253 results on '"Xia, Wei-Bo"'
Search Results
2. Health-related quality of life of men with primary osteoporosis and its changes after bisphosphonates treatment
3. Opening pattern of key laboratory improves the innovation ability of medical students
4. Specific Characteristic of Hyperplastic Callus in a Larger Cohort of Osteogenesis Imperfecta Type V
5. Efficacy of Yigu® versus Aclasta® in Chinese postmenopausal women with osteoporosis: a multicenter prospective study
6. Effects of Bisphosphonates on Osteoporosis Induced by Duchenne Muscular Dystrophy: A Prospective Study
7. Characterization of the clinical and genetic spectrum of autoimmune polyendocrine syndrome type 1 in Chinese case series
8. Effects of zoledronic acid on vertebral shape of children and adolescents with osteogenesis imperfecta
9. Safety and efficacy of cyclooxygenase-2 inhibition for treatment of primary hypertrophic osteoarthropathy: A single-arm intervention trial
10. Clinical characteristics and bisphosphonates treatment of rare pregnancy- and lactation-associated osteoporosis
11. Incidence and cost of vertebral fracture in urban China: A five-year population-based cohort study
12. Impaired bone strength and bone microstructure in a novel early-onset osteoporotic rat model with a clinically relevant PLS3 mutation
13. Global guidance for the recognition, diagnosis, and management of tumor-induced osteomalacia
14. Association Between Geranylgeranyl Pyrophosphate Synthase Gene Polymorphisms and Bone Phenotypes and Response to Alendronate Treatment in Chinese Osteoporotic Women
15. Primary hypertrophic osteoarthropathy related gastrointestinal complication has distinctive clinical and pathological characteristics: two cases report and review of the literature
16. Author response: Impaired bone strength and bone microstructure in a novel early-onset osteoporotic rat model with a clinically relevant PLS3 mutation
17. Novel mutations in FKBP10 in Chinese patients with osteogenesis imperfecta and their treatment with zoledronic acid
18. Novel Mutations in SERPINF1 Result in Rare Osteogenesis Imperfecta Type VI
19. Global guidance for the recognition, diagnosis, and management of tumor‐induced osteomalacia
20. Pseudohypoparathyroidism during pregnancy and the postpartum period: A case series of five patients
21. Clinical characteristics associated with bone mineral density improvement after 1-year alendronate/vitamin d3 or calcitriol treatment: Exploratory results from a phase 3, randomized, controlled trial on postmenopausal osteoporotic women in China
22. Calcifediol (25-hydroxyvitamin D) improvement and calcium-phosphate metabolism of alendronate sodium/vitamin D3 combination in Chinese women with postmenopausal osteoporosis: a post hoc efficacy analysis and safety reappraisal
23. Two novel mutations in TMEM38B result in rare autosomal recessive osteogenesis imperfecta
24. Gorham-Stout disease: radiological, histological, and clinical features of 12 cases and review of literature
25. The role of osteocalcin in regulation of glycolipid metabolism and muscle function in children with osteogenesis imperfecta
26. Impaired bone strength and bone microstructure in a novel early-onset osteoporotic rat model with a clinically relevant PLS3 mutation
27. A Common Mutation and a Novel Mutation in the HPGD Gene in Nine Patients with Primary Hypertrophic Osteoarthropathy
28. Risk factors of hyperparathyroidism in Chinese X-linked hypophosphatemia (XLH) patients: A cohort study
29. Effects of Bisphosphonates on Bone of Osteoporotic Men With Different Androgen Levels: A Case-Control Study
30. NFKB2 mutation in common variable immunodeficiency and isolated adrenocorticotropic hormone deficiency: A case report and review of literature
31. Changes in Serum Calcium and Treatment of Hypoparathyroidism During Pregnancy and Lactation: A Single-center Case Series
32. Infusion of ibandronate once every 3 months effectively decreases bone resorption markers and increases bone mineral density in Chinese postmenopausal osteoporotic women: a 1-year study
33. A novel homozygous mutation of the calcium-sensing receptor gene associated with apparent autosomal recessive inheritance of familial hypocalciuric hypercalcemia
34. Consensus on clinical management of tumor-induced osteomalacia
35. Expression of Ki-67, galectin-3, fragile histidine triad, and parafibromin in malignant and benign parathyroid tumors
36. Exome sequencing identifies compound heterozygous PKHD1 mutations as a cause of autosomal recessive polycystic kidney disease
37. Benefit of infusions with ibandronate treatment in children with osteogenesis imperfecta
38. A novel variant in AIRE causing a rare, non‑classical autoimmune polyendocrine syndrome type 1
39. Novel variants in COL2A1 causing rare spondyloepiphyseal dysplasia congenita
40. Levels and dynamic changes of serum fibroblast growth factor 23 in hypophosphatemic rickets/osteomalacia
41. Treatment of hypocalcemia caused by hypoparathyroidism or pseudohypoparathyroidism with domestic-made calcitriol: a prospective and self-controlled clinical trial
42. Vitamin D deficiency and osteoporosis
43. MOESM1 of Primary hypertrophic osteoarthropathy related gastrointestinal complication has distinctive clinical and pathological characteristics: two cases report and review of the literature
44. Effect of fibroblast growth factor 9 on Runx2 gene promoter activity in MC3T3-E1 and C2C12 cells
45. Changes in Serum Calcium and Treatment of Hypoparathyroidism During Pregnancy and Lactation: A Single-center Case Series.
46. Additional file 1: of Calcifediol (25-hydroxyvitamin D) improvement and calcium-phosphate metabolism of alendronate sodium/vitamin D3 combination in Chinese women with postmenopausal osteoporosis: a post hoc efficacy analysis and safety reappraisal
47. Ring sign: an imaging sign for osteochondromyxoma in Carney complex
48. Genotype-phenotype relationship in a large cohort of osteogenesis imperfecta patients with COL1A1 mutations revealed by a new scoring system
49. Extremely low level of serum pigment epithelium-derived factor is a special biomarker of Chinese osteogenesis imperfecta patients with SERPINF1 mutations
50. A Novel De novo GATA-binding Protein 3 Mutation in a Patient with Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia Syndrome
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.