High bone mineral apparent density in children with X-linked hypophosphatemia
Author:
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology, Diabetes and Metabolism
Link
http://link.springer.com/content/pdf/10.1007/s00198-013-2286-9.pdf
Reference44 articles.
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2. Beck-Nielsen SS, Brixen K, Gram J, Brusgaard K (2012) Mutational analysis of PHEX, FGF23, DMP1, SLC34A3 and CLCN5 in patients with hypophosphatemic rickets. J Hum Genet 57:453–458
3. Carpenter TO (2012) The expanding family of hypophosphatemic syndromes. J Bone Miner Metab 30:1–9
4. Rauch F (2003) The rachitic bone. Endocr Dev 6:69–79
5. Seeman E (1998) Growth in bone mass and size—are racial and gender differences in bone mineral density more apparent than real? J Clin Endocrinol Metab 83:1414–1419
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3. Evaluation of the trabecular bone score in 35 children and adults with X-linked hypophosphatemic rickets;Journal of Bone and Mineral Metabolism;2023-07-07
4. Expert consensus on evidence-based recommendations for the diagnosis, treatment, and follow-up of X-linked hypophosphatemic rickets (XLH);2023-05-08
5. Asia‐Pacific Consensus Recommendations on X‐Linked Hypophosphatemia: Diagnosis, Multidisciplinary Management, and Transition From Pediatric to Adult Care;JBMR Plus;2023-05
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