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Page 1
Thyroid function test interpretation for general paediatricians.
Hardy AIA, Tetlow L, Patel L, Banerjee I. Hardy AIA, et al. Among authors: banerjee i. Arch Dis Child Educ Pract Ed. 2024 Dec 10:edpract-2024-327932. doi: 10.1136/archdischild-2024-327932. Online ahead of print. Arch Dis Child Educ Pract Ed. 2024. PMID: 39658139
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.
Editorial: The problem of childhood hypoglycemia, volume II.
Banerjee I, Mohnike K. Banerjee I, et al. Front Endocrinol (Lausanne). 2024 Apr 29;15:1412976. doi: 10.3389/fendo.2024.1412976. eCollection 2024. Front Endocrinol (Lausanne). 2024. PMID: 38742203 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 Jul;32(7):813-818. doi: 10.1038/s41431-024-01593-z. Epub 2024 Apr 11. Eur J Hum Genet. 2024. PMID: 38605124 Free PMC article.
676 results