ; http://dspace.library.uu.nl/handle/1874/1245.

MLA Handbook (7th Edition):

Attema-de Jonge, M E (Milly Ellen). “Pharmacokinetically guided dosing of (high-dose) chemotherapeutic agents.” 2004. Web. 16 Sep 2019.

Vancouver:

Attema-de Jonge ME(E. Pharmacokinetically guided dosing of (high-dose) chemotherapeutic agents. [Internet] [Doctoral dissertation]. University Utrecht; 2004. [cited 2019 Sep 16]. Available from: http://dspace.library.uu.nl/handle/1874/1245 ; URN:NBN:NL:UI:10-1874-1245 ; urn:isbn:90-9018807-X ; URN:NBN:NL:UI:10-1874-1245 ; http://dspace.library.uu.nl/handle/1874/1245.

Council of Science Editors:

Attema-de Jonge ME(E. Pharmacokinetically guided dosing of (high-dose) chemotherapeutic agents. [Doctoral Dissertation]. University Utrecht; 2004. Available from: http://dspace.library.uu.nl/handle/1874/1245 ; URN:NBN:NL:UI:10-1874-1245 ; urn:isbn:90-9018807-X ; URN:NBN:NL:UI:10-1874-1245 ; http://dspace.library.uu.nl/handle/1874/1245

.