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Neonatal screening for congenital hypothyroidism in an Italian Centre: a 5-years real-life retrospective study
INTRODUCTION: Congenital hypothyroidism is an endocrine disease with a significant incidence in the general population (1:2000–1:3000 newborns in Italy) and a different geographical distribution, partially explained by endemic iodine deficiency, genetic traits and autoimmune thyroid diseases. OBJECT...
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| Publicat a: | Ital J Pediatr |
|---|---|
| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2021
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8097769/ https://ncbi.nlm.nih.gov/pubmed/33952334 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13052-021-01053-0 |
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