日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Age- and sex-specific reference intervals and determinants of plasma vitamin B6 metabolites in healthy Chinese adults

健康中国成年人血浆维生素B6代谢物的年龄和性别特异性参考区间及其决定因素

Mei, Yazhao; Wang, Ziyuan; Shen, Li; Zhang, Zhenlin; Yue, Hua; Zhang, Hao; Gu, Jiemei; Hu, Weiwei; Li, Shanshan; Gao, Chao; Wei, Zhe; Xu, Yang; Wang, Jie; Gao, Gao; Wang, Chun

Reference Intervals for 24-Hour Urinary Calcium Excretion and Its Association With Bone Metabolism: A Multicenter Study

24小时尿钙排泄参考区间及其与骨代谢的关系:一项多中心研究

Shen, Li; Zhang, Hao; Lu, Qi; Li, Shanshan; Mei, Yazhao; Gao, Chao; Yue, Hua; Yu, Xiangtian; Yao, Qi; Huo, Yanan; Zeng, Yuhong; Jiang, Yin; Xie, Zhongjian; Chao, Aijun; Jin, Xiaolan; Yu, Guangjun; Mao, Li; Zhang, Zhenlin

Clinical Benefits of Denosumab vs Zoledronate in Postmenopausal Women Previously Treated with Alendronate: A Two-Year Retrospective Study

地诺单抗与唑来膦酸在既往接受过阿仑膦酸钠治疗的绝经后妇女中的临床获益:一项为期两年的回顾性研究

Wang, Ziyuan; Mei, Yazhao; Shen, Li; Gu, Jiemei; Ren, Na; Wang, Ya; Zhang, Zhenlin; Wang, Chun

Denosumab in patients with osteogenesis imperfecta and a historical control study with alendronate

地诺单抗治疗成骨不全症患者及一项阿仑膦酸钠历史对照研究

Mei, Yazhao; Cai, Shiya; Jiang, Yunyi; Tian, Yuan; Shen, Li; Gu, Jiemei; Wang, Chun; Zhang, Zhenlin; Zhang, Hao

Clinical features, treatment, and follow-up of OPPG and high-bone-mass disorders: LRP5 is a key regulator of bone mass.

OPPG 和高骨量疾病的临床特征、治疗和随访:LRP5 是骨量的关键调节因子

Ren Na, Lv Shanshan, Li Xiang, Shao Chong, Wang Ziyuan, Mei Yazhao, Yang Wendi, Fu Wenzhen, Hu Yunqiu, Sha Ling, Hu Weiwei, Zhang Zhenlin, Wang Chun

The vitamin D status in a Chinese osteogenesis imperfecta population and its correlation with bone metabolic markers and bone density

中国成骨不全患者维生素D水平及其与骨代谢标志物和骨密度的相关性

Jiang, Yunyi; Mei, Yazhao; Tian, Yuan; Shen, Li; Xu, Shuqin; Zhang, Hao; Zhang, Zhenlin

Echocardiographic abnormalities and joint hypermobility in Chinese patients with Osteogenesis imperfecta

中国成骨不全患者的心脏超声异常和关节过度活动

Mei, Yazhao; Jiang, Yunyi; Shen, Li; Meng, Zheying; Zhang, Zhenlin; Zhang, Hao

Muscle and bone characteristics of a Chinese family with spinal muscular atrophy, lower extremity predominant 1 (SMALED1) caused by a novel missense DYNC1H1 mutation.

中国一个患有脊髓性肌萎缩症(下肢为主型 1 型,SMALED1)的家庭的肌肉和骨骼特征,该病由一种新的 DYNC1H1 错义突变引起

Mei Yazhao, Jiang Yunyi, Zhang Zhenlin, Zhang Hao

Comparing Clinical and Genetic Characteristics of De Novo and Inherited COL1A1/COL1A2 Variants in a Large Chinese Cohort of Osteogenesis Imperfecta

比较中国大型成骨不全患者队列中新发和遗传性 COL1A1/COL1A2 变异的临床和遗传特征

Mei, Yazhao; Zhang, Hao; Zhang, Zhenlin