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Standardised practices in the networked management of congenital hyperinsulinism: a UK national collaborative consensus.
Shaikh MG, Lucas-Herald AK, Dastamani A, Salomon Estebanez M, Senniappan S, Abid N, Ahmad S, Alexander S, Avatapalle B, Awan N, Blair H, Boyle R, Chesover A, Cochrane B, Craigie R, Cunjamalay A, Dearman S, De Coppi P, Erlandson-Parry K, Flanagan SE, Gilbert C, Gilligan N, Hall C, Houghton J, Kapoor R, McDevitt H, Mohamed Z, Morgan K, Nicholson J, Nikiforovski A, O'Shea E, Shah P, Wilson K, Worth C, Worthington S, Banerjee I. Shaikh MG, et al. Among authors: banerjee i. Front Endocrinol (Lausanne). 2023 Oct 30;14:1231043. doi: 10.3389/fendo.2023.1231043. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 38027197 Free PMC article. Review.
Continuous glucose monitoring for children with hypoglycaemia: Evidence in 2023.
Worth C, Hoskyns L, Salomon-Estebanez M, Nutter PW, Harper S, Derks TGJ, Beardsall K, Banerjee I. Worth C, et al. Among authors: banerjee i. Front Endocrinol (Lausanne). 2023 Jan 23;14:1116864. doi: 10.3389/fendo.2023.1116864. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 36755920 Free PMC article. Review.
Editorial: The problem of childhood hypoglycaemia.
Banerjee I, Mohnike K. Banerjee I, et al. Front Endocrinol (Lausanne). 2023 May 22;14:1211933. doi: 10.3389/fendo.2023.1211933. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 37284219 Free PMC article. No abstract available.
Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the loss of FOXA2 or its regulatory elements.
Laver TW, Wakeling MN, Caswell RC, Bunce B, Yau D, Männistö JME, Houghton JAL, Hopkins JJ, Weedon MN, Saraff V, Kershaw M, Honey EM, Murphy N, Giri D, Nath S, Tangari Saredo A, Banerjee I, Hussain K, Owens NDL, Flanagan SE. Laver TW, et al. Among authors: banerjee i. Eur J Hum Genet. 2024 Apr 11. doi: 10.1038/s41431-024-01593-z. Online ahead of print. Eur J Hum Genet. 2024. PMID: 38605124
642 results