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PubPharm (75)
1
Shikonin potentiates skin wound healing in Sprague-Dawley rats by stimulating fibroblast and endothelial cell proliferation and angiogenesis
enthalten in:
The journal of gene medicine
| 2024
von
Xue, C.
|
Dou, J.
|
Zhang, S.
| +2
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2
Formononetin ameliorates cisplatin-induced hair cell death via activation of the PI3K/AKT-Nrf2 signaling pathway
enthalten in:
Heliyon
| 2024
von
Li, Y.
|
Wu, J.
|
Yu, H.
| +2
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3
Shikonin potentiates skin wound healing in Sprague–Dawley rats by stimulating fibroblast and endothelial cell proliferation and angiogenesis
enthalten in:
The Journal of Gene Medicine
| 2024
von
Xue, C.
|
Dou, J.
|
Zhang, S.
| +2
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4
Association between severe preoperative hearing impairment and postoperative emergence agitation among elderly patients undergoing middle ear surgery
enthalten in:
Journal of clinical anesthesia
| 2023
von
Shen, X.
|
Yu, H.
|
Chen, K.
| +3
CommentIn: J Clin Anesth. 2024 Jun;94:111394. - PMID 38237441
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5
Prognosis of vestibular dysfunction in idiopathic sudden sensorineural hearing loss with vertigo : a prospective cohort study
enthalten in:
Journal of neurology
| 2023
von
Hao, W.
|
Ye, L.
|
Yu, H.
| +1
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6
Prognosis of vestibular dysfunction in idiopathic sudden sensorineural hearing loss with vertigo: a prospective cohort study
enthalten in:
Journal of neurology
| 2023
von
Hao, W.
|
Ye, L.
|
Yu, H.
| +1
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7
The clinical effects of modified tinnitus relieving sound (MTRS) for chronic tinnitus : protocol for a randomized controlled trial
enthalten in:
Trials
| 2023
von
Tang, D.
|
Wang, J.
|
Yu, X.
| +1
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8
The clinical effects of modified tinnitus relieving sound (MTRS) for chronic tinnitus: protocol for a randomized controlled trial
enthalten in:
Trials
| 2023
von
Tang, D.
|
Wang, J.
|
Yu, X.
| +1
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9
A novel frameshift variant of LMX1A that leads to autosomal dominant non-syndromic sensorineural hearing loss : functional characterization of the C-terminal domain in LMX1A
enthalten in:
Human molecular genetics
| 2023
von
Xiao, M.
|
Zheng, Y.
|
Huang, K.
| +7
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10
Novel cis compound heterozygous variants in MYO6 causes early onset of non-syndromic hearing loss in a Chinese family
enthalten in:
Frontiers in genetics
| 2023
von
Ji, H.
|
Zhang, L.
|
Hussain, H.
| +3
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