Hattersley AT - Search Results

1

Molecular diagnostics in monogenic and multifactorial forms of type 2 diabetes.

McCarthy MI, Hattersley AT. McCarthy MI, et al. Among authors: hattersley at. Expert Rev Mol Diagn. 2001 Nov;1(4):403-12. doi: 10.1586/14737159.1.4.403. Expert Rev Mol Diagn. 2001. PMID: 11901855 Review.

2

Type II diabetes: clinical aspects of molecular biological studies.

Turner RC, Hattersley AT, Shaw JT, Levy JC. Turner RC, et al. Among authors: hattersley at. Diabetes. 1995 Jan;44(1):1-10. doi: 10.2337/diab.44.1.1. Diabetes. 1995. PMID: 7813802 Review.

3

Availability of type II diabetic families for detection of diabetes susceptibility genes.

Cook JT, Page RC, O'Rahilly S, Levy J, Holman R, Barrow B, Hattersley AT, Shaw AG, Wainscoat JS, Turner RC. Cook JT, et al. Among authors: hattersley at. Diabetes. 1993 Oct;42(10):1536-43. doi: 10.2337/diab.42.10.1536. Diabetes. 1993. PMID: 8375595

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

Allelic drop-out in exon 2 of the hepatocyte nuclear factor-1alpha gene hinders the identification of mutations in three families with maturity-onset diabetes of the young.

Ellard S, Bulman MP, Frayling TM, Allen LI, Dronsfield MJ, Tack CJ, Hattersley AT. Ellard S, et al. Among authors: hattersley at. Diabetes. 1999 Apr;48(4):921-3. doi: 10.2337/diabetes.48.4.921. Diabetes. 1999. PMID: 10102714 No abstract available.

8

The fetal insulin hypothesis: an alternative explanation of the association of low birthweight with diabetes and vascular disease.

Hattersley AT, Tooke JE. Hattersley AT, et al. Lancet. 1999 May 22;353(9166):1789-92. doi: 10.1016/S0140-6736(98)07546-1. Lancet. 1999. PMID: 10348008 Review.

9

Pigmentary retinal dystrophy and the syndrome of maternally inherited diabetes and deafness caused by the mitochondrial DNA 3243 tRNA(Leu) A to G mutation.

Smith PR, Bain SC, Good PA, Hattersley AT, Barnett AH, Gibson JM, Dodson PM. Smith PR, et al. Among authors: hattersley at. Ophthalmology. 1999 Jun;106(6):1101-8. doi: 10.1016/S0161-6420(99)90244-0. Ophthalmology. 1999. PMID: 10366077

10

Can molecular genetics help in the clinic?

Hattersley A. Hattersley A. Diabet Med. 1999 Sep;16(9):788-91. Diabet Med. 1999. PMID: 10510959 No abstract available.

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