Association of Serum Alkaline Phosphatase with the TG/HDL Ratio and TyG Index in Korean Adults
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Category: Scientific Publications
Neonatal seizures as onset of Inborn Errors of Metabolism (IEMs): from diagnosis to treatment. A systematic review
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Cross-sectional analysis: clinical presentation of children with persistently low ALP levels
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What Is Hypophosphatasia? An Overview of This Rare Genetic Disorder
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The Occurrence and Burden of Hypophosphatasia in an Ambulatory Care Endocrinology Practice
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Hypophosphatasia: A Unique Disorder of Bone Mineralization
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Polymorphic variants of alkaline phosphatase gene correlate with clinical signs of adult hypophosphatasia?
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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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Prenatal enzyme replacement therapy for Akp2−/− mice with lethal hypophosphatasia
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