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ArticlesPeer ReviewedFull Text
X-Linked Hypophosphatemia Transition and Team Management
Author / Creator:Kubota, Takuo
Publisher:Basel: MDPI AG
Journal title:Endocrines, 2022-09, Vol.3 (3), p.411-418
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Prevalence of Pseudohypoparathyroidism and Nonsurgical Hypoparathyroidism in Japan in 2017: A Nationwide Survey
Author / Creator:Takatani, Rieko ; Kubota, Takuo ; Minagawa, Masanori ; Inoue, Daisuke ; Fukumoto, Seiji ; Ozono, Keiichi ; Nakamura, Yosikazu
Publisher:Japan Epidemiological Association
Journal title:Journal of Epidemiology, 2023/11/05, Vol.33(11), pp.569-573
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Hypophosphatasia in Japan: ALPL Mutation Analysis in 98 Unrelated Patients
Author / Creator:Michigami, Toshimi ; Tachikawa, Kanako ; Yamazaki, Miwa ; Kawai, Masanobu ; Kubota, Takuo ; Ozono, Keiichi
Publisher:New York: Springer US
Journal title:Calcified tissue international, 2020-03, Vol.106 (3), p.221-231
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Wnt signaling in bone metabolism
Author / Creator:Kubota, Takuo ; Michigami, Toshimi ; Ozono, Keiichi
Publisher:Japan: Japan : Springer Japan
Journal title:Journal of bone and mineral metabolism, 2009-05, Vol.27 (3), p.265-271
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Japanese nationwide dental survey of hypophosphatasia reveals novel oral manifestations
Author / Creator:Okawa, Rena ; Kadota, Tamami ; Kurosaka, Hiroshi ; Nakayama, Hirofumi ; Ochiai, Marin ; Ogaya, Yuko ; Kubota, Takuo ; Yamashiro, Takashi ; Nakano, Kazuhiko
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2025-02, Vol.15 (1), p.6743-12, Article 6743
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Incidence rate of vitamin D deficiency and FGF23 levels in 12- to 13-year-old adolescents in Japan
Author / Creator:Koyama, Satomi ; Kubota, Takuo ; Naganuma, Junko ; Arisaka, Osamu ; Ozono, Keiichi ; Yoshihara, Shigemi
Publisher:Singapore: Springer Singapore
Journal title:Journal of bone and mineral metabolism, 2021-05, Vol.39 (3), p.456-462
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Japanese nationwide survey of hypophosphatasia reveals prominent differences in genetic and dental findings between odonto and non-odonto types
Author / Creator:Okawa, Rena ; Kokomoto, Kazuma ; Kitaoka, Taichi ; Kubota, Takuo ; Watanabe, Atsushi ; Taketani, Takeshi ; Michigami, Toshimi ; Ozono, Keiichi ; Nakano, Kazuhiko
Publisher:United States: Public Library of Science
Journal title:PloS one, 2019-10, Vol.14 (10), p.e0222931-e0222931
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Association of trabecular bone score and bone mineral apparent density with the severity of bone fragility in children and adolescents with osteogenesis imperfecta: A cross-sectional study
Author / Creator:Ohata, Yasuhisa ; Kitaoka, Taichi ; Ishimi, Takeshi ; Yamada, Chieko ; Nakano, Yukako ; Yamamoto, Kenichi ; Takeyari, Shinji ; Nakayama, Hirofumi ; Fujiwara, Makoto ; Kubota, Takuo ; Ozono, Keiichi
Publisher:San Francisco: Public Library of Science
Journal title:PloS one, 2023-08, Vol.18 (8), p.e0290812-e0290812
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Clinical performance of a novel chemiluminescent enzyme immunoassay for FGF23
Author / Creator:Ito, Nobuaki ; Kubota, Takuo ; Kitanaka, Sachiko ; Fujiwara, Ikuma ; Adachi, Masanori ; Takeuchi, Yasuhiro ; Yamagami, Hitomi ; Kimura, Takehide ; Shinoda, Tatsuya ; Minagawa, Masanori ; Okazaki, Ryo ; Ozono, Keiichi ; Seino, Yoshiki ; Fukumoto, Seiji
Publisher:Singapore: Springer Singapore
Journal title:Journal of bone and mineral metabolism, 2021-11, Vol.39 (6), p.1066-1075
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An overgrowth disorder associated with excessive production of cGMP due to a gain-of-function mutation of the natriuretic peptide receptor 2 gene
Author / Creator:Miura, Kohji ; Namba, Noriyuki ; Fujiwara, Makoto ; Ohata, Yasuhisa ; Ishida, Hidekazu ; Kitaoka, Taichi ; Kubota, Takuo ; Hirai, Haruhiko ; Higuchi, Chikahisa ; Tsumaki, Noriyuki ; Yoshikawa, Hideki ; Sakai, Norio ; Michigami, Toshimi ; Ozono, Keiichi
Publisher:United States: Public Library of Science
Journal title:PloS one, 2012-08, Vol.7 (8), p.e42180
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Impact of fracture characteristics and disease-specific complications on health-related quality of life in osteogenesis imperfecta
Author / Creator:Matsushita, Masaki ; Mishima, Kenichi ; Yamashita, Satoshi ; Haga, Nobuhiko ; Fujiwara, Sayaka ; Ozono, Keiichi ; Kubota, Takuo ; Kitaoka, Taichi ; Ishiguro, Naoki ; Kitoh, Hiroshi
Publisher:Tokyo: Springer Japan
Journal title:Journal of bone and mineral metabolism, 2020-01, Vol.38 (1), p.109-116
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The 2023 Guidelines for the management and treatment of glucocorticoid-induced osteoporosis
