Drug response is related to NR3C1 and FAAH polymorphism in Chinese pediatric epilepsy patients
Abstract Background Childhood epilepsy is a common neurological syndrome with complex etiology and recurrent seizures. It seriously affects the growth and development of child patients. Methods NR3C1 rs41423247 and FAAH rs324420 polymorphisms were detected by the polymerase chain reaction in 105 ped...
Saved in:
Main Authors: | Hongli Wang, Chu Li, Qian Li, Ning Li, Huiling Qin |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2025-02-01
|
Series: | Italian Journal of Pediatrics |
Subjects: | |
Online Access: | https://doi.org/10.1186/s13052-025-01870-7 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Anticonvulsant Effects of Synthetic <i>N</i>-(3-Methoxybenzyl)oleamide and <i>N</i>-(3-Methoxybenzyl)linoleamide Macamides: An In Silico and In Vivo Study
by: Karin Jannet Vera-López, et al.
Published: (2025-01-01) -
Evaluating the Association Between Methylenetetrahydrofolate Reductase (Rs1801131 and Rs1801133) Gene Polymorphisms and Severity of Coronary Lesions in Patients With STEMI and NSTEMI: A Retrospective Cross‐Sectional Study
by: Behnam Nazarzadeh, et al.
Published: (2025-01-01) -
The Role of Ubiquitin-Like Interferon (IFN)-Stimulated 15 and IFN Gamma Genes Polymorphism with the Severity and Serum Biochemical Markers in COVID-19 Patients
by: Khadijah Gatfan Hosseien, et al.
Published: (2024-12-01) -
Frequency of IL-1B Gene Polymorphisms in Patients with Gastroesophageal Cancer in the Hakkari Region
by: Derya Yaman, et al.
Published: (2024-01-01) -
Association of rs3755319 and rs4148325 of the <i>UGT1A1</i> gene, rs2328136 of the <i>NUP153-AS</i> gene, and rs16928809 of the <i>SLC22A18</i> gene with benign unconjugated hyperbilirubinemia
by: Anastasiya A. Ivanova, et al.
Published: (2024-12-01)