Ozono K - Search Results

1

Diagnostic delay is common among patients with hypophosphatasia: initial findings from a longitudinal, prospective, global registry.

Högler W, Langman C, Gomes da Silva H, Fang S, Linglart A, Ozono K, Petryk A, Rockman-Greenberg C, Seefried L, Kishnani PS. Högler W, et al. Among authors: ozono k. BMC Musculoskelet Disord. 2019 Feb 14;20(1):80. doi: 10.1186/s12891-019-2420-8. BMC Musculoskelet Disord. 2019. PMID: 30764793 Free PMC article.

2

Identification of novel missense mutations (Phe310Leu and Gly439Arg) in a neonatal case of hypophosphatasia.

Ozono K, Yamagata M, Michigami T, Nakajima S, Sakai N, Cai G, Satomura K, Yasui N, Okada S, Nakayama M. Ozono K, et al. J Clin Endocrinol Metab. 1996 Dec;81(12):4458-61. doi: 10.1210/jcem.81.12.8954059. J Clin Endocrinol Metab. 1996. PMID: 8954059

3

[Hypophosphatasia].

Ozono K, Cai G. Ozono K, et al. Ryoikibetsu Shokogun Shirizu. 1998;(19 Pt 2):669-72. Ryoikibetsu Shokogun Shirizu. 1998. PMID: 9645163 Review. Japanese. No abstract available.

4

Asp361Val Mutant of alkaline phosphatase found in patients with dominantly inherited hypophosphatasia inhibits the activity of the wild-type enzyme.

Müller HL, Yamazaki M, Michigami T, Kageyama T, Schönau E, Schneider P, Ozono K. Müller HL, et al. Among authors: ozono k. J Clin Endocrinol Metab. 2000 Feb;85(2):743-7. doi: 10.1210/jcem.85.2.6373. J Clin Endocrinol Metab. 2000. PMID: 10690885

5

[Therapy for hypophosphatasia].

Ozono K. Ozono K. Clin Calcium. 2007 Oct;17(10):1600-6. Clin Calcium. 2007. PMID: 17906415 Review. Japanese.

6

[Enzyme replacement therapy for hypophosphatasia].

Ozono K. Ozono K. Clin Calcium. 2014 Feb;24(2):257-63. Clin Calcium. 2014. PMID: 24473359 Review. Japanese.

7

Asfotase Alfa Treatment Improves Survival for Perinatal and Infantile Hypophosphatasia.

Whyte MP, Rockman-Greenberg C, Ozono K, Riese R, Moseley S, Melian A, Thompson DD, Bishop N, Hofmann C. Whyte MP, et al. Among authors: ozono k. J Clin Endocrinol Metab. 2016 Jan;101(1):334-42. doi: 10.1210/jc.2015-3462. Epub 2015 Nov 3. J Clin Endocrinol Metab. 2016. PMID: 26529632 Free PMC article. Clinical Trial.

8

Monitoring guidance for patients with hypophosphatasia treated with asfotase alfa.

Kishnani PS, Rush ET, Arundel P, Bishop N, Dahir K, Fraser W, Harmatz P, Linglart A, Munns CF, Nunes ME, Saal HM, Seefried L, Ozono K. Kishnani PS, et al. Among authors: ozono k. Mol Genet Metab. 2017 Sep;122(1-2):4-17. doi: 10.1016/j.ymgme.2017.07.010. Epub 2017 Jul 25. Mol Genet Metab. 2017. PMID: 28888853 Free article. Review.

9

Adult hypophosphatasia with compound heterozygous p.Phe327Leu missense and c.1559delT frameshift mutations in tissue-nonspecific alkaline phosphatase gene: a case report.

Fukushima K, Kawai-Kowase K, Yonemoto Y, Fujiwara M, Sato H, Sato M, Kubota T, Ozono K, Tamura J. Fukushima K, et al. Among authors: ozono k. J Med Case Rep. 2019 Apr 24;13(1):101. doi: 10.1186/s13256-019-2045-4. J Med Case Rep. 2019. PMID: 31014398 Free PMC article.

10

Japanese nationwide survey of hypophosphatasia reveals prominent differences in genetic and dental findings between odonto and non-odonto types.

Okawa R, Kokomoto K, Kitaoka T, Kubota T, Watanabe A, Taketani T, Michigami T, Ozono K, Nakano K. Okawa R, et al. Among authors: ozono k. PLoS One. 2019 Oct 10;14(10):e0222931. doi: 10.1371/journal.pone.0222931. eCollection 2019. PLoS One. 2019. PMID: 31600233 Free PMC article.

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