Y. Chi

发表

A compound heterozygous mutation in SLC34A3 causes hereditary hypophosphatemic rickets with hypercalciuria in a Chinese patient.

Xiaodong He, Xiaodong He, X. Xing, 2014, Bone.

Predicting the intervention threshold for initiating osteoporosis treatment among postmenopausal women in China: a cost-effectiveness analysis based on real-world data

Y. Jiang, X. Xing, Mengtao Li, 2019, Osteoporosis International.

Bone Microarchitecture in Obese Postmenopausal Chinese Women: The Chinese Vertebral Osteoporosis Study (ChiVOS)

X. Xing, W. Xia, Yan Jiang, 2022, Frontiers in Endocrinology.

Novel mutations of CYP27B1 gene lead to reduced activity of 1α-hydroxylase in Chinese patients.

Hua Su, T. Yuan, M. Nie, 2012, Bone.

The efficacy and safety of different doses of calcitriol combined with neutral phosphate in X-linked hypophosphatemia: a prospective study

Y. Jiang, X. Xing, Mei Li, 2022, Osteoporosis International.

Bone Volumetric Density, Microarchitecture, and Estimated Bone Strength in Tumor-Induced Rickets/Osteomalacia Versus X-linked Hypophosphatemia in Chinese Adolescents

Xiang Li, X. Li, X. Xing, 2022, Frontiers in Endocrinology.

Early Discrimination Between Tumor‐Induced Rickets/Osteomalacia and X‐Linked Hypophosphatemia in Chinese Children and Adolescents: A Retrospective Case–Control Study

W. Lv, X. Xing, W. Xia, 2021, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Consensus on clinical management of tumor-induced osteomalacia

Jian-min Liu, Z. Sheng, X. Xing, 2021, Chinese medical journal.

Mutation update and long-term outcome after treatment with active vitamin D3 in Chinese patients with pseudovitamin D-deficiency rickets (PDDR)

Xiaoping Zhou, Y. Jiang, X. Xing, 2018, Osteoporosis International.

Clinical characteristics and the influence of rs1800470 in patients with Camurati-Engelmann disease

W. Liu, X. Xing, W. Xia, 2022, Frontiers in Endocrinology.

Iron deficiency plays essential roles in the trigger, treatment, and prognosis of autosomal dominant hypophosphatemic rickets

Y. Jiang, X. Xing, W. Xia, 2020, Osteoporosis International.

Nonremission and Recurrent Tumor‐Induced Osteomalacia: A Retrospective Study

W. Lv, X. Xing, W. Xia, 2019, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Low-Dose Adefovir Dipivoxil May Induce Fanconi Syndrome: Clinical Characteristics and Long-Term follow-up for Chinese Patients

X. Xing, J. Mao, W. Xia, 2015, Antiviral therapy.

Novel mutations of CLCN7 cause autosomal dominant osteopetrosis type II (ADO-II) and intermediate autosomal recessive osteopetrosis (IARO) in Chinese patients

Y. Jiang, X. Xing, O. Wang, 2016, Osteoporosis International.

Bone Impairment in a Large Cohort of Chinese Patients With Tumor‐Induced Osteomalacia Assessed by HR‐pQCT and TBS

W. Lv, S. Fukumoto, X. Xing, 2021, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Tumor‐induced osteomalacia combined with acromegaly: A case report

X. Xing, H. Jing, B. Feng, 2022, Annals of the New York Academy of Sciences.

Na-Cl Co-transporter (NCC) gene inactivation is associated with improved bone microstructure

X. Xing, W. Xia, Yan Jiang, 2022, Osteoporosis International.