Special Issue: “X-Linked Hypophosphatemia”-Reference-Cited by-同舟云学术

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Special Issue: “X-Linked Hypophosphatemia”

Published:2023-11-16 Issue:4 Volume:4 Page:720-721
ISSN:2673-396X
Container-title:Endocrines
language:en
Short-container-title:Endocrines

Author:

Fukumoto Seiji¹^ORCID,Hasegawa Yukihiro²^ORCID

Affiliation:

1. Department of Diabetes and Endocrinology, Tamaki-Aozora Hospital, Kitakashiya 56-1, Hayabuchi, Kokufucho, Tokushima 779-3125, Japan

2. Division of Endocrinology and Metabolism, Tokyo Metropolitan Children Medical Center, 2-8-29 Musashidai, Fuchu-shi, Tokyo 183-8561, Japan

Abstract

Rickets and osteomalacia are associated with impaired mineralization in growth plate cartilage and the bone osteoid [...]

Publisher

MDPI AG

Subject

General Medicine

Link

https://www.mdpi.com/2673-396X/4/4/52/pdf

Reference5 articles.

1. Studies on experimental rickets. XXI. An experimental demonstration of the existence of a vitamin which promotes calcium deposition;McCollum;J. Biol. Chem.,1922

2. Rickets resistant to vitamin D therapy;Albright;Am. J. Dis. Child.,1937

3. A genetic study of familial hypophosphatemia and vitamin D-resistant rickets with a review of the literature;Winters;Medicine,1958

4. The HYP Consortium (1995). A gene (PEX) with homologies to endopeptidases is mutated in patients with X-linked hypophosphatemic rickets. Nat. Genet., 11, 130–136.

5. ADHR Consortium (2000). Autosomal dominant hypophosphatemic rickets is associated with mutations in FGF23. Nat. Genet., 26, 345–348.

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