Biochemical algorithm to identify individuals with ALPL variants among subjects with persistent hypophosphatasaemia
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ALPL Genotypes in Patients With Atypical Femur Fractures or Other Biochemical and Clinical Signs of Hypophosphatasia
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Generalized Uncoupled Bone Remodeling Associated With Delayed Healing of Fatigue Fractures
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Radiological evaluation of pseudofracture after the administration of asfotase alfa in an adult with benign prenatal hypophosphatasia: A case report
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Genetic disorders of calcium, phosphorus, and bone homeostasis
Calcium and phosphorus [in the form of phosphate (H2PO4-/HPO4–2)] are the most abundant elements in the body where they subserve many functions – …
Winter 2021 Newsletter
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HPP and Pain Management
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Evaluation of alveolar bone hypomineralization in pediatric hypophosphatasia using orthopantomography
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