Search Results - "Ma, Huamei"
-
1
Etiology of primary adrenal insufficiency in children: a 29-year single-center experience
Published in Journal of pediatric endocrinology & metabolism : JPEM (26-06-2019)“…Background Primary adrenal insufficiency (PAI) in children is a rare condition and potentially lethal. The clinical characteristics are non-specific. It may be…”
Get more information
Journal Article -
2
Aldosterone signaling defect in young infants: single-center report and review
Published in BMC endocrine disorders (09-07-2021)“…Aldosterone (Ald) is a crucial factor in maintaining electrolyte and water homeostasis. Defect in either its synthesis or function causes salt wasting (SW)…”
Get full text
Journal Article -
3
Novel genotypes and phenotypes among Chinese patients with Floating-Harbor syndrome
Published in Orphanet journal of rare diseases (14-06-2019)“…Floating-Harbor syndrome (FHS) is a rare syndromic short stature disorder caused by truncating variants in SRCAP. Few Chinese FHS patients had been reported so…”
Get full text
Journal Article -
4
A Multicenter Survey of Type I Diabetes Mellitus in Chinese Children
Published in Frontiers in endocrinology (Lausanne) (15-06-2021)“…To investigate the features and treatment status of children with type 1 diabetes mellitus (T1DM) in China. We recruited patients <14 years of age with T1DM…”
Get full text
Journal Article -
5
The pubertal development mode of Chinese girls with turner syndrome undergoing hormone replacement therapy
Published in BMC endocrine disorders (11-07-2019)“…Further knowledge about the pubertal development mode of girls with Turner syndrome (TS) who have undergone hormone replacement therapy (HRT) is beneficial to…”
Get full text
Journal Article -
6
Gonadal Y-chromosome mosaicism with 45, X Turner syndrome complicated with bilateral HCG-secreting gonadoblastoma
Published in Frontiers in pediatrics (22-11-2022)“…We report a rare case of bilateral HCG-secreting gonadoblastomas (Gb) in a 5.25-year-old girl of 45, X Turner syndrome (TS) with gonadal Y chromosome…”
Get full text
Journal Article -
7
Near-final height in 82 Chinese patients with congenital adrenal hyperplasia due to classic 21-hydroxylase deficiency: a single-center study from China
Published in Journal of pediatric endocrinology & metabolism : JPEM (01-07-2016)“…The objective of this study was to identify variables that might interfere with reaching the near final height (NFH) in Congenital adrenal hyperplasia (CAH)…”
Get more information
Journal Article -
8
Effect of long-acting PEGylated growth hormone for catch-up growth in children with idiopathic short stature: a 2-year real-world retrospective cohort study
Published in European journal of pediatrics (01-10-2024)“…Several evidence gaps exist regarding the use of long-acting polyethylene glycol recombinant human growth hormone (PEG-rhGH) in children with idiopathic short…”
Get full text
Journal Article -
9
Low serum adiponectin levels are associated with reduced insulin sensitivity and lipid disturbances in short children born small for gestational age
Published in Clinical endocrinology (Oxford) (01-07-2015)“…Summary Background Being born as small for gestational age (SGA) has an increased risk of developing metabolic/cardiovascular disturbances in later life. The…”
Get full text
Journal Article -
10
Long-term Pegylated GH for Children With GH Deficiency: A Large, Prospective, Real-world Study
Published in The journal of clinical endocrinology and metabolism (01-08-2023)“…Abstract Context The evidence of long-term polyethylene glycol recombinant human GH (PEG-rhGH) in pediatric GH deficiency (GHD) is limited. Objective This…”
Get full text
Journal Article -
11
Efficacy of letrozole in treatment of male adolescents with idiopathic short stature
Published in Zhejiang da xue xue bao. Journal of Zhejiang University. Medical sciences. Yi xue ban (25-05-2020)“…To evaluate the efficacy and safety of aromatase inhibitor letrozole in treatment of male adolescents with idiopathic short stature (ISS). Seventy five boys…”
Get full text
Journal Article -
12
Estrogen stimulates cell proliferation and regulates the expression of proteins in C-type natriuretic peptide signaling pathway during chondrogenesis in ATDC5 cells
Published in Zhonghua er ke za zhi (01-08-2014)“…To investigate the effect of estrogen on cell proliferation and expression of proteins of C-type natriuretic peptide (CNP), natriuretic peptides B receptor…”
Get more information
Journal Article -
13
Postreceptor crosstalk on PI3K/Akt between GH and insulin in non-catch-up growth rats born small for gestational age
Published in Hormone research (01-01-2008)“…Children born small for gestational age (SGA) are at increased risk for short stature and type 2 diabetes mellitus as a result of growth hormone (GH)…”
Get more information
Journal Article -
14
Molecular Genetic Diagnostics of Prader-Willi Syndrome: a Validation of Linkage Analysis for the Chinese Population
Published in Journal of genetics and genomics (01-10-2007)“…Prader-Willi Syndrome (PWS) is a genetic disorder that is difficult to detect, particularly at an early age. PWS is caused by disruption of normal,…”
Get full text
Journal Article -
15
Clinical evaluation of recombinant human growth hormone injection in children with growth hormone deficiency
Published in Frontiers of medicine (2009)“…Recombinant human growth hormone (rhGH) has been widely used in the clinical treatment of growth hormone deficiency. To simplify the injection process and…”
Get full text
Journal Article -
16
来曲唑改善青春期特发性身材矮小症男性患儿成年身高的疗效评价
Published in Zhejiang da xue xue bao. Journal of Zhejiang University. Medical sciences. Yi xue ban (25-06-2020)Get full text
Journal Article