Hattersley AT - Search Results

1

Prevalence of permanent neonatal diabetes in Slovakia and successful replacement of insulin with sulfonylurea therapy in KCNJ11 and ABCC8 mutation carriers.

Stanik J, Gasperikova D, Paskova M, Barak L, Javorkova J, Jancova E, Ciljakova M, Hlava P, Michalek J, Flanagan SE, Pearson E, Hattersley AT, Ellard S, Klimes I. Stanik J, et al. Among authors: hattersley at. J Clin Endocrinol Metab. 2007 Apr;92(4):1276-82. doi: 10.1210/jc.2006-2490. Epub 2007 Jan 9. J Clin Endocrinol Metab. 2007. PMID: 17213273 Free PMC article.

2

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

3

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.

4

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.

5

No evidence for linkage at candidate type 2 diabetes susceptibility loci on chromosomes 12 and 20 in United Kingdom Caucasians.

Frayling TM, McCarthy MI, Walker M, Levy JC, O'Rahilly S, Hitman GA, Rao PV, Bennett AJ, Jones EC, Menzel S, Ellard S, Hattersley AT. Frayling TM, et al. Among authors: hattersley at. J Clin Endocrinol Metab. 2000 Feb;85(2):853-7. doi: 10.1210/jcem.85.2.6395. J Clin Endocrinol Metab. 2000. PMID: 10690901

6

A high prevalence of glucokinase mutations in gestational diabetic subjects selected by clinical criteria.

Ellard S, Beards F, Allen LI, Shepherd M, Ballantyne E, Harvey R, Hattersley AT. Ellard S, et al. Among authors: hattersley at. Diabetologia. 2000 Feb;43(2):250-3. doi: 10.1007/s001250050038. Diabetologia. 2000. PMID: 10753050

7

Growth-hormone treatment and risk of diabetes.

Spyer G, Ellard S, Hattersley A. Spyer G, et al. Lancet. 2000 May 27;355(9218):1913-4. doi: 10.1016/S0140-6736(05)73362-6. Lancet. 2000. PMID: 10866472 No abstract available.

8

A severe clinical phenotype results from the co-inheritance of type 2 susceptibility genes and a hepatocyte nuclear factor-1alpha mutation.

Tack CJ, Ellard S, Hattersley AT. Tack CJ, et al. Among authors: hattersley at. Diabetes Care. 2000 Mar;23(3):424-5. doi: 10.2337/diacare.23.3.424. Diabetes Care. 2000. PMID: 10868881 No abstract available.

9

Sensitivity to sulphonylureas in patients with hepatocyte nuclear factor-1alpha gene mutations: evidence for pharmacogenetics in diabetes.

Pearson ER, Liddell WG, Shepherd M, Corrall RJ, Hattersley AT. Pearson ER, et al. Among authors: hattersley at. Diabet Med. 2000 Jul;17(7):543-5. doi: 10.1046/j.1464-5491.2000.00305.x. Diabet Med. 2000. PMID: 10972586

10

Proposed mechanism for a novel insertion/deletion frameshift mutation (I414G415ATCG-->CCA) in the hepatocyte nuclear factor 1 alpha (HNF-1 alpha) gene which causes maturity-onset diabetes of the young (MODY).

Ellard S, Bulman MP, Frayling TM, Shepherd M, Hattersley AT. Ellard S, et al. Among authors: hattersley at. Hum Mutat. 2000 Sep;16(3):273. doi: 10.1002/1098-1004(200009)16:3<273::AID-HUMU18>3.0.CO;2-Z. Hum Mutat. 2000. PMID: 10980542

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