F. Lv

发表

Repeated Abortion Affects Subsequent Pregnancy Outcomes in BALB/c Mice

Lili Wang, Ning Wang, B. He, 2012, PloS one.

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.

Cost-effectiveness analysis of reformative Bobath rehabilitation versus traditional rehabilitation in post-stroke syndrome

F. Lv, Qiangsan Sun, R. Geng, 2018 .

Clinical characteristics and bisphosphonates treatment of rare pregnancy- and lactation-associated osteoporosis

X. Xing, P. Gao, Jia Zhang, 2018, Clinical Rheumatology.

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 FKBP10 and PLOD2 Cause Rare Bruck Syndrome in Chinese Patients

M. Nie, X. Xing, W. Xia, 2014, PloS one.

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.

Gorham-Stout disease: radiological, histological, and clinical features of 12 cases and review of literature

X. Xing, W. Xia, Yan Jiang, 2016, Clinical Rheumatology.

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.

Gene mutation spectrum and genotype-phenotype correlation in a cohort of Chinese osteogenesis imperfecta patients revealed by targeted next generation sequencing

Asan, Y. Jiang, X. Xing, 2017, Osteoporosis International.

Serum Cytokeratin 19 Fragment, CK19-2G2, as a Newly Identified Biomarker for Lung Cancer

J. Qi, F. Lv, Jia Li, 2014, PloS one.

Molecular analysis of cell-free DNA identifies distinct molecular features in patients with chemosensitive and chemorefractory small cell lung cancer

Xiaoling Chen, Henghui Zhang, F. Lv, 2019, Cancer communications.

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.

Y. Jiang, D. Zhao, X. Xing, 2019, Osteoporosis International.

Novel compound heterozygous mutations in SERPINH1 cause rare autosomal recessive osteogenesis imperfecta type X

Y. Jiang, D. Zhao, X. Xing, 2018, Osteoporosis International.

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.

A novel large fragment deletion in PLS3 causes rare X-linked early-onset osteoporosis and response to zoledronic acid

Y. Jiang, X. Xing, Mei Li, 2017, Osteoporosis International.

Effect of levothyroxine sodium combined with selenium supplement

Hua Fan, Chunping Sun, F. Lv, 2020 .

Novel Mutations in PLOD2 Cause Rare Bruck Syndrome

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

NOTCH3 is a Prognostic Factor and Is Correlated With Immune Tolerance in Gastric Cancer

Yingyong Hou, Henghui Zhang, Qian Li, 2021, Frontiers in Oncology.

The mutational landscape of MSI-H and MSS colorectal cancer.

E. Li, Henghui Zhang, Tianshu Liu, 2019, Journal of Clinical Oncology.

Successful treatment of type B insulin resistance with mixed connective tissue disease by pulse glucocorticoids and cyclophosphamide

Jiuliang Zhao, Yuxiu Li, Hongbo Yang, 2017, Journal of diabetes investigation.

Postoperative dynamic changes in the concentration of CK19-2G2 in lung cancer patients and the clinical value of this marker

J. Qi, F. Lv, Ji-wen Wang, 2015, Tumor Biology.

Gene mutation spectrum and genotype-phenotype correlation in a cohort of Chinese osteogenesis imperfecta patients revealed by targeted next generation sequencing

Asan, Y. Jiang, X. Xing, 2017, Osteoporosis International.