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The diagnostic dilemma of tumor induced osteomalacia: a retrospective analysis of 144 cases

Endocrine Journal, 2017, Vol.64(7), pp.675-683

2017

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Global guidance for the recognition, diagnosis, and management of tumor‐induced osteomalacia

Journal of internal medicine, 2023-03, Vol.293 (3), p.309-328

2023

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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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Primary hypertrophic osteoarthropathy related gastrointestinal complication has distinctive clinical and pathological characteristics: two cases report and review of the literature

Orphanet journal of rare diseases, 2019-12, Vol.14 (1), p.297-297, Article 297

2019

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Impaired bone strength and bone microstructure in a novel early-onset osteoporotic rat model with a clinically relevant PLS3 mutation

eLife, 2023-04, Vol.12

2023

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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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A novel homozygous mutation of the calcium-sensing receptor gene associated with apparent autosomal recessive inheritance of familial hypocalciuric hypercalcemia

Chinese medical journal, 2021-08, Vol.134 (15), p.1869-1871

2021

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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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Management of fracture risk in patients with diabetes—Chinese Expert Consensus

Journal of diabetes, 2019-11, Vol.11 (11), p.906-919

2019

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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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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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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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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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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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Unique mutation spectrum of progressive pseudorheumatoid dysplasia in the Chinese population: a retrospective genotype–phenotype analysis of 105 patients

World journal of pediatrics : WJP, 2023-07, Vol.19 (7), p.674-686

2023

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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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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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A novel variant in AIRE causing a rare, non‑classical autoimmune polyendocrine syndrome type 1

Molecular medicine reports, 2020-08, Vol.22 (2), p.1285-1294

2020

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The diagnostic dilemma of tumor induced osteomalacia: a retrospective analysis of 144 cases

Global guidance for the recognition, diagnosis, and management of tumor‐induced osteomalacia

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

Primary hypertrophic osteoarthropathy related gastrointestinal complication has distinctive clinical and pathological characteristics: two cases report and review of the literature

Impaired bone strength and bone microstructure in a novel early-onset osteoporotic rat model with a clinically relevant PLS3 mutation

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

A novel homozygous mutation of the calcium-sensing receptor gene associated with apparent autosomal recessive inheritance of familial hypocalciuric hypercalcemia

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

Consensus on clinical management of tumor-induced osteomalacia

Management of fracture risk in patients with diabetes—Chinese Expert Consensus

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

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

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

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

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

Unique mutation spectrum of progressive pseudorheumatoid dysplasia in the Chinese population: a retrospective genotype–phenotype analysis of 105 patients

Novel variants in COL2A1 causing rare spondyloepiphyseal dysplasia congenita

Novel Mutations in SERPINF1 Result in Rare Osteogenesis Imperfecta Type VI

A novel variant in AIRE causing a rare, non‑classical autoimmune polyendocrine syndrome type 1

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