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Yi-Ming Mu

Showing results (81-90 of 93) with videos related to

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World Journal of Clinical Cases|May 24, 2019
Bilateral adrenocortical adenomas causing adrenocorticotropic hormone-independent Cushing's syndrome: A case report and review of the literatureYu-Lin Gu, Wei-Jun Gu, Jing-Tao Dou, et al.
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. Acta Academiae Medicinae Sinicae|November 10, 2016
Clinical Features of Pituitary Stalk Interruption Syndrome in 114 CasesBai-Yu Han, Qian Zhang, Le-Le Li, et al.
Endocrine Journal|September 11, 2013
Female sex hormones are associated with the reduction of serum sodium and hypertension complications in patients with aldosterone-producing adenomaZhao-Hui Lu, Xiao-Xiao Zhu, Zhi-qing Tang, et al.
Zhonghua Nei Ke Za Zhi|February 8, 2014
[The clinical characteristics of multi-detector computed tomography of congenital adrenal hyperplasia]Wei-jun Gu, Xiao-yan Wang, Jing-tao Dou, et al.
Medicine|May 29, 2015
Characterization of papillary thyroid microcarcinomas using sonographic features in malignant papillary thyroid cancer: a retrospective analysisWei-Jun Gu, Hui-Xian Yan, Yu-Kun Luo, et al.
Annals of Hepatology|August 14, 2022
Randomised controlled trial: effect of metformin add-on therapy on functional cure in entecavir-treated patients with chronic hepatitis BWei Zhang, Yuan-Yuan Li, Qing-Hua Shang, et al.
Chinese Medical Journal|March 22, 2016
Initiating Characteristics of Early-onset Type 2 Diabetes Mellitus in Chinese PatientsHui Yu, Li-Fang Xie, Kang Chen, et al.
Medicine|February 27, 2018
Thyrotrophic status in patients with pituitary stalk interruption syndromeQian Zhang, Li Zang, Yi-Jun Li, et al.
Endocrine Journal|December 28, 2017
Whole-genome sequencing revealed armadillo repeat containing 5 (ARMC5) mutation in a Chinese family with ACTH-independent macronodular adrenal hyperplasiaQian Zhang, Liang Cui, Jiang-Ping Gao, et al.
Experimental Biology and Medicine (Maywood, N.J.)|June 3, 2015
Mutation analyses in pedigrees and sporadic cases of ethnic Han Chinese Kallmann syndrome patientsWei-Jun Gu, Qian Zhang, Ying-Qian Wang, et al.
Pageof 10

Showing results (81-90 of 93) with videos related to

Sort By:
Pageof 10
World Journal of Clinical Cases|May 24, 2019
Bilateral adrenocortical adenomas causing adrenocorticotropic hormone-independent Cushing's syndrome: A case report and review of the literatureYu-Lin Gu, Wei-Jun Gu, Jing-Tao Dou, et al.
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. Acta Academiae Medicinae Sinicae|November 10, 2016
Clinical Features of Pituitary Stalk Interruption Syndrome in 114 CasesBai-Yu Han, Qian Zhang, Le-Le Li, et al.
Endocrine Journal|September 11, 2013
Female sex hormones are associated with the reduction of serum sodium and hypertension complications in patients with aldosterone-producing adenomaZhao-Hui Lu, Xiao-Xiao Zhu, Zhi-qing Tang, et al.
Zhonghua Nei Ke Za Zhi|February 8, 2014
[The clinical characteristics of multi-detector computed tomography of congenital adrenal hyperplasia]Wei-jun Gu, Xiao-yan Wang, Jing-tao Dou, et al.
Medicine|May 29, 2015
Characterization of papillary thyroid microcarcinomas using sonographic features in malignant papillary thyroid cancer: a retrospective analysisWei-Jun Gu, Hui-Xian Yan, Yu-Kun Luo, et al.
Annals of Hepatology|August 14, 2022
Randomised controlled trial: effect of metformin add-on therapy on functional cure in entecavir-treated patients with chronic hepatitis BWei Zhang, Yuan-Yuan Li, Qing-Hua Shang, et al.
Chinese Medical Journal|March 22, 2016
Initiating Characteristics of Early-onset Type 2 Diabetes Mellitus in Chinese PatientsHui Yu, Li-Fang Xie, Kang Chen, et al.
Medicine|February 27, 2018
Thyrotrophic status in patients with pituitary stalk interruption syndromeQian Zhang, Li Zang, Yi-Jun Li, et al.
Endocrine Journal|December 28, 2017
Whole-genome sequencing revealed armadillo repeat containing 5 (ARMC5) mutation in a Chinese family with ACTH-independent macronodular adrenal hyperplasiaQian Zhang, Liang Cui, Jiang-Ping Gao, et al.
Experimental Biology and Medicine (Maywood, N.J.)|June 3, 2015
Mutation analyses in pedigrees and sporadic cases of ethnic Han Chinese Kallmann syndrome patientsWei-Jun Gu, Qian Zhang, Ying-Qian Wang, et al.
Pageof 10