Hattersley AT - Search Results

1

A genetic diagnosis of HNF1A diabetes alters treatment and improves glycaemic control in the majority of insulin-treated patients.

Shepherd M, Shields B, Ellard S, Rubio-Cabezas O, Hattersley AT. Shepherd M, et al. Among authors: hattersley at. Diabet Med. 2009 Apr;26(4):437-41. doi: 10.1111/j.1464-5491.2009.02690.x. Diabet Med. 2009. PMID: 19388975

2

Mutations in the hepatocyte nuclear factor-1alpha gene are a common cause of maturity-onset diabetes of the young in the U.K.

Frayling TM, Bulamn MP, Ellard S, Appleton M, Dronsfield MJ, Mackie AD, Baird JD, Kaisaki PJ, Yamagata K, Bell GI, Bain SC, Hattersley AT. Frayling TM, et al. Among authors: hattersley at. Diabetes. 1997 Apr;46(4):720-5. doi: 10.2337/diab.46.4.720. Diabetes. 1997. PMID: 9075818

3

A missense mutation in the hepatocyte nuclear factor 4 alpha gene in a UK pedigree with maturity-onset diabetes of the young.

Bulman MP, Dronsfield MJ, Frayling T, Appleton M, Bain SC, Ellard S, Hattersley AT. Bulman MP, et al. Among authors: hattersley at. Diabetologia. 1997 Jul;40(7):859-62. doi: 10.1007/s001250050760. Diabetologia. 1997. PMID: 9243109

4

A rapid screening method for hepatocyte nuclear factor 1 alpha frameshift mutations; prevalence in maturity-onset diabetes of the young and late-onset non-insulin dependent diabetes.

Frayling TM, Bulman MP, Appleton M, Hattersley AT, Ellard S. Frayling TM, et al. Among authors: hattersley at. Hum Genet. 1997 Dec;101(3):351-4. doi: 10.1007/s004390050640. Hum Genet. 1997. PMID: 9439666

5

The mitochondrial tRNA[Leu(UUR)] A to G 3243 mutation is associated with insulin-dependent and non-insulin-dependent diabetes in a Chinese population.

Smith PR, Dronsfield MJ, Mijovic CH, Hattersley AT, Yeung VT, Cockram C, Chan JC, Barnett AH, Bain SC. Smith PR, et al. Among authors: hattersley at. Diabet Med. 1997 Dec;14(12):1026-31. doi: 10.1002/(SICI)1096-9136(199712)14:12<1026::AID-DIA514>3.0.CO;2-M. Diabet Med. 1997. PMID: 9455929

6

Maturity-onset diabetes of the young: clinical heterogeneity explained by genetic heterogeneity.

Hattersley AT. Hattersley AT. Diabet Med. 1998 Jan;15(1):15-24. doi: 10.1002/(SICI)1096-9136(199801)15:1<15::AID-DIA562>3.0.CO;2-M. Diabet Med. 1998. PMID: 9472859 Review.

7

Mutations in hepatocyte nuclear factor 1beta are not a common cause of maturity-onset diabetes of the young in the U.K.

Beards F, Frayling T, Bulman M, Horikawa Y, Allen L, Appleton M, Bell GI, Ellard S, Hattersley AT. Beards F, et al. Among authors: hattersley at. Diabetes. 1998 Jul;47(7):1152-4. doi: 10.2337/diabetes.47.7.1152. Diabetes. 1998. PMID: 9648841 Review. No abstract available.

8

C282Y mutation in HFE (haemochromatosis) gene and type 2 diabetes.

Frayling T, Ellard S, Grove J, Walker M, Hattersley AT. Frayling T, et al. Among authors: hattersley at. Lancet. 1998 Jun 27;351(9120):1933-4. doi: 10.1016/S0140-6736(05)78618-9. Lancet. 1998. PMID: 9654270 No abstract available.

9

Mutations in the glucokinase gene of the fetus result in reduced birth weight.

Hattersley AT, Beards F, Ballantyne E, Appleton M, Harvey R, Ellard S. Hattersley AT, et al. Nat Genet. 1998 Jul;19(3):268-70. doi: 10.1038/953. Nat Genet. 1998. PMID: 9662401

10

Genetic testing for maturity onset diabetes of the young in childhood hyperglycaemia.

Matyka KA, Beards F, Appleton M, Ellard S, Hattersley A, Dunger DB. Matyka KA, et al. Arch Dis Child. 1998 Jun;78(6):552-4. doi: 10.1136/adc.78.6.552. Arch Dis Child. 1998. PMID: 9713013 Free PMC article.

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