Conservatively treated Congenital Hyperinsulinism (CHI) due to K-ATP channel gene mutations: reducing severity over time

Salomon-Estebanez Maria (Contributor)
Sarah E. Flanagan (Contributor)
Sian Ellard (Contributor)
Lindsey Rigby (Contributor)
Louise Bowden (Contributor)
Zainab Mohamed (Contributor)
Jacqueline Nicholson (Contributor)
Mars Skae (Contributor)
Caroline Hall (Contributor)
Ross Craigie (Contributor)
Raja Padidela (Contributor)
Nuala Murphy (Contributor)
Tabitha Randell (Contributor)
Karen Cosgrove (Contributor)
Mark Dunne (Contributor)
Indraneel Banerjee (Contributor)

Dataset

1 Article

1 results

2016

Conservatively treated Congenital Hyperinsulinism (CHI) due to K-ATP channel gene mutations: reducing severity over time
Salomon Estebanez, M., Flanagan, S. E., Ellard, S., Rigby, L., Bowden, L., Mohamed, Z., Nicholson, J., Skae, M., Hall, C., Craigie, R., Padidela, R., Murphy, N., Randell, T., Cosgrove, K., Dunne, M. & Banerjee, I., 1 Dec 2016, In: Orphanet Journal of Rare Diseases. p. 163
Research output: Contribution to journal › Article › peer-review

Open Access