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Genetics of neonatal hyperinsulinism

Congenital hyperinsulinism (HI) is a clinically and genetically heterogeneous entity. The clinical heterogeneity is manifested by severity ranging from extremely severe, life threatening disease to very mild clinical symptoms, which may even be difficult to identify. Furthermore, clinical responsive...

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Detalhes bibliográficos
Main Authors: Glaser, B., Thornton, P., Otonkoski, T., Junien, C.
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Group 2000
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1721059/
https://ncbi.nlm.nih.gov/pubmed/10685979
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/fn.82.2.F79
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