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

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

doi:10.1186/s13023-016-0547-3

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

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

Research output: Contribution to journal › Article › peer-review

Original language	English
Pages (from-to)	163
Journal	Orphanet Journal of Rare Diseases
DOIs	https://doi.org/10.1186/s13023-016-0547-3
Publication status	Published - 1 Dec 2016

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10.1186/s13023-016-0547-3Licence: CC BY

Conservatively treated Congenital Hyperinsulinism (CHI) due to K-ATP channel gene mutations: reducing severity over time
Maria, S. (Contributor), Flanagan, S. E. (Contributor), Ellard, S. (Contributor), Rigby, L. (Contributor), Bowden, L. (Contributor), Mohamed, Z. (Contributor), Nicholson, J. (Contributor), Skae, M. (Contributor), Hall, C. (Contributor), Craigie, R. (Contributor), Padidela, R. (Contributor), Murphy, N. (Contributor), Randell, T. (Contributor), Cosgrove, K. (Contributor), Dunne, M. (Contributor) & Banerjee, I. (Contributor), figshare , 1 Dec 2016
DOI: 10.6084/m9.figshare.c.3616340.v1, https://figshare.com/collections/Conservatively_treated_Congenital_Hyperinsulinism_CHI_due_to_K-ATP_channel_gene_mutations_reducing_severity_over_time/3616340/1
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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. (2016). Conservatively treated Congenital Hyperinsulinism (CHI) due to K-ATP channel gene mutations: reducing severity over time. Orphanet Journal of Rare Diseases, 163. https://doi.org/10.1186/s13023-016-0547-3

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

author = "{Salomon Estebanez}, Maria and Flanagan, {Sarah E.} and Sian Ellard and Lindsey Rigby and Louise Bowden and Zainab Mohamed and Jacqueline Nicholson and Mars Skae and Caroline Hall and Ross Craigie and Raja Padidela and Nuala Murphy and Tabitha Randell and Karen Cosgrove and Mark Dunne and Indraneel Banerjee",

year = "2016",

month = dec,

day = "1",

doi = "10.1186/s13023-016-0547-3",

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Salomon Estebanez, M, Flanagan, SE, 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 2016, 'Conservatively treated Congenital Hyperinsulinism (CHI) due to K-ATP channel gene mutations: reducing severity over time', Orphanet Journal of Rare Diseases, pp. 163. https://doi.org/10.1186/s13023-016-0547-3

TY - JOUR

T1 - Conservatively treated Congenital Hyperinsulinism (CHI) due to K-ATP channel gene mutations: reducing severity over time

AU - Salomon Estebanez, Maria

AU - Flanagan, Sarah E.

AU - Ellard, Sian

AU - Rigby, Lindsey

AU - Bowden, Louise

AU - Mohamed, Zainab

AU - Nicholson, Jacqueline

AU - Skae, Mars

AU - Hall, Caroline

AU - Craigie, Ross

AU - Padidela, Raja

AU - Murphy, Nuala

AU - Randell, Tabitha

AU - Cosgrove, Karen

AU - Dunne, Mark

AU - Banerjee, Indraneel

PY - 2016/12/1

Y1 - 2016/12/1

U2 - 10.1186/s13023-016-0547-3

DO - 10.1186/s13023-016-0547-3

M3 - Article

SN - 1750-1172

SP - 163

JO - Orphanet Journal of Rare Diseases

JF - Orphanet Journal of Rare Diseases

ER -

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

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

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