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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1997 2
1998 1
2001 3
2002 5
2003 6
2004 8
2005 6
2006 12
2007 12
2008 7
2009 7
2010 13
2011 8
2012 3
2013 4
2014 4
2015 1
2016 4
2022 1
2024 0

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PubMed (Bookshelf cited) for id: 371484

97 results

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Page 1
Isolated Pancreatic Aplasia Due to a Hypomorphic PTF1A Mutation.
Houghton JA, Swift GH, Shaw-Smith C, Flanagan SE, de Franco E, Caswell R, Hussain K, Mohamed S, Abdulrasoul M, Hattersley AT, MacDonald RJ, Ellard S. Houghton JA, et al. Diabetes. 2016 Sep;65(9):2810-5. doi: 10.2337/db15-1666. Epub 2016 Jun 9. Diabetes. 2016. PMID: 27284104 Free PMC article.
13. Diabetes Care in the Hospital.
American Diabetes Association. American Diabetes Association. Diabetes Care. 2016 Jan;39 Suppl 1:S99-104. doi: 10.2337/dc16-S016. Diabetes Care. 2016. PMID: 26696689 Review. No abstract available.
11. Children and Adolescents.
American Diabetes Association. American Diabetes Association. Diabetes Care. 2016 Jan;39 Suppl 1:S86-93. doi: 10.2337/dc16-S014. Diabetes Care. 2016. PMID: 26696687 Review. No abstract available.
GATA4 mutations are a cause of neonatal and childhood-onset diabetes.
Shaw-Smith C, De Franco E, Lango Allen H, Batlle M, Flanagan SE, Borowiec M, Taplin CE, van Alfen-van der Velden J, Cruz-Rojo J, Perez de Nanclares G, Miedzybrodzka Z, Deja G, Wlodarska I, Mlynarski W, Ferrer J, Hattersley AT, Ellard S. Shaw-Smith C, et al. Diabetes. 2014 Aug;63(8):2888-94. doi: 10.2337/db14-0061. Epub 2014 Apr 2. Diabetes. 2014. PMID: 24696446 Free PMC article.
Analysis of transcription factors key for mouse pancreatic development establishes NKX2-2 and MNX1 mutations as causes of neonatal diabetes in man.
Flanagan SE, De Franco E, Lango Allen H, Zerah M, Abdul-Rasoul MM, Edge JA, Stewart H, Alamiri E, Hussain K, Wallis S, de Vries L, Rubio-Cabezas O, Houghton JA, Edghill EL, Patch AM, Ellard S, Hattersley AT. Flanagan SE, et al. Cell Metab. 2014 Jan 7;19(1):146-54. doi: 10.1016/j.cmet.2013.11.021. Cell Metab. 2014. PMID: 24411943 Free PMC article.
Microcephaly, epilepsy, and neonatal diabetes due to compound heterozygous mutations in IER3IP1: insights into the natural history of a rare disorder.
Shalev SA, Tenenbaum-Rakover Y, Horovitz Y, Paz VP, Ye H, Carmody D, Highland HM, Boerwinkle E, Hanis CL, Muzny DM, Gibbs RA, Bell GI, Philipson LH, Greeley SA. Shalev SA, et al. Pediatr Diabetes. 2014 May;15(3):252-6. doi: 10.1111/pedi.12086. Epub 2013 Oct 21. Pediatr Diabetes. 2014. PMID: 24138066 Free PMC article.
97 results