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Zhaolin Lu

Showing results (41-50 of 55) with videos related to

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Endocrine|November 3, 2017
Efficacy of dexamethasone suppression test during the diagnosis of primary pigmented nodular adrenocortical disease in Chinese adrenocorticotropic hormone-independent Cushing syndromeShi Chen, Ran Li, Lin Lu, et al.
Frontiers in Endocrinology|September 20, 2021
An Optimized Pathway for the Differential Diagnosis of ACTH-Dependent Cushing's Syndrome Based on Low-Dose Dexamethasone Suppression TestKang Chen, Shi Chen, Lin Lu, et al.
Ophthalmology and Therapy|March 4, 2023
3D Visualization System-Assisted Vitrectomy for Rhegmatogenous Retinal Detachment: Leave Out the Perfluorocarbon LiquidLina Guan, Jiayu Chen, Yu Tang, et al.
Human Genetics|March 26, 2009
Novel human pathological mutations. Gene symbol: NR0B1. Disease: adrenal hypoplasiaMin Nie, Yong Fu, Lin Lu, et al.
The Journal of Clinical Endocrinology and Metabolism|November 24, 2019
The Optimal Cut-off of BIPSS in Differential Diagnosis of ACTH-dependent Cushing's Syndrome: Is Stimulation Necessary?Shi Chen, Kang Chen, Shirui Wang, et al.
Calcified Tissue International|October 9, 2023
Bone Microarchitecture and Volumetric Mineral Density Assessed by HR-pQCT in Patients with 21- and 17α-Hydroxylase DeficiencyXu Sun, Yijun Wu, Lin Lu, et al.
Behavioral Sciences (Basel, Switzerland)|June 26, 2026
A Double-Edged Algorithm Attitude: How Appreciation and Aversion Shape Students' AI Learning Anxiety in Higher EducationZhaolin Lu, Jiayuan Guo, Tian Yuan, et al.
Human Genetics|March 26, 2009
Novel human pathological mutations. Gene symbol: NROB1. Disease: adrenal hypoplasiaMin Nie, Yong Fu, Lin Lu, et al.
Human Genetics|March 26, 2009
Novel human pathological mutations. Gene symbol: NROB1. Disease: adrenal hypoplasiaMin Nie, Yong Fu, Lin Lu, et al.
Steroids|July 15, 2019
Analysis of novel heterozygous mutations in the CYP11B2 gene causing congenital aldosterone synthase deficiency and literature reviewHui Miao, Zhongxun Yu, Lin Lu, et al.
Pageof 6

Showing results (41-50 of 55) with videos related to

Sort By:
Pageof 6
Endocrine|November 3, 2017
Efficacy of dexamethasone suppression test during the diagnosis of primary pigmented nodular adrenocortical disease in Chinese adrenocorticotropic hormone-independent Cushing syndromeShi Chen, Ran Li, Lin Lu, et al.
Frontiers in Endocrinology|September 20, 2021
An Optimized Pathway for the Differential Diagnosis of ACTH-Dependent Cushing's Syndrome Based on Low-Dose Dexamethasone Suppression TestKang Chen, Shi Chen, Lin Lu, et al.
Ophthalmology and Therapy|March 4, 2023
3D Visualization System-Assisted Vitrectomy for Rhegmatogenous Retinal Detachment: Leave Out the Perfluorocarbon LiquidLina Guan, Jiayu Chen, Yu Tang, et al.
Human Genetics|March 26, 2009
Novel human pathological mutations. Gene symbol: NR0B1. Disease: adrenal hypoplasiaMin Nie, Yong Fu, Lin Lu, et al.
The Journal of Clinical Endocrinology and Metabolism|November 24, 2019
The Optimal Cut-off of BIPSS in Differential Diagnosis of ACTH-dependent Cushing's Syndrome: Is Stimulation Necessary?Shi Chen, Kang Chen, Shirui Wang, et al.
Calcified Tissue International|October 9, 2023
Bone Microarchitecture and Volumetric Mineral Density Assessed by HR-pQCT in Patients with 21- and 17α-Hydroxylase DeficiencyXu Sun, Yijun Wu, Lin Lu, et al.
Behavioral Sciences (Basel, Switzerland)|June 26, 2026
A Double-Edged Algorithm Attitude: How Appreciation and Aversion Shape Students' AI Learning Anxiety in Higher EducationZhaolin Lu, Jiayuan Guo, Tian Yuan, et al.
Human Genetics|March 26, 2009
Novel human pathological mutations. Gene symbol: NROB1. Disease: adrenal hypoplasiaMin Nie, Yong Fu, Lin Lu, et al.
Human Genetics|March 26, 2009
Novel human pathological mutations. Gene symbol: NROB1. Disease: adrenal hypoplasiaMin Nie, Yong Fu, Lin Lu, et al.
Steroids|July 15, 2019
Analysis of novel heterozygous mutations in the CYP11B2 gene causing congenital aldosterone synthase deficiency and literature reviewHui Miao, Zhongxun Yu, Lin Lu, et al.
Pageof 6