Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Wenjia Dai"'
Autor:
Chengbei Bao, Yan Zhao, Renwei Luo, Qiuyun Xu, Zequn Tong, Zhixun Xiao, Zheyu Zhuang, Wenjia Dai, Bohan Gu, Ting Gong, Bo Cheng, Chao Ji
Publikováno v:
Dermatology and Therapy, Vol 13, Iss 12, Pp 3071-3084 (2023)
Abstract Introduction The treatment of genital lichen sclerosus (GLS) remains challenging. Baricitinib has been introduced in the treatment of GLS, but there’s no imaging evaluation for GLS patients treated with it. No comparison of dermoscopy and
Externí odkaz:
https://doaj.org/article/1a1acd989a544cd882c097ae7a6ca580
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 134:110058
Introduction Otitis media with effusion (OME) is one of the most common pediatric diseases worldwide. Several studies have analyzed the diversity of the microbiomes found in the middle ear effusions (MEEs) of populations from developed countries. How
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00962ecc5bd2cdc65d3c1dbf43aec732
https://doi.org/10.1016/j.ijporl.2020.110058
https://doi.org/10.1016/j.ijporl.2020.110058
Publikováno v:
Polymer Bulletin. 66:703-710
In the present study, attempts have been made to modify a phenolic resin (PF) with vinyl triethoxysilane (VTES) in order to compatibilize it with EPDM. It was proved by Fourier transform infrared spectrometer (FTIR) that vinyl-silicon group had been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76e91e59bf0c2bd0a51f5e9f8cdd1db8
https://doi.org/10.1007/s00289-010-0374-y
https://doi.org/10.1007/s00289-010-0374-y
Publikováno v:
Genetic testing and molecular biomarkers. 15(5)
To explore possible correlations between the genotype of GJB2, the gene that encodes connexin 26 (Cx26), and its related audiogram features in Chinese patients with less severe nonsyndromic hearing loss (HL), we examined the pure tone audiograms and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e07fa0bfce55c6e504cda18d41e7fe96
https://pubmed.ncbi.nlm.nih.gov/21366436
https://pubmed.ncbi.nlm.nih.gov/21366436
Autor:
Yan Bai, Zhengmin Wang, Wenjia Dai, Qingzhong Li, Guoling Chen, Ning Cong, Minxin Guan, Huawei Li
Publikováno v:
BMC Medical Genetics; 2010, Vol. 11, p129-139, 11p
Autor:
Min-Xin Guan, Guoling Chen, Ning Cong, Zhengmin Wang, Huawei Li, Wenjia Dai, Yan Bai, Qingzhong Li
Publikováno v:
BMC Medical Genetics
BMC Medical Genetics, Vol 11, Iss 1, p 129 (2010)
BMC Medical Genetics, Vol 11, Iss 1, p 129 (2010)
Background The 1555A > G mutation is the most common cause of aminoglycoside-induced and non-syndromic deafness. However, the variable clinical phenotype and incomplete penetrance of A1555G-induced hearing loss complicate our understanding of this mu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1de3d317133edbc72f0919f84d252961