Urine phosphoethanolamine is a specific biomarker for hypophosphatasia in adults
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Tag: ALP
The Clinical Picture of Patients Suffering from Hypophosphatasia—A Rare Metabolic Disease of Many Faces
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Dissecting Mutational Allosteric Effects in Alkaline Phosphatases Associated with Different Hypophosphatasia Phenotypes: An Integrative Computational Investigation
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Evaluation of alveolar bone hypomineralization in pediatric hypophosphatasia using orthopantomography
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Screening for hypophosphatasia: does biochemistry lead the way?
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Genetic characterization of a large cohort of individuals with a clinical suspicion of hypophosphatasia in the United States
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Low ALP: Could it be HPP?
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SUN-LB64 Urine Phosphoethanolamine Is an Underutilized Biomarker for Hypophosphastasia
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Genotype–Phenotype Associations in 72 Adults with Suspected ALPL-Associated Hypophosphatasia
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