X-linked hypophosphatemia and burosumab: Practical clinical points from the French experience-Reference-Cited by-同舟云学术

X-linked hypophosphatemia and burosumab: Practical clinical points from the French experience

Published:2021-10 Issue:5 Volume:88 Page:105208
ISSN:1297-319X
Container-title:Joint Bone Spine
language:en
Short-container-title:Joint Bone Spine

Author:

Bacchetta Justine,Rothenbuhler Anya,Gueorguieva Iva^ORCID,Kamenicky Peter,Salles Jean-Pierre^ORCID,Briot Karine,Linglart Agnès

Publisher

Elsevier BV

Subject

Rheumatology

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3. Nationwide survey of fibroblast growth factor 23 (FGF23)-related hypophosphatemic diseases in Japan: prevalence, biochemical data, and treatment;Endo;Endocr J,2015

4. Orphanet. [Available from: https://www.orpha.net/consor/cgi-bin/Disease_Search.php?lng=FR&data_id=11911&Disease_Disease_Search_diseaseType=ORPHA&Disease_Disease_Search_diseaseGroup=89936&Disease(s)/group%20of%20diseases=XLH&title=XLH&search=Disease_Search_Simple].

5. Osteocyte regulation of phosphate homeostasis and bone mineralization underlies the pathophysiology of the heritable disorders of rickets and osteomalacia;Feng;Bone,2013

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1. Diagnosis, treatment, and management of rickets: a position statement from the Bone and Mineral Metabolism Group of the Italian Society of Pediatric Endocrinology and Diabetology;Frontiers in Endocrinology;2024-04-19

2. X-linked hypophosphatemia: The value of feedback focus groups to assess patient and caregiver needs;European Journal of Medical Genetics;2024-04

3. Raquitismos;EMC - Pediatría;2023-09

4. Transition of patients with metabolic bone disease from paediatric to adult healthcare services: current situation and proposals for improvement;Orphanet Journal of Rare Diseases;2023-08-29

5. Expert consensus on evidence-based recommendations for the diagnosis, treatment, and follow-up of X-linked hypophosphatemic rickets (XLH);2023-05-08