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Health-related quality of life in men with osteoporosis: a systematic review and meta-analysis

Endocrine, 2021-11, Vol.74 (2), p.270-280

2021

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The epidemiology of osteoporosis, associated fragility fractures, and management gap in China

Archives of osteoporosis, 2019-12, Vol.14 (1), p.32, Article 32

2019

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A Chinese case of CHST3-related skeletal dysplasia and a systematic review

Endocrine, 2023-06, Vol.80 (3), p.658-668

2023

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Shear wave elastography for differentiating parathyroid neoplasms with malignant diagnosis or uncertain malignant potential from parathyroid adenomas: initial experience

Cancer imaging, 2022-11, Vol.22 (1), p.1-64, Article 64

2022

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Novel AQP2 Mutations and Clinical Characteristics in Seven Chinese Families With Congenital Nephrogenic Diabetes Insipidus

Frontiers in endocrinology (Lausanne), 2021-06, Vol.12, p.686818-686818

2021

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Associations between FGF21, osteonectin and bone turnover markers in type 2 diabetic patients with albuminuria

Journal of diabetes and its complications, 2017-03, Vol.31 (3), p.583-588

2017

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Early bone loss in patients with obstructive sleep apnea: a cross-sectional study

BMC pulmonary medicine, 2024-01, Vol.24 (1), p.28-28, Article 28

2024

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Chinese bone turnover marker study: reference ranges for C-terminal telopeptide of type I collagen and procollagen I N-terminal peptide by age and gender

PloS one, 2014-08, Vol.9 (8), p.e103841-e103841

2014

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A 105 kb interstitial insertion in the Xq27.1 palindrome from pseudoautosomal region PAR1 causes a novel X-linked recessive compound phenotype

Journal of translational medicine, 2019-04, Vol.17 (1), p.138-138, Article 138

2019

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Effects of online continuing medical education on perspectives of shared decision-making among Chinese endocrinologists

BMC medical education, 2023-11, Vol.23 (1), p.1-878, Article 878

2023

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Identification of mutations in the prostaglandin transporter gene SLCO2A1 and phenotypic comparison between two subtypes of primary hypertrophic osteoarthropathy (PHO): A single-center study

Bone (New York, N.Y.), 2018-01, Vol.106, p.96-102

2018

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Improvement of Bone Health and Initiation of Puberty Development in Camurati-Engelmann Disease With Glucocorticoid and Losartan Treatment: A Case Report and Review of Literature

Frontiers in endocrinology (Lausanne), 2022-06, Vol.13, p.882144-882144

2022

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The first case report of Kyphoscoliotic Ehlers-Danlos syndrome of chinese origin with a novel PLOD1 gene mutation

BMC medical genetics, 2020-10, Vol.21 (1), p.214-214, Article 214

2020

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Myostatin regulates glucose metabolism via the AMP-activated protein kinase pathway in skeletal muscle cells

The international journal of biochemistry & cell biology, 2010-12, Vol.42 (12), p.2072-2081

2010

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EFFICACY AND SAFETY OF BISPHOSPHONATE THERAPY IN MCCUNE-ALBRIGHT SYNDROME-RELATED POLYOSTOTIC FIBROUS DYSPLASIA: A SINGLE-CENTER EXPERIENCE

Endocrine practice, 2019-01, Vol.25 (1), p.23-30

2019

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Using preoperative ultrasound vascularity characteristics to estimate medullary thyroid cancer

Cancer imaging, 2023-06, Vol.23 (1), p.64-64, Article 64

2023

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Clinical and genetic analysis of atypical parathyroid adenoma compared with parathyroid carcinoma and benign lesions in a Chinese cohort

Frontiers in endocrinology (Lausanne), 2023-01, Vol.14, p.1027598-1027598

2023

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Cardiovascular abnormalities and its correlation with genotypes of children with osteogenesis imperfecta

Frontiers in endocrinology (Lausanne), 2022-10, Vol.13, p.1004946-1004946

2022

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FGF23 and Phosphate Wasting Disorders

