Hypophosphatasia: Natural history study of 101 affected children investigated at one research center
Author:
Publisher
Elsevier BV
Subject
Histology,Physiology,Endocrinology, Diabetes and Metabolism
Reference19 articles.
1. Hypophosphatasia: aetiology, nosology, pathogenesis, diagnosis and treatment;Whyte;Nat. Rev. Endocrinol.,2016
2. Alkaline phosphatase and hypophosphatasia;Millan;Calcif. Tissue Int.,2016
3. Hypophosphatasia;Whyte,2013
4. Calcific periarthritis as the only clinical manifestation of hypophosphatasia in middle-aged sisters;Guanabens;J. Bone Miner. Res.,2014
5. Hypophosphatasia: validation and expansion of the clinical nosology for children from 25years experience with 173 pediatric patients;Whyte;Bone,2015
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1. Pyridoxine challenge reflects pediatric hypophosphatasia severity and thereby examines tissue-nonspecific alkaline phosphatase's role in vitamin B6 metabolism;Bone;2024-02
2. The Global ALPL gene variant classification project: Dedicated to deciphering variants;Bone;2024-01
3. The diagnosis of hypophosphatasia in children as a multidisciplinary effort: an expert opinion;Journal of Endocrinological Investigation;2023-09-26
4. Growth and disease burden in children with hypophosphatasia;Endocrine Connections;2023-03-14
5. Dental manifestation and management of hypophosphatasia;Japanese Dental Science Review;2022-11
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