Stride A - Search Results

1

Microalbuminuria as a screening tool in cystic fibrosis-related diabetes.

Dobson L, Stride A, Bingham C, Elworthy S, Sheldon CD, Hattersley AT. Dobson L, et al. Among authors: stride a. Pediatr Pulmonol. 2005 Feb;39(2):103-7. doi: 10.1002/ppul.20124. Pediatr Pulmonol. 2005. PMID: 15573388

2

Different genes, different diabetes: lessons from maturity-onset diabetes of the young.

Stride A, Hattersley AT. Stride A, et al. Ann Med. 2002;34(3):207-16. Ann Med. 2002. PMID: 12173691 Review.

3

Beta-cell dysfunction, insulin sensitivity, and glycosuria precede diabetes in hepatocyte nuclear factor-1alpha mutation carriers.

Stride A, Ellard S, Clark P, Shakespeare L, Salzmann M, Shepherd M, Hattersley AT. Stride A, et al. Diabetes Care. 2005 Jul;28(7):1751-6. doi: 10.2337/diacare.28.7.1751. Diabetes Care. 2005. PMID: 15983330

4

Etiological investigation of diabetes in young adults presenting with apparent type 2 diabetes.

Owen KR, Stride A, Ellard S, Hattersley AT. Owen KR, et al. Among authors: stride a. Diabetes Care. 2003 Jul;26(7):2088-93. doi: 10.2337/diacare.26.7.2088. Diabetes Care. 2003. PMID: 12832318

5

Intrauterine hyperglycemia is associated with an earlier diagnosis of diabetes in HNF-1alpha gene mutation carriers.

Stride A, Shepherd M, Frayling TM, Bulman MP, Ellard S, Hattersley AT. Stride A, et al. Diabetes Care. 2002 Dec;25(12):2287-91. doi: 10.2337/diacare.25.12.2287. Diabetes Care. 2002. PMID: 12453975

6

Isomers of the TCF1 gene encoding hepatocyte nuclear factor-1 alpha show differential expression in the pancreas and define the relationship between mutation position and clinical phenotype in monogenic diabetes.

Harries LW, Ellard S, Stride A, Morgan NG, Hattersley AT. Harries LW, et al. Among authors: stride a. Hum Mol Genet. 2006 Jul 15;15(14):2216-24. doi: 10.1093/hmg/ddl147. Epub 2006 Jun 7. Hum Mol Genet. 2006. PMID: 16760222

7

Insights into the structure and regulation of glucokinase from a novel mutation (V62M), which causes maturity-onset diabetes of the young.

Gloyn AL, Odili S, Zelent D, Buettger C, Castleden HA, Steele AM, Stride A, Shiota C, Magnuson MA, Lorini R, d'Annunzio G, Stanley CA, Kwagh J, van Schaftingen E, Veiga-da-Cunha M, Barbetti F, Dunten P, Han Y, Grimsby J, Taub R, Ellard S, Hattersley AT, Matschinsky FM. Gloyn AL, et al. Among authors: stride a. J Biol Chem. 2005 Apr 8;280(14):14105-13. doi: 10.1074/jbc.M413146200. Epub 2005 Jan 25. J Biol Chem. 2005. PMID: 15677479 Free article.

8

Cross-sectional and longitudinal studies suggest pharmacological treatment used in patients with glucokinase mutations does not alter glycaemia.

Stride A, Shields B, Gill-Carey O, Chakera AJ, Colclough K, Ellard S, Hattersley AT. Stride A, et al. Diabetologia. 2014 Jan;57(1):54-6. doi: 10.1007/s00125-013-3075-x. Epub 2013 Oct 4. Diabetologia. 2014. PMID: 24092492 Free PMC article.

9

beta-cell genes and diabetes: quantitative and qualitative differences in the pathophysiology of hepatic nuclear factor-1alpha and glucokinase mutations.

Pearson ER, Velho G, Clark P, Stride A, Shepherd M, Frayling TM, Bulman MP, Ellard S, Froguel P, Hattersley AT. Pearson ER, et al. Among authors: stride a. Diabetes. 2001 Feb;50 Suppl 1:S101-7. doi: 10.2337/diabetes.50.2007.s101. Diabetes. 2001. PMID: 11272165

10

Clinical heterogeneity in monogenic diabetes caused by mutations in the glucokinase gene (GCK-MODY).

Cuesta-Muñoz AL, Tuomi T, Cobo-Vuilleumier N, Koskela H, Odili S, Stride A, Buettger C, Otonkoski T, Froguel P, Grimsby J, Garcia-Gimeno M, Matschinsky FM. Cuesta-Muñoz AL, et al. Among authors: stride a. Diabetes Care. 2010 Feb;33(2):290-2. doi: 10.2337/dc09-0681. Epub 2009 Nov 10. Diabetes Care. 2010. PMID: 19903754 Free PMC article.

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