臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

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Showing items 291-300 of 2057 (206 Page(s) Totally)
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Institution	Date	Title	Author
臺大學術典藏	2021-07-06T02:37:31Z	Prognostic effect of high-density lipoprotein cholesterol level in patients with atherosclerotic cardiovascular disease under statin treatment	Li Y.-H.; Tseng W.-K.; Yin W.-H.; FANG-JU LIN; Wu Y.-W.; Hsieh I.-C.; Lin T.-H.; Sheu W.H.-H.; Yeh H.-I.; Chen J.-W.; Wu C.-C.; Taiwanese Secondary Prevention for Patients with AtheRosCLErotic Disease (T-SPARCLE) Registry Investigators
臺大學術典藏	2021-07-06T02:37:31Z	Clinical pharmacy service and international collaboration: Model and experience from a medical center in Taiwan	Wu C.-C.; FANG-JU LIN; Lin S.-W.; Ho Y.-F.; Huang C.-F.; Shen L.-J.; Wu F.-L.L.
臺大學術典藏	2021-07-06T02:37:30Z	Comparison of risk of acute kidney injury between patients receiving the combination of teicoplanin and piperacillin/tazobactam versus vancomycin and piperacillin/tazobactam	Shao C.-H.; Tai C.-H.; FANG-JU LIN; Wu C.-C.; Wang J.-T.; Wang C.-C.
臺大學術典藏	2021-07-06T02:37:29Z	Nephrotoxicity of teicoplanin-based combination therapy: Focus on piperacillin/tazobactam and other anti-pseudomonal β-lactams	Tai C.-H.; Shao C.-H.; Wang C.-C.; FANG-JU LIN; Wang J.-T.; Wu C.-C.
臺大學術典藏	2021-07-06T02:04:15Z	Application of Massively Parallel Sequencing to Genetic Diagnosis in Multiplex Families with Idiopathic Sensorineural Hearing Impairment	Wu C.-C.; Lin Y.-H.; Lu Y.-C.; Chen P.-J.; Yang W.-S.; Hsu C.-J.; PEI-LUNG CHEN
臺大學術典藏	2021-07-06T02:04:15Z	Common genetic mutations in the start codon of the SDH subunit D gene among Chinese families with familial head and neck paragangliomas	Wang C.-P.; Chen T.-C.; Chang Y.-L.; Ko J.-Y.; Yang T.-L.; Lo F.-Y.; Hu Y.-L.; PEI-LUNG CHEN; Wu C.-C.; Lou P.-J.
臺大學術典藏	2021-07-06T02:04:11Z	Identification of a novel GATA3 mutation in a deaf Taiwanese family by massively parallel sequencing	Lin Y.-H.; Wu C.-C.; Hsu T.-Y.; Chiu W.-Y.; Hsu C.-J.; PEI-LUNG CHEN
臺大學術典藏	2021-07-06T02:04:09Z	Identifying children with poor cochlear implantation outcomes using massively parallel sequencing	Wu C.-C.; Lin Y.-H.; Liu T.-C.; Lin K.-N.; Yang W.-S.; Hsu C.-J.; PEI-LUNG CHEN; Wu C.-M.
臺大學術典藏	2021-07-06T02:04:07Z	Long-term cochlear implant outcomes in children with GJB2 and SLC26A4 mutations	Wu C.-M.; Ko H.-C.; Tsou Y.-T.; Lin Y.-H.; Lin J.-L.; Chen C.-K.; PEI-LUNG CHEN; Wu C.-C.
臺大學術典藏	2021-07-06T02:04:02Z	A novel missense variant in the nuclear localization signal of POU4F3 causes autosomal dominant non-syndromic hearing loss	Lin Y.-H.; Lin Y.-H.; Lu Y.-C.; Liu T.-C.; Chen C.-Y.; Hsu C.-J.; PEI-LUNG CHEN; Wu C.-C.

Showing items 291-300 of 2057 (206 Page(s) Totally)
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View [10|25|50] records per page