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Rapidly increasing rates of hip fracture in Beijing, China

Journal of bone and mineral research, 2012-01, Vol.27 (1), p.125-129

2012

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Tumor-induced osteomalacia: An important cause of adult-onset hypophosphatemic osteomalacia in China: Report of 39 cases and review of the literature

Journal of bone and mineral research, 2012-09, Vol.27 (9), p.1967-1975

2012

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The roles of sclerostin and irisin on bone and muscle of orchiectomized rats

BMC musculoskeletal disorders, 2022-12, Vol.23 (1), p.1049-1049, Article 1049

2022

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Specific Characteristic of Hyperplastic Callus in a Larger Cohort of Osteogenesis Imperfecta Type V

Calcified tissue international, 2022-04, Vol.110 (4), p.451-463

2022

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Health-related quality of life of men with primary osteoporosis and its changes after bisphosphonates treatment

BMC musculoskeletal disorders, 2023-04, Vol.24 (1), p.309-309, Article 309

2023

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Characterization of the clinical and genetic spectrum of autoimmune polyendocrine syndrome type 1 in Chinese case series

Orphanet journal of rare diseases, 2021-07, Vol.16 (1), p.296-296, Article 296

2021

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Effects of Bisphosphonates on Osteoporosis Induced by Duchenne Muscular Dystrophy: A Prospective Study

Endocrine practice, 2020-12, Vol.26 (12), p.1477-1485

2020

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

Clinical rheumatology, 2018-11, Vol.37 (11), p.3141-3150

2018

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A novel mutant Na+/HCO3− cotransporter NBCe1 in a case of compound‐heterozygous inheritance of proximal renal tubular acidosis

The Journal of physiology, 2016-11, Vol.594 (21), p.6267-6286

2016

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

Clinical Rheumatology, 2016-03, Vol.35 (3), p.813-823

2016

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A novel mutation in PLS3 causes extremely rare X‐linked osteogenesis imperfecta

Molecular genetics & genomic medicine, 2020-12, Vol.8 (12), p.e1525-n/a

2020

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The role of osteocalcin in regulation of glycolipid metabolism and muscle function in children with osteogenesis imperfecta

Frontiers in endocrinology (Lausanne), 2022-08, Vol.13, p.898645-898645

2022

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URAT1 mutations cause renal hypouricaemia combined with Fanconi syndrome in a Chinese patient

Nephrology (Carlton, Vic.), 2018-08, Vol.23 (8), p.797-798

2018

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Genotype-phenotype relationship in a large cohort of osteogenesis imperfecta patients with COL1A1 mutations revealed by a new scoring system

Chinese medical journal, 2019-01, Vol.132 (2), p.145-153

2019

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

Journal of human genetics, 2016-06, Vol.61 (6), p.539-545

2016

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Consensus on clinical management of tumor-induced osteomalacia

Chinese medical journal, 2021-06, Vol.134 (11), p.1264-1266

2021

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Somatostatin Treatment for Ectopic ACTH Syndrome due to Pancreatic Neuroendocrine Tumors: Review of the Literature

International journal of endocrinology, 2022-02, Vol.2022, p.6283706-10

2022

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Metabolomics Analysis of Electroacupuncture Pretreatment Induced Neuroprotection on Mice with Ischemic Stroke

The American journal of Chinese medicine (1979), 2023-01, Vol.51 (5), p.1127-1151

2023

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Pseudohypoparathyroidism during pregnancy and the postpartum period: A case series of five patients

Frontiers in endocrinology (Lausanne), 2022-11, Vol.13, p.1050305-1050305

2022

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

Journal of human genetics, 2017-02, Vol.62 (2), p.205-211

2017

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Novel Mutations in SERPINF1 Result in Rare Osteogenesis Imperfecta Type VI

Calcified tissue international, 2017-01, Vol.100 (1), p.55-66

2017

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Novel variants in COL2A1 causing rare spondyloepiphyseal dysplasia congenita

Molecular genetics & genomic medicine, 2020-03, Vol.8 (3), p.e1139-n/a

2020

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FpPDE1 function of Fsarium pseudograminearum on pathogenesis in wheat

Journal of Integrative Agriculture, 2017-11, Vol.16 (11), p.2504-2512

2017

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A Novel De novo GATA-binding Protein 3 Mutation in a Patient with Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia Syndrome

Chinese medical journal, 2017-06, Vol.130 (11), p.1378-1380

2017

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Safety and efficacy of cyclooxygenase-2 inhibition for treatment of primary hypertrophic osteoarthropathy: A single-arm intervention trial

Journal of orthopaedic translation, 2019-07, Vol.18, p.109-118

2019

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Rapidly increasing rates of hip fracture in Beijing, China

Tumor-induced osteomalacia: An important cause of adult-onset hypophosphatemic osteomalacia in China: Report of 39 cases and review of the literature

The roles of sclerostin and irisin on bone and muscle of orchiectomized rats

Specific Characteristic of Hyperplastic Callus in a Larger Cohort of Osteogenesis Imperfecta Type V

Health-related quality of life of men with primary osteoporosis and its changes after bisphosphonates treatment

Characterization of the clinical and genetic spectrum of autoimmune polyendocrine syndrome type 1 in Chinese case series

Effects of Bisphosphonates on Osteoporosis Induced by Duchenne Muscular Dystrophy: A Prospective Study

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

A novel mutant Na+/HCO3− cotransporter NBCe1 in a case of compound‐heterozygous inheritance of proximal renal tubular acidosis

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

A novel mutation in PLS3 causes extremely rare X‐linked osteogenesis imperfecta

The role of osteocalcin in regulation of glycolipid metabolism and muscle function in children with osteogenesis imperfecta

URAT1 mutations cause renal hypouricaemia combined with Fanconi syndrome in a Chinese patient

Genotype-phenotype relationship in a large cohort of osteogenesis imperfecta patients with COL1A1 mutations revealed by a new scoring system

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

Consensus on clinical management of tumor-induced osteomalacia

Somatostatin Treatment for Ectopic ACTH Syndrome due to Pancreatic Neuroendocrine Tumors: Review of the Literature

Metabolomics Analysis of Electroacupuncture Pretreatment Induced Neuroprotection on Mice with Ischemic Stroke

Pseudohypoparathyroidism during pregnancy and the postpartum period: A case series of five patients

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

Novel Mutations in SERPINF1 Result in Rare Osteogenesis Imperfecta Type VI

Novel variants in COL2A1 causing rare spondyloepiphyseal dysplasia congenita

FpPDE1 function of Fsarium pseudograminearum on pathogenesis in wheat

A Novel De novo GATA-binding Protein 3 Mutation in a Patient with Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia Syndrome

Safety and efficacy of cyclooxygenase-2 inhibition for treatment of primary hypertrophic osteoarthropathy: A single-arm intervention trial

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