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Wolfram syndrome.
Minton JA, Rainbow LA, Ricketts C, Barrett TG. Minton JA, et al. Rev Endocr Metab Disord. 2003 Mar;4(1):53-9. doi: 10.1023/a:1021875403463. Rev Endocr Metab Disord. 2003. PMID: 12618560 Review. No abstract available.
Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood.
Edghill EL, Flanagan SE, Patch AM, Boustred C, Parrish A, Shields B, Shepherd MH, Hussain K, Kapoor RR, Malecki M, MacDonald MJ, Støy J, Steiner DF, Philipson LH, Bell GI; Neonatal Diabetes International Collaborative Group; Hattersley AT, Ellard S. Edghill EL, et al. Diabetes. 2008 Apr;57(4):1034-42. doi: 10.2337/db07-1405. Epub 2007 Dec 27. Diabetes. 2008. PMID: 18162506 Free PMC article.
Syndromic obesity and diabetes: changes in body composition with age and mutation analysis of ALMS1 in 12 United Kingdom kindreds with Alstrom syndrome.
Minton JA, Owen KR, Ricketts CJ, Crabtree N, Shaikh G, Ehtisham S, Porter JR, Carey C, Hodge D, Paisey R, Walker M, Barrett TG. Minton JA, et al. Among authors: barrett tg. J Clin Endocrinol Metab. 2006 Aug;91(8):3110-6. doi: 10.1210/jc.2005-2633. Epub 2006 May 23. J Clin Endocrinol Metab. 2006. PMID: 16720663
Asian MODY: are we missing an important diagnosis?
Porter JR, Rangasami JJ, Ellard S, Gloyn AL, Shields BM, Edwards J, Anderson JM, Shaw NJ, Hattersley AT, Frayling TM, Plunkett M, Barrett TG. Porter JR, et al. Among authors: barrett tg. Diabet Med. 2006 Nov;23(11):1257-60. doi: 10.1111/j.1464-5491.2006.01958.x. Diabet Med. 2006. PMID: 17054605
Permanent neonatal diabetes in an Asian infant.
Porter JR, Shaw NJ, Barrett TG, Hattersley AT, Ellard S, Gloyn AL. Porter JR, et al. Among authors: barrett tg. J Pediatr. 2005 Jan;146(1):131-3. doi: 10.1016/j.jpeds.2004.09.008. J Pediatr. 2005. PMID: 15644838 Review.
1,708 results