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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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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 Hemoglobin, Albumin, Lymphocyte, and Platelet (HALP) Score in Patients with Small Cell Lung Cancer Before First-Line Treatment with Etoposide and Progression-Free Survival

Medical science monitor, 2019-07, Vol.25, p.5630-5639

2019

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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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USP13 regulates ferroptosis in chicken follicle granulosa cells by deubiquitinating ATG7

Poultry science, 2024-11, Vol.103 (11), p.104209, Article 104209

2024

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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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Mitochondrial DNA hypomethylation in chrome plating workers

Toxicology letters, 2016-01, Vol.243, p.1-6

2016

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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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Downregulation of CKS1B restrains the proliferation, migration, invasion and angiogenesis of retinoblastoma cells through the MEK/ERK signaling pathway

International journal of molecular medicine, 2019-07, Vol.44 (1), p.103-114

2019

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Which one is the best in treating deep venous thrombosis -- percutaneous mechanical thrombectomy, catheter-directed thrombolysis or combination of them?

Journal of cardiothoracic surgery, 2024-07, Vol.19 (1), p.423-8, Article 423

2024

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Metabolomics and pharmacodynamic analysis reveal the therapeutic role of Prunella vulgaris oil on intrauterine adhesion rats

Journal of pharmaceutical and biomedical analysis, 2022-02, Vol.209, p.114532-114532, Article 114532

2022

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Drivers and mediators of healthcare workers’ anxiety in one of the most affected hospitals by COVID-19: a qualitative analysis

BMJ open, 2021-03, Vol.11 (3), p.e045048-e045048

2021

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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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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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Use of a combination of diaphragmatic ultrasound and muscle relaxation monitoring in predicting post-extubation adverse respiratory events among elderly patients in an anesthesia intensive care unit

BMC pulmonary medicine, 2023-12, Vol.23 (1), p.503-503, Article 503

2023

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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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Delayed coronary artery occlusion after transcatheter aortic valve replacement and chimney stenting: a case report

BMC cardiovascular disorders, 2021-09, Vol.21 (1), p.451-5, Article 451

2021

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Allele-specific PCR for detecting the deafness-associated mitochondrial 12S rRNA mutations

Gene, 2016-10, Vol.591 (1), p.148-152

2016

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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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Broad genic repression domains signify enhanced silencing of oncogenes

Nature communications, 2020-11, Vol.11 (1), p.5560-5560, Article 5560

2020

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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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MiR-152 influences osteoporosis through regulation of osteoblast differentiation by targeting RICTOR

Pharmaceutical biology, 2019-01, Vol.57 (1), p.586-594

2019

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

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 Hemoglobin, Albumin, Lymphocyte, and Platelet (HALP) Score in Patients with Small Cell Lung Cancer Before First-Line Treatment with Etoposide and Progression-Free Survival

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

USP13 regulates ferroptosis in chicken follicle granulosa cells by deubiquitinating ATG7

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

Mitochondrial DNA hypomethylation in chrome plating workers

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

Downregulation of CKS1B restrains the proliferation, migration, invasion and angiogenesis of retinoblastoma cells through the MEK/ERK signaling pathway

Which one is the best in treating deep venous thrombosis -- percutaneous mechanical thrombectomy, catheter-directed thrombolysis or combination of them?

Metabolomics and pharmacodynamic analysis reveal the therapeutic role of Prunella vulgaris oil on intrauterine adhesion rats

Drivers and mediators of healthcare workers’ anxiety in one of the most affected hospitals by COVID-19: a qualitative analysis

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

Novel variants in COL2A1 causing rare spondyloepiphyseal dysplasia congenita

Use of a combination of diaphragmatic ultrasound and muscle relaxation monitoring in predicting post-extubation adverse respiratory events among elderly patients in an anesthesia intensive care unit

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

Delayed coronary artery occlusion after transcatheter aortic valve replacement and chimney stenting: a case report

Allele-specific PCR for detecting the deafness-associated mitochondrial 12S rRNA mutations

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

Broad genic repression domains signify enhanced silencing of oncogenes

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

MiR-152 influences osteoporosis through regulation of osteoblast differentiation by targeting RICTOR

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