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Health problems of adolescent and adult patients with 21-hydroxylase deficiency
Twenty-one-hydroxylase deficiency (21-OHD) is one of the most common forms of congenital adrenal hyperplasias. Since the disease requires life-long steroid hormone replacement, transition from pediatric clinical care to adolescent and adult care is necessary. Recently, several studies have shown tha...
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| Publicado no: | Clin Pediatr Endocrinol |
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| Autor principal: | |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The Japanese Society for Pediatric Endocrinology
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6207803/ https://ncbi.nlm.nih.gov/pubmed/30393437 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1297/cpe.27.203 |
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