Zhu-hui Zhao

发表

Rapidly rising incidence of childhood type 1 diabetes in Chinese population: epidemiology in Shanghai during 1997–2011

Xuefan Gu, Xiaodong Wang, Chengjun Sun, 2014, Acta Diabetologica.

Relationship between initial treatment effect of recombinant human growth hormone and exon 3 polymorphism of growth hormone receptor in Chinese children with growth hormone deficiency.

F. Luo, Lingfeng Cao, Li Xi, 2015, International journal of clinical and experimental medicine.

ERBB3-rs2292239 as primary type 1 diabetes association locus among non-HLA genes in Chinese

W. Lu, Chengjun Sun, F. Luo, 2016, Meta gene.

The growth hormone receptor (GHR) exon 3 polymorphism and its correlation with metabolic profiles in obese Chinese children

F. Luo, Lingfeng Cao, R. Cheng, 2011, Pediatric diabetes.

Sulfonylurea in the treatment of neonatal diabetes mellitus children with heterogeneous genetic backgrounds

F. Luo, Lingfeng Cao, Linqi Chen, 2015, Journal of pediatric endocrinology & metabolism : JPEM.

Glycated Hemoglobin (HbA1c) Concentrations Among Children and Adolescents With Diabetes in Middle- and Low-Income Countries, 2010–2019: A Retrospective Chart Review and Systematic Review of Literature

Chengjun Sun, F. Luo, Linqi Chen, 2021, Frontiers in Endocrinology.

Recovered insulin production after thiamine administration in permanent neonatal diabetes mellitus with a novel solute carrier family 19 member 2 (SLC19A2) mutation

Chengjun Sun, F. Luo, R. Cheng, 2018, Journal of diabetes.

Genetic aetiology of primary adrenal insufficiency in Chinese children

Chengjun Sun, F. Luo, Rong Ye, 2020, BMC medical genomics.

Long-acting PEGylated recombinant human growth hormone (Jintrolong) for children with growth hormone deficiency: phase II and phase III multicenter, randomized studies

C. Gong, M. Du, Z. Su, 2017, European journal of endocrinology.

A New Transgenic Mouse Model for the Study of Cell Cycle Control in Megakaryocytes

K. Ravid, D. Ladd, J. Zimmet, 1996, Stem cells.

Clinical evaluation of recombinant human growth hormone injection in children with growth hormone deficiency

C. Gong, M. Du, Huamei Ma, 2009 .

Novel BSCL2 gene mutation E189X in Chinese congenital generalized lipodystrophy child with early onset diabetes mellitus.

W. Kiess, Jing Jin, F. Luo, 2007, European journal of endocrinology.

Novel BSCL 2 gene mutation E 189 X in Chinese congenital generalized lipodystrophy child with early onset diabetes mellitus

W. Kiess, Jing Jin, F. Luo, 2007 .

Mutations in GH1 gene and isolated growth hormone deficiency (IGHD): A familial case of IGHD type I and systematic review.

Chengjun Sun, Bijun Sun, Zhu-hui Zhao, 2021, Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society.