Hattersley AT - Search Results

1

Permanent neonatal diabetes: different aetiology in Arabs compared to Europeans.

Habeb AM, Flanagan SE, Deeb A, Al-Alwan I, Alawneh H, Balafrej AA, Mutair A, Hattersley AT, Hussain K, Ellard S. Habeb AM, et al. Among authors: hattersley at. Arch Dis Child. 2012 Aug;97(8):721-3. doi: 10.1136/archdischild-2012-301744. Arch Dis Child. 2012. PMID: 22859427

2

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.

3

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.

4

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.

5

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.

6

R127W in HNF4alpha is a loss-of-function mutation causing maturity-onset diabetes of the young (MODY) in a UK Caucasian family.

Bulman MP, Ellard S, Hattersley AT. Bulman MP, et al. Among authors: hattersley at. Diabetologia. 2000 Sep;43(9):1203. doi: 10.1007/s001250051514. Diabetologia. 2000. PMID: 11043869 No abstract available.

7

Complete glucokinase deficiency is not a common cause of permanent neonatal diabetes.

Gloyn AL, Ellard S, Shield JP, Temple IK, Mackay DJ, Polak M, Barrett T, Hattersley AT. Gloyn AL, et al. Among authors: hattersley at. Diabetologia. 2002 Feb;45(2):290. doi: 10.1007/s00125-001-0746-9. Diabetologia. 2002. PMID: 11942315 No abstract available.

8

Heterogeneity in young adult onset diabetes: aetiology alters clinical characteristics.

Owen KR, Shepherd M, Stride A, Ellard S, Hattersley AT. Owen KR, et al. Among authors: hattersley at. Diabet Med. 2002 Sep;19(9):758-61. doi: 10.1046/j.1464-5491.2002.00766.x. Diabet Med. 2002. PMID: 12207813

9

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: hattersley at. Diabetes Care. 2003 Jul;26(7):2088-93. doi: 10.2337/diacare.26.7.2088. Diabetes Care. 2003. PMID: 12832318

10

Response to treatment with rosiglitazone in familial partial lipodystrophy due to a mutation in the LMNA gene.

Owen KR, Donohoe M, Ellard S, Hattersley AT. Owen KR, et al. Among authors: hattersley at. Diabet Med. 2003 Oct;20(10):823-7. doi: 10.1046/j.1464-5491.2003.01034.x. Diabet Med. 2003. PMID: 14510863

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