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Results of search for 'au:"Xing, Xiaoping"', page 2 of 5
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Authors
Cao, Yuhua
Chen, Limeng
Chen, Zhike
He, Shuli
Hu, Yingying
Jiang, Yan
Li, Mei
Meng, Xunwu
Nie, Min
Pang, Qianqian
Pei, Yu
Sun, Yue
Wang, Ou
Wang, Wenbo
Xia, Weibo
Xing, Xiaoping
Xu, Ling
Yu, Wei
Yuan, Tao
Zhou, Xueying
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Asian People
Bone Density
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Child, Preschool
China
DNA Mutational Analysis
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Fibroblast Growth Factor-23
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blood
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21.
Four novel mutations in the
[electronic resource]
by
Xu, Lijun
Pang, Qianqian
Jiang, Yan
Wang, Ou
Li, Mei
Xing, Xiaoping
Xia, Weibo
Producer:
20190405
In:
Bioscience reports
vol. 38
Online resources:
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22.
Clinical phenotypes of Chinese primary hyperparathyroidism patients are associated with the calcium-sensing receptor gene R990G polymorphism.
[electronic resource]
by
Han, Guiyan
Wang, Ou
Nie, Min
Zhu, Yan
Meng, Xunwu
Hu, Yingying
Liu, Huaicheng
Xing, Xiaoping
Producer:
20131119
In:
European journal of endocrinology
vol. 169
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23.
A novel missense mutation in
[electronic resource]
by
Li, Lujiao
Zhao, Dichen
Zheng, Wenbin
Wang, Ou
Jiang, Yan
Xia, Weibo
Xing, Xiaoping
Li, Mei
Producer:
20200413
In:
Bioscience reports
vol. 39
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24.
Atypical Femoral Fracture Associated With Overuse of Bisphosphonate Evaluated by High-Resolution Peripheral Quantitative Computed Tomography (HR-pQCT).
[electronic resource]
by
Cui, Lijia
Xu, Yuping
Xu, Qiming
Jiang, Yan
Wang, Ou
Li, Mei
Xing, Xiaoping
Xia, Weibo
Producer:
20210726
In:
Journal of clinical densitometry : the official journal of the International Society for Clinical Densitometry
vol. 23
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25.
Genetic Screening in a Large Chinese Cohort of Childhood Onset Hypoparathyroidism by Next-Generation Sequencing Combined with TBX1-MLPA.
[electronic resource]
by
Wang, Yabing
Nie, Min
Wang, Ou
Li, Yuepeng
Jiang, Yan
Li, Mei
Xia, Weibo
Xing, Xiaoping
Producer:
20200910
In:
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
vol. 34
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26.
China type 2 diabetes treatment status survey of treatment pattern of oral drugs users
[electronic resource]
by
Ji, Linong
Lu, Juming
Weng, Jianping
Jia, Weiping
Tian, Haoming
Zhu, Dalong
Xing, Xiaoping
Guo, Lixin
Producer:
20151029
In:
Journal of diabetes
vol. 7
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27.
MEN1 c.825‑1G>A mutation in a family with multiple endocrine neoplasia type 1: A case report.
[electronic resource]
by
Ning, Zhiwei
Wang, Ou
Meng, Xunwu
Xing, Xiaoping
Xia, Weibo
Jiang, Yan
Li, Mei
Xu, Yuan
Producer:
20160802
In:
Molecular medicine reports
vol. 12
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28.
Two novel CAII mutations causing carbonic anhydrase II deficiency syndrome in two unrelated Chinese families.
[electronic resource]
by
Pang, Qianqian
Qi, Xuan
Jiang, Yan
Wang, Ou
Li, Mei
Xing, Xiaoping
Dong, Jin
Xia, Weibo
Producer:
20160408
In:
Metabolic brain disease
vol. 30
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29.
Tortuous but successful road to achieving the diagnosis of cyclic Cushing's disease.
[electronic resource]
by
Li, Jiapei
Lu, Lin
Li, Yiping
Li, Yuepeng
Lian, Xiaolan
Lu, Zhaolin
Xing, Xiaoping
Yang, Hongbo
Producer:
20200306
In:
Journal of paediatrics and child health
vol. 54
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30.
Clinical and genetic findings in a Chinese family with VDR-associated hereditary vitamin D-resistant rickets.
[electronic resource]
by
Pang, Qianqian
Qi, Xuan
Jiang, Yan
Wang, Ou
Li, Mei
Xing, Xiaoping
Dong, Jin
Xia, Weibo
Producer:
20160713
In:
Bone research
vol. 4
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31.
