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Cited by in CrossRef
For: Al-Ani RM. Various aspects of hearing loss in newborns: A narrative review. World J Clin Pediatr 2023; 12(3): 86-96 [PMID: 37342452 DOI: 10.5409/wjcp.v12.i3.86]
URL: https://www.wjgnet.com/2219-2808/full/v12/i3/86.htm
Number Citing Articles
1
Xiaoli Tang, Xiaochen Yang, Jiajun Yuan, Jie Yang, Qian Jin, Hanting Zhang, Liebin Zhao, Weiwei Guo. Call for Decision Support for Electrocardiographic Alarm Administration Among Neonatal Intensive Care Unit Staff: Multicenter, Cross-Sectional SurveyJournal of Medical Internet Research 2024; 26: e60944 doi: 10.2196/60944
2
Justin Cottrell, Peter Dixon, Xingshan Cao, Alex Kiss, Kari Smilsky, Kassandra Kaminskas, Amy Ng, David Shipp, Andrew Dimitrijevic, Joseph Chen, Vincent Lin, Lianna Kyriakopoulou, Trung Le, Nejat Mahdieh. Gene mutations as a non-invasive measure of adult cochlear implant performance: Variable outcomes in patients with select TMPRSS3 mutationsPLOS ONE 2023; 18(9): e0291600 doi: 10.1371/journal.pone.0291600
3
Genevieve Choi, Holly Teagle, Suzanne Purdy, Andrew Wood. A treatment-focused approach to medical investigations for hearing loss in infantsJournal of the Royal Society of New Zealand 2024; : 1 doi: 10.1080/03036758.2024.2399340
4
Raid M. Al-Ani, Karrar Khalid Jamal, Fatima Wadhah Fakhri, Sabaa Haitham Muhamed, Nabaa Haitham Muhamed, Omar Fadhil Ali. Prevalence of hearing loss among patients attending the private otolaryngology clinic, Ramadi city, Anbar, IraqThe Egyptian Journal of Otolaryngology 2024; 40(1) doi: 10.1186/s43163-024-00636-y
5
Yixin Zhao, Yan Long, Tao Shi, Xin Ma, Chengyu Lian, Hanjun Wang, Hongen Xu, Lisheng Yu, Xiaotao Zhao. Validating the splicing effect of rare variants in the SLC26A4 gene using minigene assayBMC Medical Genomics 2024; 17(1) doi: 10.1186/s12920-024-02007-1