Investigation of ALPL variant states and clinical outcomes: An analysis of adults and adolescents with hypophosphatasia treated with asfotase alfa
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Tag: ALPL
TNAP as a New Player in Chronic Inflammatory Conditions and Metabolism
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Alpl prevents bone ageing sensitivity by specifically regulating senescence and differentiation in mesenchymal stem cells
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SUN-LB64 Urine Phosphoethanolamine Is an Underutilized Biomarker for Hypophosphastasia
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HPP Genetics Boot Camp – Learning More About ALPL Gene Changes and HPP in Families
Presented by The Soft Bones Foundation. Do you have questions about your family’s diagnosis of Hypophosphatasia? Are you uncertain what the risk is for other…
Can we identify individuals with an ALPL variant in adults with persistent hypophosphatasaemia?
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Incidence of Mutations in the ALPL, GGPS1, and CYP1A1 Genes in Patients With Atypical Femoral Fractures
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Outcome of teriparatide treatment on fracture healing complications and symptomatic bone marrow edema in four adult patients with hypophosphatasia
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Bisphosphonate Use and Fractures in Adults with Hypophosphatasia
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