Xiao-jie Xu

发表

Genotype-phenotype analysis of a rare type of osteogenesis imperfecta in four Chinese families with WNT1 mutations.

Asan, X. Xing, W. Xia, 2016, Clinica chimica acta; international journal of clinical chemistry.

The analysis of DKK1 polymorphisms in relation to skeletal phenotypes and bone response to alendronate treatment in Chinese postmenopausal women.

X. Xing, W. Xia, Yan Jiang, 2016, Pharmacogenomics.

EFFECTS OF LONG-TERM ALENDRONATE TREATMENT ON A LARGE SAMPLE OF PEDIATRIC PATIENTS WITH OSTEOGENESIS IMPERFECTA.

X. Xing, W. Xia, Mei Li, 2016, Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists.

Recurrent and novel mutations in the NTRK1 gene lead to rare congenital insensitivity to pain with anhidrosis in two Chinese patients.

X. Xing, P. Gao, W. Xia, 2017, Clinica chimica acta; international journal of clinical chemistry.

Two novel mutations in TMEM38B result in rare autosomal recessive osteogenesis imperfecta

Asan, X. Xing, W. Xia, 2016, Journal of Human Genetics.

Extremely low level of serum pigment epithelium-derived factor is a special biomarker of Chinese osteogenesis imperfecta patients with SERPINF1 mutations.

X. Xing, W. Xia, Yan Jiang, 2017, Clinica chimica acta; international journal of clinical chemistry.

Novel Mutations in PLOD2 Cause Rare Bruck Syndrome

Asan, Huanming Yang, X. Xing, 2017, Calcified Tissue International.

Novel mutations in FKBP10 in Chinese patients with osteogenesis imperfecta and their treatment with zoledronic acid

Asan, X. Xing, W. Xia, 2016, Journal of Human Genetics.

A cryptic balanced translocation involving COL1A2 gene disruption cause a rare type of osteogenesis imperfecta.

Asan, X. Xing, W. Xia, 2016, Clinica chimica acta; international journal of clinical chemistry.

Osteogenesis imperfecta type V: Genetic and clinical findings in eleven Chinese patients.

X. Xing, W. Xia, Yan Jiang, 2016, Clinica chimica acta; international journal of clinical chemistry.

Novel mutations in BMP1 induce a rare type of osteogenesis imperfecta.

Asan, X. Xing, W. Xia, 2019, Clinica chimica acta; international journal of clinical chemistry.

SOST polymorphisms and response to alendronate treatment in postmenopausal Chinese women with osteoporosis.

E. Liao, X. Xing, W. Xia, 2015, Pharmacogenomics.

A novel mutation in CLDN16 results in rare familial hypomagnesaemia with hypercalciuria and nephrocalcinosis in a Chinese family.

X. Xing, W. Xia, Yan Jiang, 2016, Clinica chimica acta; international journal of clinical chemistry.

ZOLEDRONIC ACID VERSUS ALENDRONATE IN THE TREATMENT OF CHILDREN WITH OSTEOGENESIS IMPERFECTA: A 2-YEAR CLINICAL STUDY.

X. Xing, W. Xia, O. Wang, 2018, Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists.

Effects of alendronate and alfacalcidol on bone in patients with myasthenia gravis initiating glucocorticoids treatment

Y. Guan, X. Xing, W. Xia, 2018, Clinical endocrinology.

Association Between Geranylgeranyl Pyrophosphate Synthase Gene Polymorphisms and Bone Phenotypes and Response to Alendronate Treatment in Chinese Osteoporotic Women.

X. Xing, W. Xia, Yan Jiang, 2016, Chinese medical sciences journal = Chung-kuo i hsueh k'o hsueh tsa chih.

Systematic Review and Meta-Analysis of Drug-Eluting Balloon and Stent for Infrapopliteal Artery Revascularization

Xue-qiang Fan, Jian-bin Zhang, J. Kong, 2017, Vascular and endovascular surgery.

Novel Mutations in SERPINF1 Result in Rare Osteogenesis Imperfecta Type VI

A. San, Huan-ming Yang, X. Xing, 2016, Calcified Tissue International.

THE CLINICAL CHARACTERISTICS AND EFFICACY OF BISPHOSPHONATES IN AUDLT PATIENTS WITH OSTEOGENESIS IMPERGECTA.

X. Xing, W. Xia, Mei Li, 2016, Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists.

Osteogenesis imperfecta type I: A case report

Jianmin Ren, Xiao-jie Xu, X. Jian, 2014, Experimental and therapeutic medicine.

Novel Mutations in PLOD2 Cause Rare Bruck Syndrome

Asan, Huanming Yang, X. Xing, 2018, Calcified Tissue International.