Bone research, 2013-06, Vol.1 (2), p.120-132

2013

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Disruption of FLNB leads to skeletal malformation by interfering with skeletal segmentation through the HOX gene

Bone Reports, 2024-03, Vol.20, p.101746-101746, Article 101746

2024

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The preliminary study on cardiac structure and function in Chinese patients with primary hyperparathyroidism

Frontiers in endocrinology (Lausanne), 2023-02, Vol.14, p.1083521-1083521

2023

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Associations of different dietary patterns, bone mineral density, and fracture risk among elderly women: the China Osteoporosis Prevalence Study

Frontiers in endocrinology (Lausanne), 2024-06, Vol.15, p.1378158

2024

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Locoregional recurrence of parathyroid carcinoma : how to identify this rare but fatal condition using ultrasonography

ENDOCRINE JOURNAL, 2021, Vol.68 (10), p.1179-1186

2021

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Cushing's Syndrome With Nocardiosis: A Case Report and a Systematic Review of the Literature

Frontiers in endocrinology (Lausanne), 2021-03, Vol.12, p.640998-640998

2021

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Clinical characteristics and the influence of rs1800470 in patients with Camurati-Engelmann disease

Frontiers in endocrinology (Lausanne), 2022-10, Vol.13, p.1041061-1041061

2022

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Health-related quality of life in men with osteoporosis: a systematic review and meta-analysis

The epidemiology of osteoporosis, associated fragility fractures, and management gap in China

A Chinese case of CHST3-related skeletal dysplasia and a systematic review

Shear wave elastography for differentiating parathyroid neoplasms with malignant diagnosis or uncertain malignant potential from parathyroid adenomas: initial experience

Novel AQP2 Mutations and Clinical Characteristics in Seven Chinese Families With Congenital Nephrogenic Diabetes Insipidus

Associations between FGF21, osteonectin and bone turnover markers in type 2 diabetic patients with albuminuria

Early bone loss in patients with obstructive sleep apnea: a cross-sectional study

Chinese bone turnover marker study: reference ranges for C-terminal telopeptide of type I collagen and procollagen I N-terminal peptide by age and gender

A 105 kb interstitial insertion in the Xq27.1 palindrome from pseudoautosomal region PAR1 causes a novel X-linked recessive compound phenotype

Effects of online continuing medical education on perspectives of shared decision-making among Chinese endocrinologists

Identification of mutations in the prostaglandin transporter gene SLCO2A1 and phenotypic comparison between two subtypes of primary hypertrophic osteoarthropathy (PHO): A single-center study

Improvement of Bone Health and Initiation of Puberty Development in Camurati-Engelmann Disease With Glucocorticoid and Losartan Treatment: A Case Report and Review of Literature

The first case report of Kyphoscoliotic Ehlers-Danlos syndrome of chinese origin with a novel PLOD1 gene mutation

Myostatin regulates glucose metabolism via the AMP-activated protein kinase pathway in skeletal muscle cells

EFFICACY AND SAFETY OF BISPHOSPHONATE THERAPY IN MCCUNE-ALBRIGHT SYNDROME-RELATED POLYOSTOTIC FIBROUS DYSPLASIA: A SINGLE-CENTER EXPERIENCE

Using preoperative ultrasound vascularity characteristics to estimate medullary thyroid cancer

Clinical and genetic analysis of atypical parathyroid adenoma compared with parathyroid carcinoma and benign lesions in a Chinese cohort

Cardiovascular abnormalities and its correlation with genotypes of children with osteogenesis imperfecta

FGF23 and Phosphate Wasting Disorders

Disruption of FLNB leads to skeletal malformation by interfering with skeletal segmentation through the HOX gene

The preliminary study on cardiac structure and function in Chinese patients with primary hyperparathyroidism

Associations of different dietary patterns, bone mineral density, and fracture risk among elderly women: the China Osteoporosis Prevalence Study

Locoregional recurrence of parathyroid carcinoma : how to identify this rare but fatal condition using ultrasonography

Cushing's Syndrome With Nocardiosis: A Case Report and a Systematic Review of the Literature

Clinical characteristics and the influence of rs1800470 in patients with Camurati-Engelmann disease

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