Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Jieluan Lu"'
Autor:
Xianhuan Shen, Xuejuan Li, Jieluan Lu, Jiahao Zhu, Yaodong He, Zhou Zhang, Zebin Chen, Jianping Zhang, Xiaomei Fan, Wenzhou Li
Publikováno v:
CPT: Pharmacometrics & Systems Pharmacology, Vol 13, Iss 7, Pp 1201-1213 (2024)
Abstract Changes in physiological factors may result in large pharmacokinetic variability of vancomycin in pediatric patients, thereby leading to either supratherapeutic or subtherapeutic exposure and potentially affecting clinical outcomes. This stu
Externí odkaz:
https://doaj.org/article/7662b775404940ea9803064ca21e0aa0
Autor:
Jiahao Zhu, Jieluan Lu, Yaodong He, Xianhuan Shen, Hanbing Xia, Wenzhou Li, Jianping Zhang, Xiaomei Fan
Publikováno v:
Pharmaceuticals, Vol 16, Iss 11, p 1536 (2023)
Genetic polymorphisms in ATP-binding cassette subfamily B member 1 (ABCB1, also known as MDR1) have been reported to be possibly associated with the regulation of response to antiseizure medications. The aim of this study was to investigate the assoc
Externí odkaz:
https://doaj.org/article/9c5f671673364092b5bbf148fbae6f01
Autor:
Xianhuan Shen, Xinyi Chen, Jieluan Lu, Qing Chen, Wenzhou Li, Jiahao Zhu, Yaodong He, Huijuan Guo, Chenshu Xu, Xiaomei Fan
Publikováno v:
Frontiers in Pharmacology, Vol 13 (2022)
Objective: The aim of this study was to establish a population pharmacokinetic (PPK) model of valproic acid (VPA) in pediatric patients with epilepsy in southern China, and provide guidance for individualized medication of VPA therapy.Methods: A tota
Externí odkaz:
https://doaj.org/article/9ca70a3aa5ab49099c97feb3462e2856
Autor:
Xiaomei Fan, Yuna Chen, Jieluan Lu, Wenzhou Li, Xi Li, Huijuan Guo, Qing Chen, Yanxia Yang, Hanbing Xia
Publikováno v:
Frontiers in Neuroscience, Vol 15 (2021)
Epilepsy is a common neurologic disorder characterized by intractable seizures, involving genetic factors. There is a need to develop reliable genetic markers to predict the risk of epilepsy and design effective therapies. Arsenite methyltransferase
Externí odkaz:
https://doaj.org/article/ae857dbca95240709fa2ab3170de95fc
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Background: Erythema multiforme (EM) is an acute immune-mediated inflammatory mucinous skin disorder. The etiology of pediatric EM involves infections, medications, autoimmune diseases, and genetic factors.Case Report: An 8-year-old girl with Mycopla
Externí odkaz:
https://doaj.org/article/7a5df348c9d04fc3a4caa38df263da87
Autor:
Hanbing Xia, Yanxia Yang, Xi Li, Jieluan Lu, Xiaomei Fan, Huijuan Guo, Qing Chen, Yuna Chen, Wenzhou Li
Publikováno v:
Frontiers in Neuroscience, Vol 15 (2021)
Frontiers in Neuroscience
Frontiers in Neuroscience
Epilepsy is a common neurologic disorder characterized by intractable seizures, involving genetic factors. There is a need to develop reliable genetic markers to predict the risk of epilepsy and design effective therapies. Arsenite methyltransferase
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd71c525e5d342af79631ce52a655ea2
https://doi.org/10.3389/fnins.2021.705297
https://doi.org/10.3389/fnins.2021.705297
Publikováno v:
Pharmacogenomics and Personalized Medicine
Jieluan Lu,1 Hanbing Xia,2 Wenzhou Li,2 Xianhuan Shen,1 Huijuan Guo,2 Jianping Zhang,1 Xiaomei Fan2 1Department of Clinical Pharmacology, College of Pharmacy, Jinan University, Guangzhou, 510632, Peopleâs Republic of China; 2Department of Pharma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b7006445365e673aa8fac3203fda2e7
https://www.dovepress.com/genetic-polymorphism-of-gabrg2-rs211037-is-associated-with-drug-respon-peer-reviewed-fulltext-article-PGPM
https://www.dovepress.com/genetic-polymorphism-of-gabrg2-rs211037-is-associated-with-drug-respon-peer-reviewed-fulltext-article-PGPM
Publikováno v:
Frontiers in Pediatrics
Frontiers in Pediatrics, Vol 9 (2021)
Frontiers in Pediatrics, Vol 9 (2021)
Background: Erythema multiforme (EM) is an acute immune-mediated inflammatory mucinous skin disorder. The etiology of pediatric EM involves infections, medications, autoimmune diseases, and genetic factors.Case Report: An 8-year-old girl with Mycopla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::980b2464c2cf494ee75b9023a7ff839e
http://europepmc.org/articles/PMC8358431
http://europepmc.org/articles/PMC8358431