Publications by authors named "Fuying Song"

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A Novel Y-Shaped Pegylated Recombinant Human Growth Hormone for Children With Growth Hormone Deficiency.
Yan Liang, Haiyan Wei, Fan Yang, Hua Zhang, Linqi Chen, Fuying Song

J Clin Endocrinol Metab· July 2025

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Clinical, genetic characteristics and long-term follow-up of sitosterolemia in children.
Shuyue Huang, Mu Du, Xi'ou Wang, Yi Liu, Fuying Song

Transl Pediatr· February 2025

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Noonan syndrome and Noonan-like syndrome with loose anagen hair: rare phenotypes may emerge during follow-up.
Ziqin Liu, Jianming Lai, Fuying Song

Transl Pediatr· July 2024

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Plasma exchange treatment of a diabetic ketoacidosis child with hyperlipidemia to avoid pancreatitis: a case report.
Shuyue Huang, Fuying Song, Kang Gao, Yi Song, Xiaobo Chen

Front Pediatr· June 2024

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[Clinical characteristics and genetic analysis of three children with Congenital chlorine diarrhea].
Hui Yin, Xiaobo Chen, Fuying Song, Hui Wang, Mu Du

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· February 2023

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The pharmacokinetic and pharmacodynamic properties and short-term outcome of a novel once-weekly PEGylated recombinant human growth hormone for children with growth hormone deficiency.
Yan Liang, Cai Zhang, Haiyan Wei, Hongwei Du, Gaixiu Zhang, Fuying Song

Front Endocrinol (Lausanne)· August 2022

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[Clinical and genetic analysis of a patient with isolated 17,20 lyase deficiency presenting with pubertal gynecomastia].
Hui Yin, Xiaobo Chen, Ziqin Liu, Fuying Song, Kang Gao

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· July 2022

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[Analysis of clinical features and genetic variants among 12 children with Gitelman syndrome].
Qian Dong, Fuying Song, Guohong Li, Mu Du, Xiaobo Chen

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· June 2021

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[Clinical and genetic analysis of a child with neonatal severe parathyroidism].
Qian Dong, Fuying Song, Mu Du, Mingfang Qiu, Xiaobo Chen

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· November 2020

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Next-Generation Sequencing Revealed Disease-Causing Variants in Two Genes in a Patient With Combined Features of Spherocytosis and Antley-Bixler Syndrome With Genital Anomalies and Disordered Steroidogenesis.
Fuying Song, Shunqiao Feng, Xiang Shen, Mu Du, Hui Yin

Front Genet· August 2020

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[Clinical and genetic characteristics of glucose transporter type 1 deficiency syndrome].
Yan-yan Liu, Xin-hua Bao, Shuang Wang, Na Fu, Xiao-yan Liu, Fu-ying Song

Zhonghua Er Ke Za Zhi· June 2013

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Allelic variations of glut-1 deficiency syndrome: the chinese experience.
Yanyan Liu, Xinhua Bao, Dong Wang, Na Fu, Xiaoying Zhang, Fuying Song

Pediatr Neurol· July 2012

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X chromosome inactivation in Rett Syndrome and its correlations with MECP2 mutations and phenotype.
Xinhua Bao, Shengling Jiang, Fuying Song, Hong Pan, Meirong Li

J Child Neurol· January 2008

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[X chromosome inactivation patterns in patients with Rett syndrome and their mothers and the parental origin of the priority inactive X chromosome].
Sheng-ling Jiang, Xin-hua Bao, Fu-ying Song, Hong Pan, Mei-rong Li

Zhonghua Er Ke Za Zhi· September 2006

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[Clinical feature of Rett syndrome and MeCP2 genotype/phenotype correlation analysis].
Xin-hua Bao, Hong Pan, Fu-ying Song, Xi-ru Wu

Zhonghua Er Ke Za Zhi· April 2004

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