29 results on '"Ozono, Keiichi"'
Search Results
2. Clinical performance of a novel chemiluminescent enzyme immunoassay for FGF23
3. Incidence rate of vitamin D deficiency and FGF23 levels in 12- to 13-year-old adolescents in Japan
4. Impact of fracture characteristics and disease-specific complications on health-related quality of life in osteogenesis imperfecta
5. Development of scoliosis in young children with osteogenesis imperfecta undergoing intravenous bisphosphonate therapy
6. Assessment criteria for vitamin D deficiency/insufficiency in Japan: proposal by an expert panel supported by the Research Program of Intractable Diseases, Ministry of Health, Labour and Welfare, Japan, the Japanese Society for Bone and Mineral Research and the Japan Endocrine Society [Opinion]
7. Pathogenesis and diagnostic criteria for rickets and osteomalacia—proposal by an expert panel supported by the Ministry of Health, Labour and Welfare, Japan, the Japanese Society for Bone and Mineral Research, and the Japan Endocrine Society
8. Interleukin-1-induced acute bone resorption facilitates the secretion of fibroblast growth factor 23 into the circulation
9. Guidelines on the management and treatment of glucocorticoid-induced osteoporosis of the Japanese Society for Bone and Mineral Research: 2014 update
10. Decrease in serum FGF23 levels after intravenous infusion of pamidronate in patients with osteogenesis imperfecta
11. Wnt signaling in bone metabolism
12. Hereditary hypophosphatemic rickets with hypercalciuria: a study for the phosphate transporter gene type IIc and osteoblastic function
13. Genetic association of a polymorphism of the cAMP-responsive element binding protein-binding protein with steroid-induced osteonecrosis after kidney transplantation
14. The role of fibroblast growth factor 23 for hypophosphatemia and abnormal regulation of vitamin D metabolism in patients with McCune–Albright syndrome
15. Long-term hospitalization during pregnancy is a risk factor for vitamin D deficiency in neonates
16. Alendronate and pharmacological doses of 1α OHD3 therapy in a patient with McCune-Albright syndrome and accompanying hypophosphatemia
17. Hypophosphatemic rickets accompanying McCune–Albright syndrome: evidence that a humoral factor causes hypophosphatemia
18. Treatment with recombinant IL-2 for recurrent respiratory infection in a case of cartilage-hair hypoplasia with autoimmune hemolytic anemia
19. Analysis of the stable levels of messenger RNA derived from different polymorphic alleles in the vitamin D receptor gene
20. Incidence rate of vitamin D deficiency and FGF23 levels in 12- to 13-year-old adolescents in Japan
21. The role of IGF-I in phosphate therapy for the short stature of patients with hypophosphatemic vitamin D-resistant rickets
22. Impact of fracture characteristics and disease-specific complications on health-related quality of life in osteogenesis imperfecta
23. Development of scoliosis in young children with osteogenesis imperfecta undergoing intravenous bisphosphonate therapy
24. Assessment criteria for vitamin D deficiency/insufficiency in Japan: proposal by an expert panel supported by the Research Program of Intractable Diseases, Ministry of Health, Labour and Welfare, Japan, the Japanese Society for Bone and Mineral Research and the Japan Endocrine Society [Opinion]
25. Interleukin-1-induced acute bone resorption facilitates the secretion of fibroblast growth factor 23 into the circulation
26. The role of fibroblast growth factor 23 for hypophosphatemia and abnormal regulation of vitamin D metabolism in patients with McCune?Albright syndrome
27. Alendronate and pharmacological doses of 1à OHD 3 therapy in a patient with McCune-Albright syndrome and accompanying hypophosphatemia
28. Hypophosphatemic rickets accompanying McCune?Albright syndrome: evidence that a humoral factor causes hypophosphatemia
29. Alendronate and pharmacological doses of 1α OHD3 therapy in a patient with McCune-Albright syndrome and accompanying hypophosphatemia
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