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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: salomon estebanez m. 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.
Delayed Resolution of Feeding Problems in Patients With Congenital Hyperinsulinism.
Worth C, Hall C, Wilson S, Gilligan N, O'Shea E, Salomon-Estebanez M, Dunne M, Banerjee I. Worth C, et al. Among authors: salomon estebanez m. Front Endocrinol (Lausanne). 2020 Mar 18;11:143. doi: 10.3389/fendo.2020.00143. eCollection 2020. Front Endocrinol (Lausanne). 2020. PMID: 32256453 Free PMC article.
Clinical Diversity in Focal Congenital Hyperinsulinism in Infancy Correlates With Histological Heterogeneity of Islet Cell Lesions.
Craigie RJ, Salomon-Estebanez M, Yau D, Han B, Mal W, Newbould M, Cheesman E, Bitetti S, Mohamed Z, Sajjan R, Padidela R, Skae M, Flanagan S, Ellard S, Cosgrove KE, Banerjee I, Dunne MJ. Craigie RJ, et al. Among authors: salomon estebanez m. Front Endocrinol (Lausanne). 2018 Oct 17;9:619. doi: 10.3389/fendo.2018.00619. eCollection 2018. Front Endocrinol (Lausanne). 2018. PMID: 30386300 Free PMC article.
Conservatively treated Congenital Hyperinsulinism (CHI) due to K-ATP channel gene mutations: reducing severity over time.
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 KE, Dunne MJ, Banerjee I. Salomon-Estebanez M, et al. Orphanet J Rare Dis. 2016 Dec 1;11(1):163. doi: 10.1186/s13023-016-0547-3. Orphanet J Rare Dis. 2016. PMID: 27908292 Free PMC article.
25 results