Extreme caution on the use of sirolimus for the congenital hyperinsulinism in infancy patient

Por Banerjee, Indraneel, De Leon, Diva, Dunne, Mark J.
Publicado no Orphanet J Rare Dis (2017)

Can network biology unravel the aetiology of congenital hyperinsulinism?

Por Stevens, Adam, Cosgrove, Karen E, Padidela, Raja, Skae, Mars S, Clayton, Peter E, Banerjee, Indraneel, Dunne, Mark J
Publicado em 2013

PAX4 Enhances Beta-Cell Differentiation of Human Embryonic Stem Cells

Por Liew, Chee Gee, Shah, Nadia N., Briston, Sarah J., Shepherd, Ruth M., Khoo, Cheen Peen, Dunne, Mark J., Moore, Harry D., Cosgrove, Karen E., Andrews, Peter W.
Publicado em 2008

In Vitro Recovery of ATP-Sensitive Potassium Channels in β-Cells From Patients With Congenital Hyperinsulinism of Infancy

Por Powell, Philippa D., Bellanné-Chantelot, Christine, Flanagan, Sarah E., Ellard, Sian, Rooman, Raoul, Hussain, Khalid, Skae, Mars, Clayton, Peter, de Lonlay, Pascale, Dunne, Mark J., Cosgrove, Karen E.
Publicado em 2011

Feeding Problems Are Persistent in Children with Severe Congenital Hyperinsulinism

Por Banerjee, Indraneel, Forsythe, Lynette, Skae, Mars, Avatapalle, Hima Bindu, Rigby, Lindsey, Bowden, Louise E., Craigie, Ross, Padidela, Raja, Ehtisham, Sarah, Patel, Leena, Cosgrove, Karen E., Dunne, Mark J., Clayton, Peter E.
Publicado no Front Endocrinol (Lausanne) (2016)

Reduced Glycemic Variability in Diazoxide-Responsive Children with Congenital Hyperinsulinism Using Supplemental Omega-3-Polyunsaturated Fatty Acids; A Pilot Trial with MaxEPA(R)

Por Skae, Mars, Avatapalle, Hima Bindu, Banerjee, Indraneel, Rigby, Lindsey, Vail, Andy, Foster, Peter, Charalambous, Christiana, Bowden, Louise, Padidela, Raja, Patel, Leena, Ehtisham, Sarah, Cosgrove, Karen E., Dunne, Mark J., Clayton, Peter E.
Publicado em 2014

Abnormal Neurodevelopmental Outcomes are Common in Children with Transient Congenital Hyperinsulinism

Por Avatapalle, Hima Bindu, Banerjee, Indraneel, Shah, Sajni, Pryce, Megan, Nicholson, Jacqueline, Rigby, Lindsey, Caine, Louise, Didi, Mohammed, Skae, Mars, Ehtisham, Sarah, Patel, Leena, Padidela, Raja, Cosgrove, Karen E., Dunne, Mark J., Clayton, Peter E.
Publicado em 2013

Enhanced Islet Cell Nucleomegaly Defines Diffuse Congenital Hyperinsulinism in Infancy but Not Other Forms of the Disease

Por Han, Bing, Newbould, Melanie, Batra, Gauri, Cheesman, Edmund, Craigie, Ross J., Mohamed, Zainab, Rigby, Lindsey, Padidela, Raja, Skae, Mars, Mironov, Aleksandr, Starborg, Tobias, Kadler, Karl E., Cosgrove, Karen E., Banerjee, Indraneel, Dunne, Mark J.
Publicado no Am J Clin Pathol (2016)

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

Por Salomon-Estebanez, Maria, Flanagan, Sarah E., Ellard, Sian, Rigby, Lindsey, Bowden, Louise, Mohamed, Zainab, Nicholson, Jacqueline, Skae, Mars, Hall, Caroline, Craigie, Ross, Padidela, Raja, Murphy, Nuala, Randell, Tabitha, Cosgrove, Karen E., Dunne, Mark J., Banerjee, Indraneel
Publicado no Orphanet J Rare Dis (2016)

Altered Phenotype of β-Cells and Other Pancreatic Cell Lineages in Patients With Diffuse Congenital Hyperinsulinism in Infancy Caused by Mutations in the ATP-Sensitive K-Channel

Por Salisbury, Rachel J., Han, Bing, Jennings, Rachel E., Berry, Andrew A., Stevens, Adam, Mohamed, Zainab, Sugden, Sarah A., De Krijger, Ronald, Cross, Sarah E., Johnson, Paul P.V., Newbould, Melanie, Cosgrove, Karen E., Hanley, Karen Piper, Banerjee, Indraneel, Dunne, Mark J., Hanley, Neil A.
Publicado no Diabetes (2015)