Somatostatin receptors in congenital hyperinsulinism: Biology to bedside

Autor: Mirjam E. van Albada, Klaus Mohnike, Mark J. Dunne, Indi Banerjee, Stephen F. Betz

Publikováno v: Frontiers in Endocrinology, Vol 13 (2022)

Congenital hyperinsulinism (CHI), although a rare disease, is an important cause of severe hypoglycemia in early infancy and childhood, causing preventable morbidity and mortality. Prompt diagnosis and appropriate treatment is necessary to prevent hy

Externí odkaz: https://doaj.org/article/0e5eca2594bd4225893fb93a46fa8bb5

Evaluation of a low postnatal hypoglycaemia threshold

Autor: Chris Worth, Gokul Pon Ramya, Hashim R, Porte H, Sarah Worthington, Mark Dunne, Maria Salomon Estebanez, Mahaveer A, Indi Banerjee

Publikováno v: Endocrine Abstracts.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9b8f8835ec7c093c5104698e2dafedf2
https://doi.org/10.1530/endoabs.85.oc5.9

Therapies and outcomes of congenital hyperinsulinism-induced hypoglycaemia

Autor: Karen E. Cosgrove, Pratik Shah, Indi Banerjee, Mark J. Dunne, Jacqueline Nicholson, Maria Salomon-Estebanez

Publikováno v: Banerjee, I, Salomon Estebanez, M, Shah, P, Nicholson, J, Cosgrove, K & Dunne, M 2019, ' Therapies and outcomes of congenital hyperinsulinism-induced hypoglycaemia ', Diabetic Medicine, vol. 36, no. 1, pp. 9-21 . https://doi.org/10.1111/dme.13823
Diabetic Medicine
Banerjee, I, Salomon-estebanez, M, Shah, P, Nicholson, J, Cosgrove, K E & Dunne, M J 2018, ' Therapies and outcomes of congenital hyperinsulinism-induced hypoglycaemia ' Diabetic Medicine . DOI: 10.1111/dme.13823

Congenital hyperinsulinism is a rare disease, but is the most frequent cause of persistent and severe hypoglycaemia in early childhood. Hypoglycaemia caused by excessive and dysregulated insulin secretion (hyperinsulinism) from disordered pancreatic

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6af5ee69324837029905dfd08999fc8
https://www.research.manchester.ac.uk/portal/en/publications/therapies-and-outcomes-of-congenital-hyperinsulinisminduced-hypoglycaemia(4d865639-136f-4231-8a12-2ef1b5bb2108).html

Optimising diagnostic performance of IGF-I and IGFBP-3 measurement: importance of reference range and cut-off value

Autor: Laila Al-Hashmi, Claire Manfredonia, Peter Clayton, Lesley Tetlow, Indi Banerjee, Philip Murray

Publikováno v: Endocrine Abstracts.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d051d0916964c59e860d88aaab9068e4
https://doi.org/10.1530/endoabs.58.p023

SGPL1 Missense Mutation in an Infant with Primary Adrenal Insufficiency (PAI), Congenital Nephrotic Syndrome, Primary Hypothyroidism and Gonadal Failure

Autor: Avinaash Maharaj, Wallace, Dean, Indi Banerjee, Rathi Prasad, Metherell, Louise A

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b523da6c214cd9c3060bc36ae91911ac