Works by Wenping Xiong
Results: 20
Effects of heating coagulation of middle meningeal artery on plasma CGRP level and c-fos expression in migraine rat triggered by nitroglycerin.
- Published in:
- Neurological Sciences, 2011, v. 32, n. 4, p. 589, doi. 10.1007/s10072-011-0486-7
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- Article
Novel recessive PDZD7 biallelic mutations in two Chinese families with non-syndromic hearing loss.
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- American Journal of Medical Genetics. Part A, 2018, v. 176, n. 1, p. 99, doi. 10.1002/ajmg.a.38477
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- Article
Human adipose-derived mesenchymal stem cells repair cisplatin-induced acute kidney injury through antiapoptotic pathways.
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- Experimental & Therapeutic Medicine, 2015, v. 10, n. 2, p. 468, doi. 10.3892/etm.2015.2505
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- Article
Predicting intraoperative major blood loss in microsurgery for brain arteriovenous malformations.
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- Frontiers in Medicine, 2024, p. 1, doi. 10.3389/fmed.2024.1446088
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- Article
proBDNF expression induces apoptosis and inhibits synaptic regeneration by regulating the RhoA-JNK pathway in an in vitro post-stroke depression model.
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- Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01667-2
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- Article
Analysis of Clinical Effects of Comprehensive Nursing Based on Enhanced Recovery after Surgery in Patients with Embolization for Intracranial Aneurysms.
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- Computational & Mathematical Methods in Medicine, 2022, p. 1, doi. 10.1155/2022/3026680
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- Article
Flurbiprofen axetil protects against cerebral ischemia/reperfusion injury via regulating miR‐30c‐5p and SOX9.
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- Chemical Biology & Drug Design, 2022, v. 99, n. 2, p. 197, doi. 10.1111/cbdd.13973
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- Article
CircLPAR1 Promotes Neuroinflammation and Oxidative Stress in APP/PS1 Mice by Inhibiting SIRT1/Nrf-2/HO-1 Axis Through Destabilizing GDF-15 mRNA.
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- Molecular Neurobiology, 2023, v. 60, n. 4, p. 2236, doi. 10.1007/s12035-022-03177-8
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- Article
Rs12976445 polymorphism is associated with the risk of post-SAH re-bleeding by modulating the expression of microRNA-125 and ET-1.
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- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-021-04330-4
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- Article
Characteristics and prognostic analysis of simultaneous bilateral sudden sensorineural hearing loss.
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- Frontiers in Neurology, 2023, p. 1, doi. 10.3389/fneur.2023.1179579
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- Article
A novel dominant GJB2 (DFNA3) mutation in a Chinese family.
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- Scientific Reports, 2017, p. 34425, doi. 10.1038/srep34425
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- Article
Understanding auditory neuropathy spectrum disorder: a systematic review in transgenic mouse models.
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- SCIENCE CHINA Life Sciences, 2016, v. 59, n. 5, p. 480, doi. 10.1007/s11427-015-4985-2
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- Article
Impact of environmental noise exposure as an inducing factor on the prognosis of sudden sensorineural hearing loss: a retrospective case–control study.
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- Frontiers in Neuroscience, 2023, p. 1, doi. 10.3389/fnins.2023.1210291
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- Article
Idiopathic Sudden Sensorineural Hearing Loss in Different Ages: Prognosis of Patients With Initial Total Hearing Loss.
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- Frontiers in Psychology, 2022, v. 13, p. 1, doi. 10.3389/fpsyg.2022.818967
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- Article
Characteristics and prognosis analysis of bilateral sudden sensorineural hearing loss: A retrospective case–control study.
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- Clinical Otolaryngology, 2022, v. 47, n. 6, p. 732, doi. 10.1111/coa.13981
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- Article
Thromboelastography predicting the prognosis of sudden sensorineural hearing loss.
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- Clinical Otolaryngology, 2022, v. 47, n. 6, p. 724, doi. 10.1111/coa.13959
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- Article
Impact of hyperlipidemia as a coexisting factor on the prognosis of idiopathic sudden sensorineural hearing loss: A propensity score matching analysis.
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- Clinical Otolaryngology, 2020, v. 45, n. 1, p. 2, doi. 10.1111/coa.13421
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- Article
Analysis of Perioperative Nursing Intervention Effect of Cerebrovascular Intervention Patients Based on Intelligent Internet of Things.
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- BioMed Research International, 2022, v. 2022, p. 1, doi. 10.1155/2022/7800298
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- Article
Clinical value of auditory nerve enhancement in idiopathic sudden sensorineural hearing loss: a retrospective study.
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- Frontiers in Neurology, 2024, p. 1, doi. 10.3389/fneur.2024.1410516
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- Article
Targeted High-Throughput Sequencing Identifies Pathogenic Mutations in KCNQ4 in Two Large Chinese Families with Autosomal Dominant Hearing Loss.
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- PLoS ONE, 2014, v. 9, n. 8, p. 1, doi. 10.1371/journal.pone.0103133
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- Article