[Alendronate in postmenopausal women with osteopenia and osteoporosis: effects on bone mineral density during treatment and after withdrawal].
[electronic resource]
by
Jiang, Yan
Li, Mei
Xia, Weibo
Xing, Xiaoping
Yu, Wei
Tian, Junping
Meng, Xunwu
Zhou, Xueying
Producer:
20030728
In:
Zhonghua yi xue za zhi
vol. 82
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32.
The first mutation identified in a Chinese acrodysostosis patient confirms a p.G289E variation of PRKAR1A causes acrodysostosis.
[electronic resource]
by
Li, Nan
Nie, Min
Li, Mei
Jiang, Yan
Xing, Xiaoping
Wang, Ou
Li, Chunlin
Xia, Weibo
Producer:
20150330
In:
International journal of molecular sciences
vol. 15
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33.
CLINICAL AND GENETIC FINDINGS IN A CHINESE COHORT OF PATIENTS WITH DIGEORGE SYNDROME-RELATED HYPOPARATHYROIDISM.
[electronic resource]
by
Wang, Yabing
Wang, Ou
Nie, Min
Li, Yuepeng
Jiang, Yan
Li, Mei
Xia, Weibo
Xing, Xiaoping
Producer:
20200819
In:
Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists
vol. 26
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34.
A Mutation in CTSK Gene in an Autosomal Recessive Pycnodysostosis Family of Chinese Origin.
[electronic resource]
by
Huang, Xianglan
Qi, Xuan
Li, Mei
Wang, Ou
Jiang, Yan
Xing, Xiaoping
Hu, Ying Ying
Xia, Weibo
Producer:
20160301
In:
Calcified tissue international
vol. 96
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35.
Glucose tolerance and insulin responsiveness in Gitelman syndrome patients.
[electronic resource]
by
Yuan, Tao
Jiang, Lanping
Chen, Chen
Peng, Xiaoyan
Nie, Min
Li, Xuemei
Xing, Xiaoping
Li, Xuewang
Chen, Limeng
Publication details:
Endocrine connections
May 2017
In:
Endocrine connections
vol. 6
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36.
Structured self-monitoring of blood glucose regimens improve glycemic control in poorly controlled Chinese patients on insulin therapy: Results from COMPASS.
[electronic resource]
by
Ji, Linong
Su, Qing
Feng, Bo
Shan, Zhongyan
Hu, Renming
Xing, Xiaoping
Xue, Yaoming
Yang, Tao
Hua, Yanyin
Producer:
20170731
In:
Journal of diabetes
vol. 9
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37.
Earlier Onset in Autosomal Dominant Hypophosphatemic Rickets of R179 than R176 Mutations in Fibroblast Growth Factor 23: Report of 20 Chinese Cases and Review of the Literature.
[electronic resource]
by
Liu, Chang
Zhao, Zhen
Wang, Ou
Li, Mei
Xing, Xiaoping
Hsieh, Evelyn
Fukumoto, Seiji
Jiang, Yan
Xia, Weibo
Producer:
20201013
In:
Calcified tissue international
vol. 105
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38.
The ER Lumenal Hsp70 Protein FpLhs1 Is Important for Conidiation and Plant Infection in
[electronic resource]
by
Chen, Linlin
Geng, Xuejing
Ma, Yuming
Zhao, Jingya
Chen, Wenbo
Xing, Xiaoping
Shi, Yan
Sun, Bingjian
Li, Honglian
Publication details:
Frontiers in microbiology
2019
In:
Frontiers in microbiology
vol. 10
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39.
Hyperthyroidism caused by an ectopic thyrotropin-secreting tumor of the nasopharynx: a case report and review of the literature.
[electronic resource]
by
Tong, Anli
Xia, Weibo
Qi, Fang
Jin, Zimeng
Yang, Di
Zhang, Zhuhua
Li, Fang
Xing, Xiaoping
Lian, Xiaolan
Producer:
20150518
In:
Thyroid : official journal of the American Thyroid Association
vol. 23
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40.
Novel mutations in FKBP10 and PLOD2 cause rare Bruck syndrome in Chinese patients.
[electronic resource]
by
Zhou, Peiran
Liu, Yi
Lv, Fang
Nie, Min
Jiang, Yan
Wang, Ou
Xia, Weibo
Xing, Xiaoping
Li, Mei
Producer:
20150616
In:
PloS one
vol. 9
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