Clinical Practice Guidelines for Hypophosphatasia*-Reference-Cited by-同舟云学术

Clinical Practice Guidelines for Hypophosphatasia*

Published:2020 Issue:1 Volume:29 Page:9-24
ISSN:0918-5739
Container-title:Clinical Pediatric Endocrinology
language:en
Short-container-title:Clin Pediatr Endocrinol

Author:

Michigami Toshimi¹²,Ohata Yasuhisa³²,Fujiwara Makoto³²,Mochizuki Hiroshi⁴²,Adachi Masanori⁵²,Kitaoka Taichi³²,Kubota Takuo³²,Sawai Hideaki⁶²,Namba Noriyuki⁷²,Hasegawa Kosei⁸²,Fujiwara Ikuma⁹²,Ozono Keiichi³²

Affiliation:

1. Department of Bone and Mineral Research, Research Institute, Osaka Women’s and Children’s Hospital, Osaka Prefectural Hospital Organization, Osaka, Japan

2. Task Force for Hypophosphatasia Guidelines

3. Department of Pediatrics, Osaka University Graduate School of Medicine, Osaka, Japan

4. Division of Endocrinology and Metabolism, Saitama Children’s Medical Center, Saitama, Japan

5. Department of Endocrinology and Metabolism, Kanagawa Children’s Medical Center, Kanagawa, Japan

6. Department of Obstetrics and Gynecology, Hyogo College of Medicine, Hyogo, Japan

7. Division of Pediatrics and Perinatology, Tottori University Faculty of Medicine, Tottori, Japan

8. Department of Pediatrics, Okayama University Hospital, Okayama, Japan

9. Department of Pediatrics, Sendai City Hospital, Miyagi, Japan

Publisher

Japanese Society for Pediatric Endocrinology

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health

Link

https://www.jstage.jst.go.jp/article/cpe/29/1/29_2019-0022/_pdf

Reference47 articles.

1. 1. Mornet, E. Hypophosphatasia. Best Pract Res Clin Rheumatol 2008;22: 113–27.

2. 2. Whyte, MP. Hypophosphatasia: An overview For 2017. Bone 2017;102: 15–25.

3. 3. Watanabe, A, Karasugi, T, Sawai, H, Naing, BT, Ikegawa, S, Orimo, H, et al. Prevalence of c.1559delT in ALPL, a common mutation resulting in the perinatal (lethal) form of hypophosphatasia in Japanese and effects of the mutation on heterozygous carriers. J Hum Genet 2011;56: 166–8.

4. 4. Ozono, K, Michigami, T. Hypophosphatasia now draws more attention of both clinicians and researchers: a commentary on Prevalence of c. 1559delT in ALPL, a common mutation resulting in the perinatal (lethal) form of hypophosphatasias in Japanese and effects of the mutation on heterozygous carriers. J Hum Genet 2011;56: 174–6.

5. 5. Michigami, T, Uchihashi, T, Suzuki, A, Tachikawa, K, Nakajima, S, Ozono, K. Common mutations F310L and T1559del in the tissue-nonspecific alkaline phosphatase gene are related to distinct phenotypes in Japanese patients with hypophosphatasia. Eur J Pediatr 2005;164: 277–82.

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