Therapeutic Drug Monitoring of Ganciclovir: Where Are We?-Reference-Cited by-同舟云学术

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Therapeutic Drug Monitoring of Ganciclovir: Where Are We?

Published:2021-10-05 Issue:1 Volume:44 Page:138-147
ISSN:0163-4356
Container-title:Therapeutic Drug Monitoring
language:en
Short-container-title:

Author:

Märtson Anne-Grete,Edwina Angela E.,Kim Hannah Yejin,Knoester Marjolein,Touw Daan J.,Sturkenboom Marieke G. G.,Alffenaar Jan-Willem C.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Pharmacology (medical),Pharmacology

Reference83 articles.

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2. The third international consensus guidelines on the management of cytomegalovirus in solid-organ transplantation;Kotton;Transplantation,2018

3. Human herpesvirus 6, 7, and 8 in solid organ transplantation: guidelines from the american society of transplantation infectious diseases community of practice;Pellett Madan;Clin Transpl,2019

4. Antiviral therapy (Non-HIV);Beigel;Goldman’s Cecil Med,2012

5. Metabolic activation of the nucleoside analog 9-[( 2-hydroxy-1-(hydroxymethyl)ethoxy]methyl)guanine in human diploid fibroblasts infected with human cytomegalovirus;Biron;Proc Natl Acad Sci U S A,1985

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1. Cytomegalovirus in haematopoietic cell transplantation - The troll is still there;Best Practice & Research Clinical Haematology;2024-09

2. Application of machine-learning models to predict the ganciclovir and valganciclovir exposure in children using a limited sampling strategy;Antimicrobial Agents and Chemotherapy;2024-08-28

3. The pharmacokinetics of ganciclovir during prolonged intermittent kidney replacement therapy in a cardiac transplant recipient;Journal of Chemotherapy;2024-08-26

4. Assessment of Dried Serum Spots (DSS) and Volumetric-Absorptive Microsampling (VAMS) Techniques in Therapeutic Drug Monitoring of (Val)Ganciclovir—Comparative Study in Analytical and Clinical Practice;International Journal of Molecular Sciences;2024-08-12

5. Recommendations for the selection of nucleoside analogues as antihuman herpesvirus drugs: a real-world analysis of reported cases from the FDA adverse event reporting system;Expert Opinion on Drug Safety;2024-07-04

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