X-linked hypophosphatemia: The medical expert's challenges and the patient's concerns on their journey with the disease
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference20 articles.
1. X-linked hypophosphatemia: the mutant gene is expressed in teeth as well as in kidney;Shields;Am J Hum Genet,1990
2. Familial hypophosphatemic vitamin D-resistant rickets: dental findings and histologic study of teeth;Murayama;Oral Surg Oral Med Oral Pathol Oral Radiol Endod,2000
3. Genetic disorders of renal phosphate transport;Prie;N Engl J Med,2010
4. A clinician's guide to X-linked hypophosphatemia;Carpenter;J Bone Miner Res,2011
5. Mutational analysis of PHEX, FGF23 and CLCN5 in patients with hypophosphataemic rickets;Guven;Clin Endocrinol,2017
Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. XLH Matters 2022: Insights and recommendations to improve outcomes for people living with X-linked hypophosphataemia (XLH);Orphanet Journal of Rare Diseases;2023-10-27
2. X-Linked Familial Hypophosphatemia: A Case Report of 27-Year Old Male and Review of Literature;Hormone and Metabolic Research;2023-10
3. X-linked hypophosphatemic rickets: cases series and literature review with a focus on neurosurgical management;AboutOpen;2023-03-07
4. Effects of Burosumab Treatment on Two Siblings with X-Linked Hypophosphatemia. Case Report and Literature Review;Genes;2022-08-04
5. X-linked hypophosphatemia, a genetic and treatable cause of rickets!;Archives de Pédiatrie;2021-10
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