Growth in height and body proportion from birth to adulthood in hereditary hypophosphatemic rickets: a retrospective cohort study
Author:
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Link
https://link.springer.com/content/pdf/10.1007/s40618-022-01768-9.pdf
Reference40 articles.
1. Capelli S, Donghi V, Maruca K, Vezzoli G, Corbetta S, Brandi ML, Mora S, Weber G (2015) Clinical and molecular heterogeneity in a large series of patients with hypophosphatemic rickets. Bone 79(143–149):12. https://doi.org/10.1016/j.bone.2015.05.040
2. Razali NN, Hwu TT, Thilakavathy K (2015) Phosphate homeostasis and genetic mutations of familial hypophosphatemic rickets. J Pediatr Endocrinol Metab JPEM 28(9–10):1009–1017. https://doi.org/10.1515/jpem-2014-0366
3. Bastepe M, Jüppner H (2008) Inherited hypophosphatemic disorders in children and the evolving mechanisms of phosphate regulation. Rev Endocr Metab Disord 9(2):171–180. https://doi.org/10.1007/s11154-008-9075-3
4. Glorieux FH, Pettifor JM, Jüppner H (2012) Pediatric Bone. Biology and diseases. Academic Press, USA
5. Carpenter TO, Imel EA, Holm IA, Jan de Beur SM, Insogna KL (2011) A clinician’s guide to X-linked hypophosphatemia. J Bone Min Res Off J Am Soc Bone Min Res 26(7):1381–1388. https://doi.org/10.1002/jbmr.340
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