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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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Widespread Transcriptional Scanning in the Testis Modulates Gene Evolution Rates

Cell, 2020-01, Vol.180 (2), p.248-262.e21

2020

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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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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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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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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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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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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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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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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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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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H7N9 Influenza A-induced Pneumonia Associated with Acute Myelitis in an Adult

Internal Medicine, 2014, Vol.53(10), pp.1093-1095

2014

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Comparison of Implantable Collamer Lens Visian ICL V4 and ICL V4c for high myopia: A cohort study

Medicine (Baltimore), 2017-06, Vol.96 (25), p.e7294-e7294

2017

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Low-dose adefovir dipivoxil may induce Fanconi syndrome: clinical characteristics and long-term follow-up for Chinese patients

Antiviral therapy, 2015-01, Vol.20 (6), p.603-611

2015

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Changes in Serum Calcium and Treatment of Hypoparathyroidism During Pregnancy and Lactation: A Single-center Case Series

The journal of clinical endocrinology and metabolism, 2021-12, Vol.106 (12), p.e5054-e5063

2021

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A Common Mutation and a Novel Mutation in the HPGD Gene in Nine Patients with Primary Hypertrophic Osteoarthropathy

Calcified tissue international, 2015-10, Vol.97 (4), p.336-342

2015

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Levels and dynamic changes of serum fibroblast growth factor 23 in hypophosphatemic rickets/osteomalacia

Chinese medical journal, 2010-05, Vol.123 (9), p.1158-1162

2010

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A "blind" vascular ring in association with congenital cystic adenomatoid malformation: A case report

Medicine (Baltimore), 2017-12, Vol.96 (51), p.e8915-e8915

2017

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Oxaliplatin and 5-fluorouracil hepatic infusion with lipiodolized chemoembolization in large hepatocellular carcinoma

World journal of gastroenterology : WJG, 2015-04, Vol.21 (13), p.3970-3977

2015

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Long term efficacy of minimal incision osteotomy for hallux abducto valgus

Orthopaedic surgery, 2010-08, Vol.2 (3), p.223-228

2010

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SOST polymorphisms and response to alendronate treatment in postmenopausal Chinese women with osteoporosis

Pharmacogenomics, 2015-07, Vol.16 (10), p.1077-1088

2015

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THE CLINICAL CHARACTERISTICS AND EFFICACY OF BISPHOSPHONATES IN AUDLT PATIENTS WITH OSTEOGENESIS IMPERGECTA

Endocrine practice, 2016-11, Vol.22 (11), p.1267-1276

2016

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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

Widespread Transcriptional Scanning in the Testis Modulates Gene Evolution Rates

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

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

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

Mitochondrial DNA hypomethylation in chrome plating workers

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

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

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

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

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

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

H7N9 Influenza A-induced Pneumonia Associated with Acute Myelitis in an Adult

Comparison of Implantable Collamer Lens Visian ICL V4 and ICL V4c for high myopia: A cohort study

Low-dose adefovir dipivoxil may induce Fanconi syndrome: clinical characteristics and long-term follow-up for Chinese patients

Changes in Serum Calcium and Treatment of Hypoparathyroidism During Pregnancy and Lactation: A Single-center Case Series

A Common Mutation and a Novel Mutation in the HPGD Gene in Nine Patients with Primary Hypertrophic Osteoarthropathy

Levels and dynamic changes of serum fibroblast growth factor 23 in hypophosphatemic rickets/osteomalacia

A "blind" vascular ring in association with congenital cystic adenomatoid malformation: A case report

Oxaliplatin and 5-fluorouracil hepatic infusion with lipiodolized chemoembolization in large hepatocellular carcinoma

Long term efficacy of minimal incision osteotomy for hallux abducto valgus

SOST polymorphisms and response to alendronate treatment in postmenopausal Chinese women with osteoporosis

THE CLINICAL CHARACTERISTICS AND EFFICACY OF BISPHOSPHONATES IN AUDLT PATIENTS WITH OSTEOGENESIS IMPERGECTA

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