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Shang Yi

Showing results (161-170 of 357) with videos related to

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Journal of Microbiology, Immunology, and Infection = Wei Mian Yu Gan Ran Za Zhi|October 19, 2019
Ambulatory independence is associated with higher incidence of latent tuberculosis infection in long-term care facilities in TaiwanShang-Yi Lin, Jung-Yien Chien, Hsiu-Tzy Chiang, et al.
Journal of Microbiology, Immunology, and Infection = Wei Mian Yu Gan Ran Za Zhi|June 17, 2018
Three months of rifapentine and isoniazid for latent tuberculosis infection in hemodialysis patients: High rates of adverse eventsShang-Yi Lin, Yi-Wen Chiu, Po-Liang Lu, et al.
Respirology (Carlton, Vic.)|June 27, 2018
Metformin is associated with a lower risk of active tuberculosis in patients with type 2 diabetesShang-Yi Lin, Hung-Pin Tu, Po-Liang Lu, et al.
Journal of Clinical Microbiology|May 12, 2025
<i>In vitro</i> activity of isavuconazole, ravuconazole, and comparison of the Sensititre YeastOne and CLSI broth microdilution methods against clinical isolates of <i>Trichosporon</i> speciesShih-Hao Lo, Yi-Ting Tseng, Yee-Chun Chen, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 31, 2022
Novel SLC12A1 mutations cause Bartter syndrome in two patients with different prognosesSheng Yi, Mengting Li, Qi Yang, et al.
Neurology. Genetics|October 24, 2022
Novel Synonymous and Frameshift Variants in the <i>TRIP12</i> Gene Identified in 2 Chinese Patients With Intellectual DisabilitySheng Yi, Fei Chen, Zailong Qin, et al.
Heliyon|March 18, 2024
A nonsense <i>CC2D1A</i> variant is associated with congenital anomalies, motor delay, hypotonia, and slight deformitiesSheng Yi, Xianglian Tang, Qiang Zhang, et al.
Hemoglobin|November 23, 2017
Characterization of a Large Novel α-Globin Gene Cluster Deletion Causing α<sup>0</sup>-Thalassemia in a Chinese FamilySheng He, Qian Qin, Peng Huang, et al.
BMC Medical Genetics|May 13, 2020
A novel pathogenic frameshift variant unmasked by a large de novo deletion at 13q21.33-q31.1 in a Chinese patient with neuronal ceroid lipofuscinosis type 5Wei Li, Xin Fan, Yue Zhang, et al.
Frontiers in Pediatrics|October 4, 2024
Novel loss-of-function variants in <i>WDR26</i> cause Skraban-Deardorff syndrome in two Chinese patientsQi Yang, Xunzhao Zhou, Sheng Yi, et al.
Pageof 36

Showing results (161-170 of 357) with videos related to

Sort By:
Pageof 36
Journal of Microbiology, Immunology, and Infection = Wei Mian Yu Gan Ran Za Zhi|October 19, 2019
Ambulatory independence is associated with higher incidence of latent tuberculosis infection in long-term care facilities in TaiwanShang-Yi Lin, Jung-Yien Chien, Hsiu-Tzy Chiang, et al.
Journal of Microbiology, Immunology, and Infection = Wei Mian Yu Gan Ran Za Zhi|June 17, 2018
Three months of rifapentine and isoniazid for latent tuberculosis infection in hemodialysis patients: High rates of adverse eventsShang-Yi Lin, Yi-Wen Chiu, Po-Liang Lu, et al.
Respirology (Carlton, Vic.)|June 27, 2018
Metformin is associated with a lower risk of active tuberculosis in patients with type 2 diabetesShang-Yi Lin, Hung-Pin Tu, Po-Liang Lu, et al.
Journal of Clinical Microbiology|May 12, 2025
<i>In vitro</i> activity of isavuconazole, ravuconazole, and comparison of the Sensititre YeastOne and CLSI broth microdilution methods against clinical isolates of <i>Trichosporon</i> speciesShih-Hao Lo, Yi-Ting Tseng, Yee-Chun Chen, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 31, 2022
Novel SLC12A1 mutations cause Bartter syndrome in two patients with different prognosesSheng Yi, Mengting Li, Qi Yang, et al.
Neurology. Genetics|October 24, 2022
Novel Synonymous and Frameshift Variants in the <i>TRIP12</i> Gene Identified in 2 Chinese Patients With Intellectual DisabilitySheng Yi, Fei Chen, Zailong Qin, et al.
Heliyon|March 18, 2024
A nonsense <i>CC2D1A</i> variant is associated with congenital anomalies, motor delay, hypotonia, and slight deformitiesSheng Yi, Xianglian Tang, Qiang Zhang, et al.
Hemoglobin|November 23, 2017
Characterization of a Large Novel α-Globin Gene Cluster Deletion Causing α<sup>0</sup>-Thalassemia in a Chinese FamilySheng He, Qian Qin, Peng Huang, et al.
BMC Medical Genetics|May 13, 2020
A novel pathogenic frameshift variant unmasked by a large de novo deletion at 13q21.33-q31.1 in a Chinese patient with neuronal ceroid lipofuscinosis type 5Wei Li, Xin Fan, Yue Zhang, et al.
Frontiers in Pediatrics|October 4, 2024
Novel loss-of-function variants in <i>WDR26</i> cause Skraban-Deardorff syndrome in two Chinese patientsQi Yang, Xunzhao Zhou, Sheng Yi, et al.
Pageof 36