Dental effects of enzyme replacement therapy in case of childhood-type hypophosphatasia
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Category: Scientific Publications
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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Hypophosphatasia as a rare cause of neonatal seizures
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Successful treatment with bone maturation and average life expectancy of hypophosphatasia model mice by adeno-associated virus type 8-mediated neonatal gene therapy via single muscle injection
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Patient-Reported Symptomatology in Hypophosphatasia
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Polymorphic variants of alkaline phosphatase gene correlate with clinical signs of adult hypophosphatasia?
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