Clinical Diversity in Focal Congenital Hyperinsulinism in Infancy Correlates with Histological Heterogeneity of Islet Cell Lesions

Autor: Craigie, Ross J., Salomon-Estebanez, Maria, Yau, Daphne, Han, Bing, Mal, Walaa, Newbould, Melanie, Cheesman, Edmund, Bitetti, Stefania, Mohamed, Zainab, Sajjan, Rakesh, Padidela, Raja, Skae, Mars, Flanagan, Sarah, Ellard, Sian, Cosgrove, Karen E., Banerjee, Indraneel, Dunne, Mark J.

Publikováno v: Craigie, R, Salomon Estebanez, M, Yau, D, Han, B, Mal, W, Newbould, M, Cheesman, E, Bitetti, S, Mohamed, Z, Sajjan, R, Padidela, R, Skae, M, Flanagan, S, Ellard, S, Cosgrove, K, Banerjee, I & Dunne, M 2018, ' Clinical Diversity in Focal Congenital Hyperinsulinism in Infancy Correlates with Histological Heterogeneity of Islet Cell Lesions ', Frontiers in Endocrinology, vol. 9, no. 619 . https://doi.org/10.3389/fendo.2018.00619
Frontiers in Endocrinology

Background: Congenital Hyperinsulinism (CHI) is an important cause of severe and persistent hypoglycaemia in infancy and childhood. The focal form (CHI-F) of CHI can be potentially cured by pancreatic lesionectomy. While diagnostic characteristics of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::8985d935290802b3daadef86f497434c
https://doi.org/10.3389/fendo.2018.00619

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.