| For: | You JY, Xiong LY, Wu MF, Fan JS, Fu QH, Qiu MH. Genetic variation features of neonatal hyperbilirubinemia caused by inherited diseases. World J Clin Pediatr 2024; 13(4): 98462 [PMID: 39654666 DOI: 10.5409/wjcp.v13.i4.98462] |
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| URL: | https://www.wjgnet.com/2219-2808/full/v13/i4/98462.htm |
| Number | Citing Articles |
| 1 |
Shu-Mei Pan, Wen-Cai Liu, Chun-Yu Xing, Xin-Yue Pu, Qian-Qian Wang, Xuan Zhao, Qi-Chen Zhang, Dan-Dan Wang, Ya-di Zhu. Corylin induces UGT1A1 via PPARs/AhR and exerts hepatoprotection in mice. Bioorganic & Medicinal Chemistry 2025; 131 doi: 10.1016/j.bmc.2025.118433
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| 2 |
Darren L. Pereira, Ataah S. Qureshi. A rare case of Crigler–Najjar syndrome type II in a preterm infant: clinical, genetic and therapeutic insights into the UGT1A1 Pro176Leu variant. International Journal of Contemporary Pediatrics 2026; 13(6) doi: 10.18203/2349-3291.ijcp20261552
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