Asfotase alfa treatment in perinatal and infantile hypophosphatasia: safe and sustained efficacy
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism,Internal Medicine
Reference16 articles.
1. Enzyme-replacement therapy in life-threatening hypophosphatasia;Whyte;N Engl J Med,2012
2. Asfotase alfa treatment improves survival for perinatal and infantile hypophosphatasia;Whyte;J Clin Endocrinol Metab,2016
3. Alkaline phosphatase and hypophosphatasia;Millán;Calcif Tissue Int,2016
4. Inactivation of two mouse alkaline phosphatase genes and establishment of a model of infantile hypophosphatasia;Narisawa;Dev Dyn,1997
5. Mice lacking tissue non-specific alkaline phosphatase die from seizures due to defective metabolism of vitamin B-6;Waymire;Nat Genet,1995
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1. Effective dual-mode turn-on sensing of phosphates enabled by the twisted “head-to-head” self-assembly of a platinum(ii)-terpyridyl complex with close Pt–Pt packing;Journal of Materials Chemistry C;2024
2. The impact of enzyme replacement therapy on the oral health manifestations of hypophosphatasia among children: a scoping review;European Archives of Paediatric Dentistry;2023-04-10
3. Deletion of the Pyrophosphate Generating Enzyme ENPP1 Rescues Craniofacial Abnormalities in the TNAP−/− Mouse Model of Hypophosphatasia and Reveals FGF23 as a Marker of Phenotype Severity;Frontiers in Dental Medicine;2022-04-28
4. Pulmonary Manifestations of Endocrine and Metabolic Diseases in Children;Pediatric Clinics of North America;2021-02
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