Jing Cheng

发表

Clinical features and mutational analysis in 114 young children with Wilson disease from South China

Yunting Lin, Hongsheng Liu, Yonglan Huang, 2019, American journal of medical genetics. Part A.

Phenotype and molecular characteristics in 45 Chinese children with 5α‐reductase type 2 deficiency from South China

Guochang Liu, Li Liu, H. Sheng, 2015, Clinical endocrinology.

Clinical Management and Gene Mutation Analysis of Children with Congenital Hyperinsulinism in South China

Yunting Lin, Z. Wen, C. Zeng, 2019, Journal of clinical research in pediatric endocrinology.

Glucose-6-Phosphate dehydrogenase deficiency associated hemolysis in a cohort of new onset type 1 diabetes children in Guangdong province, China

Yunting Lin, Li Liu, Xiuzhen Li, 2022, Diabetology & Metabolic Syndrome.

Phenotypic and Molecular Characteristics of Children with Progressive Familial Intrahepatic Cholestasis in South China

Wen Zhang, Li Liu, Yan-na Cai, 2020, Pediatric gastroenterology, hepatology & nutrition.

A compound heterozygous mutation of ABCC8 gene causing a diazoxide-unresponsive congenital hyperinsulinism with an atypical form: Not a focal lesion in the pancreas reported by ¹⁸F-DOPA-PET/CT scan.

Fenghua Wang, Hongsheng Liu, Z. Wen, 2015, Gene.

Chemoprevention of Lung Carcinogenesis by Red Ginseng and Ginsenoside Rg3 in A/J mice

M. You, Yian Wang, Shengli Yang, 2020 .

Interleukin-10 gene transfer into insulin-producing β cells protects against diabetes in non-obese diabetic mice.

Wei Zhu, Li Liu, Xiuzhen Li, 2015, Molecular medicine reports.

A novel ABCD1 gene mutation in a Chinese patient with X-linked adrenoleukodystrophy

Li Liu, Li-ping Fan, Yan-na Cai, 2015, Journal of pediatric endocrinology & metabolism : JPEM.

Clinical and molecular characteristics of patients with Gaucher disease in Southern China.

Yuyu Feng, Hao Hu, T. Xie, 2018, Blood cells, molecules & diseases.

[Clinical features and StAR gene mutations in children with congenital lipoid adrenal hyperplasia].

T. Xie, Li Liu, Dongyan Wu, 2015, Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics.

Clinical presentation and mutational spectrum in a series of 166 patients with classical 21-hydroxylase deficiency from South China.

Zhichun Feng, Li Liu, Yan-na Cai, 2018, Clinica chimica acta; international journal of clinical chemistry.

Molecular diagnosis of maturity‐onset diabetes of the young in a cohort of Chinese children

Yunting Lin, C. Zeng, Li Liu, 2020, Pediatric diabetes.

Clinical characteristics and long-term outcomes of 12 children with vitamin D-dependent rickets type 1A: A retrospective study

Wen Zhang, Yunting Lin, C. Zeng, 2022, Frontiers in Pediatrics.

Molecular and clinical characteristics of monogenic diabetes mellitus in southern Chinese children with onset before 3 years of age

Yunting Lin, C. Zeng, Li Liu, 2020, BMJ open diabetes research & care.

Detection of inborn errors of metabolism using GC-MS: over 3 years of experience in southern China

Li Liu, Yan-na Cai, Xiuzhen Li, 2015, Journal of pediatric endocrinology & metabolism : JPEM.

Early transition from insulin to sulfonylureas in neonatal diabetes and follow‐up: Experience from China

Li Liu, Xinjiang Huang, H. Sheng, 2018, Pediatric diabetes.

[Kniest dysplasia due to mutation of COL2A1 gene].

Hongsheng Liu, Yonglan Huang, Li Liu, 2015, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Features of BSCL2 related congenital generalized lipodystrophy in China: long-term follow-up of three patients and literature review

Wen Zhang, Yunting Lin, C. Zeng, 2022, Journal of pediatric endocrinology & metabolism : JPEM.

Somatic and germline FOXP3 mosaicism in the mother of a boy with IPEX syndrome

Yunting Lin, C. Zeng, Li Liu, 2018, European journal of immunology.

Clinical Management and Gene Mutation Analysis of Children with Congenital Hyperinsulinism in South China

Yunting Lin, Z. Wen, C. Zeng, 2019, Journal of clinical research in pediatric endocrinology.

Interleukin-10 gene transfer into insulin-producing β cells protects against diabetes in non-obese diabetic mice.

Wei Zhu, Li Liu, Xiuzhen Li, 2015, Molecular medicine reports.

Clinical and genetic analysis of methylmalonic aciduria in 60 patients from Southern China: a single center retrospective study

Yunting Lin, Yonglan Huang, Yan-na Cai, 2024, Orphanet journal of rare diseases.

Clinical and molecular characteristics in 15 patients with androgen receptor gene mutations from South China

G. Liu, Yan-na Cai, H. Sheng, 2017, Andrologia.