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Article

XLH Matters 2022: Insights and recommendations to improve outcomes for people living with X-linked hypophosphataemia (XLH)

26 Oct 2023

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 37885021
DOI: 10.1186/s13023-023-02883-3

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XLH Matters 2022: Insights and recommendations to improve outcomes for people living with X-linked hypophosphataemia (XLH)PMID 37885021Read ↗

The International X-Linked Hypophosphataemia (XLH) Registry: first interim analysis of baseline demographic, genetic and clinical dataSemantic proximity Read ↗

The International X-Linked Hypophosphatemia (XLH) Registry: first interim analysis of baseline demographic, genetic and clinical data.Semantic proximity Read ↗

The international X-linked hypophosphataemia (XLH) registry (NCT03193476): rationale for and description of an international, observational studySemantic proximity Read ↗

Expert consensus on evidence-based recommendations for the diagnosis, treatment, and follow-up of X-linked hypophosphatemic rickets (XLH)Semantic proximity Read ↗

Molecular Diagnoses of X-Linked and Other Genetic Hypophosphatemias: Results From a Sponsored Genetic Testing ProgramSemantic proximity Read ↗

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Consensus Recommendations for the Diagnosis and Management of X-Linked Hypophosphatemia in Belgium.Semantic proximity Read ↗

Patient-reported outcomes measures of X-linked hypophosphataemia participants: findings from a prospective cohort study in the UKSemantic proximity Read ↗

Novel PHEX gene locus‐specific database: Comprehensive characterization of vast number of variants associated with X‐linked hypophosphatemia (XLH)Semantic proximity Read ↗

X-linked hypophosphatemia: The medical expert's challenges and the patient's concerns on their journey with the disease.Semantic proximity Read ↗

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Spectrum of PHEX Mutations and FGF23 Profiles in a Taiwanese Cohort With X-Linked Hypophosphatemia Including 102 Patients.Semantic proximity Read ↗

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