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Page 1
Continuous subcutaneous insulin infusion versus multiple daily injection regimens in children and young people at diagnosis of type 1 diabetes: pragmatic randomised controlled trial and economic evaluation.
Blair JC, McKay A, Ridyard C, Thornborough K, Bedson E, Peak M, Didi M, Annan F, Gregory JW, Hughes DA, Gamble C; SCIPI investigators. Blair JC, et al. Among authors: didi m. BMJ. 2019 Apr 3;365:l1226. doi: 10.1136/bmj.l1226. BMJ. 2019. PMID: 30944112 Free PMC article. Clinical Trial.
Congenital hyperinsulinism due to mutations in HNF1A.
Yau D, Colclough K, Natarajan A, Parikh R, Canham N, Didi M, Senniappan S, Banerjee I. Yau D, et al. Among authors: didi m. Eur J Med Genet. 2020 Jun;63(6):103928. doi: 10.1016/j.ejmg.2020.103928. Epub 2020 Apr 20. Eur J Med Genet. 2020. PMID: 32325224
Variation in Glycemic Outcomes in Focal Forms of Congenital Hyperinsulinism-The UK Perspective.
Dastamani A, Yau D, Gilbert C, Morgan K, De Coppi P, Craigie RJ, Bomanji J, Biassoni L, Sajjan R, Flanagan SE, Houghton JAL, Senniappan S, Didi M, Dunne MJ, Banerjee I, Shah P. Dastamani A, et al. Among authors: didi m. J Endocr Soc. 2022 Mar 15;6(6):bvac033. doi: 10.1210/jendso/bvac033. eCollection 2022 Jun 1. J Endocr Soc. 2022. PMID: 35592516 Free PMC article.
Somatic mutations and progressive monosomy modify SAMD9-related phenotypes in humans.
Buonocore F, Kühnen P, Suntharalingham JP, Del Valle I, Digweed M, Stachelscheid H, Khajavi N, Didi M, Brady AF, Blankenstein O, Procter AM, Dimitri P, Wales JKH, Ghirri P, Knöbl D, Strahm B, Erlacher M, Wlodarski MW, Chen W, Kokai GK, Anderson G, Morrogh D, Moulding DA, McKee SA, Niemeyer CM, Grüters A, Achermann JC. Buonocore F, et al. Among authors: didi m. J Clin Invest. 2017 May 1;127(5):1700-1713. doi: 10.1172/JCI91913. Epub 2017 Mar 27. J Clin Invest. 2017. PMID: 28346228 Free PMC article.
47 results