Shouyue Sun

发表

The Optimized Calculation Method for Insulin Dosage in an Insulin Tolerance Test (ITT): A Randomized Parallel Control Study

Weiqing Wang, G. Ning, Yuhong Chen, 2020, Frontiers in Endocrinology.

Genetic Findings in a Cohort of Patients with Androgen Insensitivity Syndrome

Yu Zhao, Weiqing Wang, L. Ye, 2021 .

A Novel SRD5A2 Mutation with Loss of Function Identified in Chinese Patients with Hypospadias

G. Ning, Hui-jie Zhang, Xiaoying Li, 2011, Hormone Research in Paediatrics.

New, recurrent, and prevalent mutations: Clinical and molecular characterization of 26 Chinese patients with 17alpha-hydroxylase/17,20-lyase deficiency

Weiqing Wang, Hui-jie Zhang, Xiaoying Li, 2015, The Journal of Steroid Biochemistry and Molecular Biology.

Untargeted LC/MS-Based Metabolic Phenotyping of Hypopituitarism in Young Males

Peizhan Chen, Yuwen Zhang, Fei Yuan, 2021, Frontiers in Pharmacology.

Clinical and molecular characterization of thirty Chinese patients with congenital lipoid adrenal hyperplasia

G. Ning, L. Ye, Junqi Wang, 2020, The Journal of Steroid Biochemistry and Molecular Biology.

17β-Hydroxysteroid dehydrogenase 3 deficiency: Three case reports and a systematic review

W. Wang, Yu Zhao, Weiqing Wang, 2017, The Journal of Steroid Biochemistry and Molecular Biology.

Sequential Versus Continual Purified Urinary FSH/hCG in Men With Idiopathic Hypogonadotropic Hypogonadism.

G. Ning, L. Shi, Zuojie Luo, 2015, The Journal of clinical endocrinology and metabolism.

Seven novel DAX1 mutations with loss of function identified in Chinese patients with congenital adrenal hypoplasia.

G. Ning, Y. Mu, Hui-jie Zhang, 2010, The Journal of clinical endocrinology and metabolism.

Targeted gene panel sequencing for molecular diagnosis of congenital adrenal hyperplasia

G. Ning, L. Ye, Yan Qi, 2021, The Journal of Steroid Biochemistry and Molecular Biology.

Surgical biopsies in patients with central diabetes insipidus and thickened pituitary stalks

Weiqing Wang, G. Ning, L. Bian, 2014, Endocrine.

Phenotype-genotype correlation in eight Chinese 17alpha-hydroxylase/17,20 lyase-deficiency patients with five novel mutations of CYP17A1 gene.

G. Ning, Y. Bi, Siyuan Zheng, 2006, The Journal of clinical endocrinology and metabolism.

Intensive insulin therapy combined with metformin is associated with reduction in both glucose variability and nocturnal hypoglycaemia in patients with type 2 diabetes

Weiqing Wang, G. Ning, Zhiyun Zhao, 2017, Diabetes/metabolism research and reviews.

A prevalent and three novel mutations in CYP11B1 gene identified in Chinese patients with 11-beta hydroxylase deficiency

Weiqing Wang, G. Ning, Hui-jie Zhang, 2013, The Journal of Steroid Biochemistry and Molecular Biology.

Diabetic Ketoacidosis at Diagnosis Influences Complete Remission After Treatment With Hematopoietic Stem Cell Transplantation in Adolescents With Type 1 Diabetes

Weiqing Wang, G. Ning, Jiong Hu, 2012, Diabetes Care.

Nonclassic Adrenal Hyperplasia (NCAH) due to 21-hydroxylase deficiency: A cohort of 78 patients

Weiqing Wang, L. Ye, Xiaoyan Xie, 2022, The Journal of Steroid Biochemistry and Molecular Biology.

Six cases of ectopic ACTH syndrome caused by thymic carcinoid

Weiqing Wang, Y. Bi, L. Ye, 2006, Journal of endocrinological investigation.

COVID-19 Rebound After VV116 vs Nirmatrelvir-Ritonavir Treatment

R. Zheng, Yu Xu, Mian Li, 2024, JAMA network open.