The international X-linked hypophosphataemia (XLH) registry (NCT03193476): rationale for and description of an international, observational study
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Title
The international X-linked hypophosphataemia (XLH) registry (NCT03193476): rationale for and description of an international, observational study
Authors
Keywords
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Journal
Orphanet Journal of Rare Diseases
Volume 15, Issue 1, Pages -
Publisher
Springer Science and Business Media LLC
Online
2020-07-01
DOI
10.1186/s13023-020-01434-4
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Related references
Note: Only part of the references are listed.- FGF23 and its role in X-linked hypophosphatemia-related morbidity
- (2019) Signe Sparre Beck-Nielsen et al. Orphanet Journal of Rare Diseases
- Burosumab versus conventional therapy in children with X-linked hypophosphataemia: a randomised, active-controlled, open-label, phase 3 trial
- (2019) Erik A Imel et al. LANCET
- Clinical practice recommendations for the diagnosis and management of X-linked hypophosphataemia
- (2019) Dieter Haffner et al. Nature Reviews Nephrology
- Patient Registries: An Underused Resource for Medicines Evaluation
- (2019) Patricia McGettigan et al. DRUG SAFETY
- Comment on: “Patient Registries: An Underused Resource for Medicines Evaluation: Operational Proposals for Increasing the Use of Patient Registries in Regulatory Assessments”
- (2019) Ravi Jandhyala DRUG SAFETY
- A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Trial Evaluating the Efficacy of Burosumab, an Anti-FGF23 Antibody, in Adults With X-Linked Hypophosphatemia: Week 24 Primary Analysis
- (2018) Karl L Insogna et al. JOURNAL OF BONE AND MINERAL RESEARCH
- Excessive Osteocytic Fgf23 Secretion Contributes to Pyrophosphate Accumulation and Mineralization Defect in Hyp Mice
- (2016) Sathish K. Murali et al. PLOS BIOLOGY
- The FAIR Guiding Principles for scientific data management and stewardship
- (2016) Mark D. Wilkinson et al. Scientific Data
- Nationwide survey of fibroblast growth factor 23 (FGF23)-related hypophosphatemic diseases in Japan: prevalence, biochemical data and treatment
- (2015) Itsuro Endo et al. ENDOCRINE JOURNAL
- Hereditary hypophosphatemia in Norway: a retrospective population-based study of genotypes, phenotypes, and treatment complications
- (2015) Silje Rafaelsen et al. EUROPEAN JOURNAL OF ENDOCRINOLOGY
- The European Cystic Fibrosis Society Patient Registry: valuable lessons learned on how to sustain a disease registry
- (2014) Laura Viviani et al. Orphanet Journal of Rare Diseases
- A clinician's guide to X-linked hypophosphatemia
- (2011) Thomas O Carpenter et al. JOURNAL OF BONE AND MINERAL RESEARCH
- Pompe disease: Design, methodology, and early findings from the Pompe Registry
- (2011) Barry J. Byrne et al. MOLECULAR GENETICS AND METABOLISM
- Calcimimetics as an Adjuvant Treatment for Familial Hypophosphatemic Rickets
- (2008) U. S. Alon et al. Clinical Journal of the American Society of Nephrology
- Incidence and prevalence of nutritional and hereditary rickets in southern Denmark
- (2008) Signe Sparre Beck-Nielsen et al. EUROPEAN JOURNAL OF ENDOCRINOLOGY
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