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Congenital hyperinsulinism: current trends in diagnosis and therapy
Congenital hyperinsulinism (HI) is an inappropriate insulin secretion by the pancreatic β-cells secondary to various genetic disorders. The incidence is estimated at 1/50, 000 live births, but it may be as high as 1/2, 500 in countries with substantial consanguinity. Recurrent episodes of hyperinsul...
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| Autors principals: | , , , , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2011
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3199232/ https://ncbi.nlm.nih.gov/pubmed/21967988 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1172-6-63 |
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