Author / Creator:Tanaka, Yoshiya ; Soen, Satoshi ; Hirata, Shintaro ; Okada, Yosuke ; Fujiwara, Saeko ; Tanaka, Ikuko ; Kitajima, Yuriko ; Kubota, Takuo ; Ebina, Kosuke ; Takashi, Yuichi ; Inoue, Reiko ; Yamauchi, Mika ; Okubo, Naoaki ; Ueno, Masanobu ; Ohata, Yasuhisa ; Ito, Nobuaki ; Ozono, Keiichi ; Nakayama, Hisanori ; Terauchi, Masakazu ; Tanaka, Sakae ; Fukumoto, Seiji
Publisher:Singapore: Springer Nature Singapore
Journal title:Journal of bone and mineral metabolism, 2024-03, Vol.42 (2), p.143-154
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Development of scoliosis in young children with osteogenesis imperfecta undergoing intravenous bisphosphonate therapy
Author / Creator:Kashii, Masafumi ; Kanayama, Sadaaki ; Kitaoka, Taichi ; Makino, Takahiro ; Kaito, Takashi ; Iwasaki, Motoki ; Kubota, Takuo ; Yamamoto, Takehisa ; Ozono, Keiichi ; Yoshikawa, Hideki
Publisher:Tokyo: Springer Japan
Journal title:Journal of bone and mineral metabolism, 2019-05, Vol.37 (3), p.545-553
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Long-term outcomes for Asian patients with X-linked hypophosphataemia: rationale and design of the SUNFLOWER longitudinal, observational cohort study
Author / Creator:Kubota, Takuo ; Fukumoto, Seiji ; Cheong, Hae Il ; Michigami, Toshimi ; Namba, Noriyuki ; Ito, Nobuaki ; Tokunaga, Shin ; Gibbs, Yoshimi ; Ozono, Keiichi
Publisher:England: BMJ Publishing Group LTD
Journal title:BMJ open, 2020-06, Vol.10 (6), p.e036367
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Burosumab treatment in adults with X-linked hypophosphataemia: 96-week patient-reported outcomes and ambulatory function from a randomised phase 3 trial and open-label extension
Author / Creator:Briot, Karine ; Portale, Anthony A ; Brandi, Maria Luisa ; Carpenter, Thomas O ; Cheong, Hae Ii ; Cohen-Solal, Martine ; Crowley, Rachel K ; Eastell, Richard ; Imanishi, Yasuo ; Ing, Steven ; Insogna, Karl ; Ito, Nobuaki ; Jan de Beur, Suzanne ; Javaid, Muhammad K ; Kamenicky, Peter ; Keen, Richard ; Kubota, Takuo ; Lachmann, Robin H ; Perwad, Farzana ; Pitukcheewanont, Pisit ; Ralston, Stuart H ; Takeuchi, Yasuhiro ; Tanaka, Hiroyuki ; Weber, Thomas J ; Yoo, Han-Wook ; Nixon, Annabel ; Nixon, Mark ; Sun, Wei ; Williams, Angela ; Imel, Erik A
Publisher:England: EULAR
Journal title:Rheumatic & musculoskeletal diseases open, 2021-09, Vol.7 (3), p.e001714
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Phenotypes of a family with XLH with a novel PHEX mutation
Author / Creator:Yamamoto, Akiko ; Nakamura, Toshiro ; Ohata, Yasuhisa ; Kubota, Takuo ; Ozono, Keiichi
Publisher:London: Nature Publishing Group UK
Journal title:Human genome variation, 2020-03, Vol.7 (1), p.8-8, Article 8
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Adult hypophosphatasia with compound heterozygous p.Phe327Leu missense and c.1559delT frameshift mutations in tissue-nonspecific alkaline phosphatase gene: a case report
Author / Creator:Fukushima, Kazunori ; Kawai-Kowase, Keiko ; Yonemoto, Yukio ; Fujiwara, Makoto ; Sato, Hiroko ; Sato, Mahito ; Kubota, Takuo ; Ozono, Keiichi ; Tamura, Junich
Publisher:England: BioMed Central Ltd
Journal title:Journal of medical case reports, 2019-04, Vol.13 (1), p.101-101, Article 101
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A novel PTCH1 mutation in basal cell nevus syndrome with rare craniofacial features
Author / Creator:Murata, Yuka ; Kurosaka, Hiroshi ; Ohata, Yasuhisa ; Aikawa, Tomonao ; Takahata, Sosuke ; Fujii, Katsunori ; Miyashita, Toshiyuki ; Morita, Chisato ; Inubushi, Toshihiro ; Kubota, Takuo ; Sakai, Norio ; Ozono, Keiichi ; Kogo, Mikihiko ; Yamashiro, Takashi
Publisher:London: Nature Publishing Group UK
Journal title:Human genome variation, 2019-04, Vol.6 (1), p.16-16, Article 16
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Decrease in serum FGF23 levels after intravenous infusion of pamidronate in patients with osteogenesis imperfecta
Author / Creator:Kitaoka, Taichi ; Namba, Noriyuki ; Miura, Kohji ; Kubota, Takuo ; Ohata, Yasuhisa ; Fujiwara, Makoto ; Hirai, Haruhiko ; Yamamoto, Takehisa ; Ozono, Keiichi
Publisher:Japan: Springer Japan
Journal title:Journal of bone and mineral metabolism, 2011-09, Vol.29 (5), p.598-605
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Serum Fibroblast Growth Factor 23 Is a Useful Marker to Distinguish Vitamin D-Deficient Rickets from Hypophosphatemic Rickets
Author / Creator:Kubota, Takuo ; Kitaoka, Taichi ; Miura, Kohji ; Fujiwara, Makoto ; Ohata, Yasuhisa ; Miyoshi, Yoko ; Yamamoto, Keiko ; Takeyari, Shinji ; Yamamoto, Takehisa ; Namba, Noriyuki ; Ozono, Keiichi
Publisher:Basel, Switzerland: S. Karger AG
Journal title:Hormone research in paediatrics, 2014-01, Vol.81 (4), p.251-257
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Showing 1 to 20 of 33 results

