Biochemical, clinical and genetic characteristics in adults with persistent hypophosphatasaemia; Data from an endocrinological outpatient clinic in Denmark
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Bone turnover and mineral metabolism in adult patients with hypophosphatasia treated with asfotase alfa
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Photographs reveal people behind rare illnesses
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Prenatal enzyme replacement therapy for Akp2−/− mice with lethal hypophosphatasia
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Dental effects of enzyme replacement therapy in case of childhood-type hypophosphatasia
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Compound Heterozygous PIGT Mutations in Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome: First Case in Korea and Characterization by Persistent Hypophosphatasia
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Six ALPL gene variants in five children with hypophosphatasia
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Dental outcomes for children receiving Strensiq® for Hypophosphatasia
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Tissue-Nonspecific Alkaline Phosphatase in Central Nervous System Health and Disease: A Focus on Brain Microvascular Endothelial Cells
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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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