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Frontiers in Medicine|June 28, 2021
Urinary Extracellular Vesicles for Renal Tubular Transporters Expression in Patients With Gitelman SyndromeChih-Chien Sung, Min-Hsiu Chen, Yi-Chang Lin, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|August 28, 2018
Generation and analysis of a mouse model of pseudohypoaldosteronism type II caused by KLHL3 mutation in BTB domainChien-Ming Lin, Chih-Jen Cheng, Sung-Sen Yang, et al.
Frontiers in Genetics|July 18, 2022
Novel CNNM2 Mutation Responsible for Autosomal-Dominant Hypomagnesemia With SeizureMin-Hua Tseng, Sung-Sen Yang, Chih-Chien Sung, et al.
The American Journal of the Medical Sciences|August 16, 2011
Genotype and phenotype analysis of patients with sporadic periodic paralysisChih-Chien Sung, Chih-Jen Cheng, Yi-Fen Lo, et al.
European Journal of Endocrinology|August 14, 2013
A 10-year analysis of thyrotoxic periodic paralysis in 135 patients: focus on symptomatology and precipitantsChin-Chun Chang, Chih-Jen Cheng, Chih-Chien Sung, et al.
Molecular Cancer|February 22, 2014
WNK1-OSR1 kinase-mediated phospho-activation of Na+-K+-2Cl- cotransporter facilitates glioma migrationWen Zhu, Gulnaz Begum, Kelli Pointer, et al.
Mayo Clinic Proceedings|January 26, 2005
Thyrotoxic periodic paralysisShih-Hua Lin
NPJ Genomic Medicine|August 14, 2021
Allele-specific RT-PCR for the rapid detection of recurrent SLC12A3 mutations for Gitelman syndromeMing-Tso Yan, Sung-Sen Yang, Min-Hua Tseng, et al.
The Journal of Clinical Endocrinology and Metabolism|June 9, 2012
Genotype, phenotype, and follow-up in Taiwanese patients with salt-losing tubulopathy associated with SLC12A3 mutationMin-Hua Tseng, Sung-Sen Yang, Yu-Juei Hsu, et al.
European Journal of Endocrinology|September 17, 2009
Therapeutic analysis in Chinese patients with thyrotoxic periodic paralysis over 6 yearsJeng-Chuan Shiang, Chih-Jen Cheng, Ming-Kai Tsai, et al.
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