X-Linked Hypophosphatemia Latest Advances

Find the Latest Research About X-Linked Hypophosphatemia

Last Updated: 09/26/2026

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Found 3111 publications

Calcium Crystal Deposits in Kidney Allografts: The Interplay of PTH Levels and Phosphaturia.

Calcium Crystal Deposits in Kidney Allografts: The Interplay of PTH Levels and Phosphaturia.

Journal: Kidney medicine
Published: August 30, 2026

Correction to: Health-related quality of life in French adults with X-linked hypophosphatemia: real-world data from the International XLH Registry.

Correction to: Health-related quality of life in French adults with X-linked hypophosphatemia: real-world data from the International XLH Registry.

Journal: JBMR plus
Published: August 21, 2026

Correction to: Health-related quality of life in French pediatric patients with X-linked hypophosphatemia: real-world data from the International XLH Registry.

Correction to: Health-related quality of life in French pediatric patients with X-linked hypophosphatemia: real-world data from the International XLH Registry.

Journal: JBMR plus
Published: August 18, 2026

Etiological Spectrum, Clinical Characteristics, and Six-Month Treatment Outcomes of Refractory Rickets in Children: A Prospective Observational Cohort Study From Eastern India.

Etiological Spectrum, Clinical Characteristics, and Six-Month Treatment Outcomes of Refractory Rickets in Children: A Prospective Observational Cohort Study From Eastern India.

Journal: Cureus
Published: August 07, 2026

Sinonasal Phosphaturic Mesenchymal Tumor Presenting With Tumor-Induced Osteomalacia: A Rare Case and Review of the Literature.

Sinonasal Phosphaturic Mesenchymal Tumor Presenting With Tumor-Induced Osteomalacia: A Rare Case and Review of the Literature.

Journal: Cureus
Published: August 02, 2026

Autosomal recessive hypophosphatemic rickets/osteomalacia caused by a novel mutation in the DMP1 gene: a case report and literature review

Autosomal recessive hypophosphatemic rickets/osteomalacia caused by a novel mutation in the DMP1 gene: a case report and literature review

Journal: Zhonghua nei ke za zhi
Published: July 10, 2026

A Diagnostic Dilemma: Hypophosphatemic Rickets Unmasking Tyrosinemia Type 1: A Case Report.

A Diagnostic Dilemma: Hypophosphatemic Rickets Unmasking Tyrosinemia Type 1: A Case Report.

Journal: Clinical case reports
Published: July 01, 2026

Correction: Transition Care for Young People with Rare Bone and Mineral Conditions: A Scoping Review.

Correction: Transition Care for Young People with Rare Bone and Mineral Conditions: A Scoping Review.

Journal: Advances in therapy
Published: June 18, 2026

Fibroblast Growth Factor 23 (FGF23): From Synthesis to Cleavage.

Fibroblast Growth Factor 23 (FGF23): From Synthesis to Cleavage.

Journal: Molecular and cellular endocrinology
Published: June 11, 2026

X-linked Hypophosphatemic Rickets Revealed by Exome Sequencing: A Pediatric Case Report of a PHEX Pathogenic Variant.

X-linked Hypophosphatemic Rickets Revealed by Exome Sequencing: A Pediatric Case Report of a PHEX Pathogenic Variant.

Journal: Cureus
Published: May 25, 2026

Adverse health outcomes across the life course in individuals with six rare bone diseases: a 10-year population-based cohort study.

Adverse health outcomes across the life course in individuals with six rare bone diseases: a 10-year population-based cohort study.

Journal: European journal of endocrinology
Published: May 23, 2026

Hypophosphatemic rickets: diagnosis and treatment.

Hypophosphatemic rickets: diagnosis and treatment.

Journal: Archives of endocrinology and metabolism
Published: May 15, 2026
Showing 1-12 of 3,111

Last Updated: 09/26/2026