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Asfotase alfa has a limited effect in improving the bowed limbs in perinatal benign hypophosphatasia: A case report
Hypophosphatasia (HPP) is a rare skeletal dysplasia characterized by impaired bone mineralization, caused by loss-of-function mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) gene. Enzyme replacement therapy (ERT) by administration of asfotase alfa was reported to improve the surviv...
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| Publicado no: | Clin Pediatr Endocrinol |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The Japanese Society for Pediatric Endocrinology
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7783131/ https://ncbi.nlm.nih.gov/pubmed/33446953 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1297/cpe.30.53 |
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