The impact of monoallelic inactivation mutations in the ENPP1 gene on pediatric skeletal development: a case report and literature review. [PDF]
Lu S, Sun N, Li Y, Wu Z, Zhang J.
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Burosumab treatment of a child with McCune-Albright syndrome/polyostotic fibrous dysplasia: challenges and benefits. [PDF]
Sakka SD+6 more
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Diagnostic approach to rickets: an Endocrine Society of Bengal (ESB) consensus statement. [PDF]
Roy A+28 more
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Unusual PHEX variants implicate uncommon genetic mechanisms for X-linked hypophosphatemic rickets. [PDF]
Alzoebie L+4 more
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Editorial: What's new in endocrinology? volume II. [PDF]
Holly JMP+3 more
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Clinical, Radiographic, and Molecular Analysis of Patients with X-Linked Hypophosphatemic Rickets: Looking for Phenotype-Genotype Correlation. [PDF]
Olivas-Valdez MA+8 more
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Erratum: X-linked hypophosphatemic rickets and nephrocalcinosis: clinical characteriscs of a single-center pediatric cohort in North America before and after burosumab. [PDF]
Frontiers Production Office.
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