Fujiwara M - Search Results

1

Clinical Practice Guidelines for Hypophosphatasia.

Michigami T, Ohata Y, Fujiwara M, Mochizuki H, Adachi M, Kitaoka T, Kubota T, Sawai H, Namba N, Hasegawa K, Fujiwara I, Ozono K. Michigami T, et al. Among authors: fujiwara i, fujiwara m. Clin Pediatr Endocrinol. 2020;29(1):9-24. doi: 10.1297/cpe.29.9. Epub 2020 Jan 9. Clin Pediatr Endocrinol. 2020. PMID: 32029969 Free PMC article.

2

Decrease in serum FGF23 levels after intravenous infusion of pamidronate in patients with osteogenesis imperfecta.

Kitaoka T, Namba N, Miura K, Kubota T, Ohata Y, Fujiwara M, Hirai H, Yamamoto T, Ozono K. Kitaoka T, et al. Among authors: fujiwara m. J Bone Miner Metab. 2011 Sep;29(5):598-605. doi: 10.1007/s00774-011-0262-z. Epub 2011 Feb 23. J Bone Miner Metab. 2011. PMID: 21344299 Clinical Trial.

3

Monocarboxylate transporter 10 functions as a thyroid hormone transporter in chondrocytes.

Abe S, Namba N, Abe M, Fujiwara M, Aikawa T, Kogo M, Ozono K. Abe S, et al. Among authors: fujiwara m. Endocrinology. 2012 Aug;153(8):4049-58. doi: 10.1210/en.2011-1713. Epub 2012 Jun 19. Endocrinology. 2012. PMID: 22719050

4

An overgrowth disorder associated with excessive production of cGMP due to a gain-of-function mutation of the natriuretic peptide receptor 2 gene.

Miura K, Namba N, Fujiwara M, Ohata Y, Ishida H, Kitaoka T, Kubota T, Hirai H, Higuchi C, Tsumaki N, Yoshikawa H, Sakai N, Michigami T, Ozono K. Miura K, et al. Among authors: fujiwara m. PLoS One. 2012;7(8):e42180. doi: 10.1371/journal.pone.0042180. Epub 2012 Aug 3. PLoS One. 2012. PMID: 22870295 Free PMC article. Clinical Trial.

5

Pediatric aspects of skeletal dysplasia.

Ozono K, Namba N, Kubota T, Kitaoka T, Miura K, Ohata Y, Fujiwara M, Miyoshi Y, Michigami T. Ozono K, et al. Among authors: fujiwara m. Pediatr Endocrinol Rev. 2012 Oct;10 Suppl 1:35-43. Pediatr Endocrinol Rev. 2012. PMID: 23330244 Review.

6

Detection and characterization of two novel mutations in the HNF4A gene in maturity-onset diabetes of the young type 1 in two Japanese families.

Fujiwara M, Namba N, Miura K, Kitaoka T, Hirai H, Kondou H, Shimotsuji T, Numakura C, Ozono K. Fujiwara M, et al. Horm Res Paediatr. 2013;79(4):220-6. doi: 10.1159/000350520. Epub 2013 May 1. Horm Res Paediatr. 2013. PMID: 23652628

7

Treatment of Hypophosphatemic Rickets with Phosphate and Active Vitamin D in Japan: A Questionnaire-based Survey.

Fujiwara M, Namba N, Ozono K, Arisaka O, Yokoya S; Committee on Drugs, Japanese Society for Pediatric Endocrinology*. Fujiwara M, et al. Clin Pediatr Endocrinol. 2013 Jan;22(1):9-14. doi: 10.1292/cpe.22.. Epub 2013 Feb 7. Clin Pediatr Endocrinol. 2013. PMID: 23966755 Free PMC article.

8

Two Japanese familial cases of Caffey disease with and without the common COL1A1 mutation and normal bone density, and review of the literature.

Kitaoka T, Miyoshi Y, Namba N, Miura K, Kubota T, Ohata Y, Fujiwara M, Takagi M, Hasegawa T, Jüppner H, Ozono K. Kitaoka T, et al. Among authors: fujiwara m. Eur J Pediatr. 2014 Jun;173(6):799-804. doi: 10.1007/s00431-013-2252-8. Epub 2014 Jan 4. Eur J Pediatr. 2014. PMID: 24390061 Review.

9

Serum fibroblast growth factor 23 is a useful marker to distinguish vitamin D-deficient rickets from hypophosphatemic rickets.

Kubota T, Kitaoka T, Miura K, Fujiwara M, Ohata Y, Miyoshi Y, Yamamoto K, Takeyari S, Yamamoto T, Namba N, Ozono K. Kubota T, et al. Among authors: fujiwara m. Horm Res Paediatr. 2014;81(4):251-7. doi: 10.1159/000357142. Epub 2014 Feb 26. Horm Res Paediatr. 2014. PMID: 24577200

10

[Cytokines and osteogenesis].

Fujiwara M, Ozono K. Fujiwara M, et al. Clin Calcium. 2014 Jun;24(6):845-51. Clin Calcium. 2014. PMID: 24870835 Review. Japanese.

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