Infantile hypophosphatasia: Treatment options to control hypercalcemia, hypercalciuria, and chronic bone demineralization

Author:

Barcia John P.,Strife C. Frederic,Langman Craig B.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference15 articles.

1. Infantile hypophosphatasia: localization within chromosome region 1p36.1-34 and prenatal diagnosis using linked DNA markers;Greenberg;Am J Hum Genet,1990

2. Hypophosphatasia and the role of alkaline phosphatase in skeletal mineralization;Whyte;Endocr Rev,1994

3. Hypophosphatasia: pediatric forms;Caswell;J Pediatr Endocrinol,1989

4. Normal values for random urinary calcium to creatinine ratios in infancy;Sargent;J Pediatr,1993

5. Hypophosphatasia: a new developmental anomaly;Rathbun;Am J Dis Child,1948

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1. Rare Causes of Hypercalcemia: 2021 Update;The Journal of Clinical Endocrinology & Metabolism;2021-07-08

2. Disorders of calcium metabolism;Handbook of Diagnostic Endocrinology;2021

3. Ionomycin ameliorates hypophosphatasia via rescuing alkaline phosphatase deficiency-mediated L-type Ca2+ channel internalization in mesenchymal stem cells;Bone Research;2020-04-26

4. Perinatal Hypophosphatasia in a Premature Infant;American Journal of Perinatology Reports;2020-04

5. Clinical Practice Guidelines for Hypophosphatasia*;Clinical Pediatric Endocrinology;2020

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