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X-Linked Hypophosphatemia Transition and Team Management

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Prevalence of Pseudohypoparathyroidism and Nonsurgical Hypoparathyroidism in Japan in 2017: A Nationwide Survey

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Hypophosphatasia in Japan: ALPL Mutation Analysis in 98 Unrelated Patients

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Wnt signaling in bone metabolism

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Japanese nationwide dental survey of hypophosphatasia reveals novel oral manifestations

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Incidence rate of vitamin D deficiency and FGF23 levels in 12- to 13-year-old adolescents in Japan

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

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Association of trabecular bone score and bone mineral apparent density with the severity of bone fragility in children and adolescents with osteogenesis imperfecta: A cross-sectional study

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Clinical performance of a novel chemiluminescent enzyme immunoassay for FGF23

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

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Impact of fracture characteristics and disease-specific complications on health-related quality of life in osteogenesis imperfecta

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The 2023 Guidelines for the management and treatment of glucocorticoid-induced osteoporosis

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Development of scoliosis in young children with osteogenesis imperfecta undergoing intravenous bisphosphonate therapy

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Long-term outcomes for Asian patients with X-linked hypophosphataemia: rationale and design of the SUNFLOWER longitudinal, observational cohort study

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Burosumab treatment in adults with X-linked hypophosphataemia: 96-week patient-reported outcomes and ambulatory function from a randomised phase 3 trial and open-label extension

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Phenotypes of a family with XLH with a novel PHEX mutation

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

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A novel PTCH1 mutation in basal cell nevus syndrome with rare craniofacial features

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

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Serum Fibroblast Growth Factor 23 Is a Useful Marker to Distinguish Vitamin D-Deficient Rickets from Hypophosphatemic Rickets

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