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673 results
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Increased prevalence of proteinuria in diabetic sibs of proteinuric type 2 diabetic subjects.
Fava S, Azzopardi J, Hattersley AT, Watkins PJ. Fava S, et al. Among authors: hattersley at. Am J Kidney Dis. 2000 Apr;35(4):708-12. doi: 10.1016/s0272-6386(00)70019-9. Am J Kidney Dis. 2000. PMID: 10739793
Familial factors in diabetic nephropathy: an offspring study.
Agius E, Attard G, Shakespeare L, Clark P, Vidya MA, Hattersley AT, Fava S. Agius E, et al. Among authors: hattersley at. Diabet Med. 2006 Mar;23(3):331-4. doi: 10.1111/j.1464-5491.2006.01803.x. Diabet Med. 2006. PMID: 16492220
ACE gene polymorphism as a prognostic indicator in patients with type 2 diabetes and established renal disease.
Fava S, Azzopardi J, Ellard S, Hattersley AT. Fava S, et al. Among authors: hattersley at. Diabetes Care. 2001 Dec;24(12):2115-20. doi: 10.2337/diacare.24.12.2115. Diabetes Care. 2001. PMID: 11723093
Adult height and proteinuria in type 2 diabetes.
Fava S, Azzopardi J, Watkins PJ, Hattersley AT. Fava S, et al. Among authors: hattersley at. Nephrol Dial Transplant. 2001 Mar;16(3):525-8. doi: 10.1093/ndt/16.3.525. Nephrol Dial Transplant. 2001. PMID: 11239026
Evidence that single nucleotide polymorphism in the uncoupling protein 3 (UCP3) gene influences fat distribution in women of European and Asian origin.
Cassell PG, Saker PJ, Huxtable SJ, Kousta E, Jackson AE, Hattersley AT, Frayling TM, Walker M, Kopelman PG, Ramachandran A, Snehelatha C, Hitman GA, McCarthy MI. Cassell PG, et al. Among authors: hattersley at. Diabetologia. 2000 Dec;43(12):1558-64. doi: 10.1007/s001250051569. Diabetologia. 2000. PMID: 11151767
Reported parental age of death in type 2 diabetic patients with and without established diabetic nephropathy.
Fava S, Hattersley AT. Fava S, et al. Among authors: hattersley at. Eur J Intern Med. 2005 Nov;16(7):482-4. doi: 10.1016/j.ejim.2005.07.005. Eur J Intern Med. 2005. PMID: 16275540
The role of genetic susceptibility in diabetic nephropathy: evidence from family studies.
Fava S, Hattersley AT. Fava S, et al. Among authors: hattersley at. Nephrol Dial Transplant. 2002 Sep;17(9):1543-6. doi: 10.1093/ndt/17.9.1543. Nephrol Dial Transplant. 2002. PMID: 12198200 Review. No abstract available.
Severe hyperglycemia after renal transplantation in a pediatric patient with a mutation of the hepatocyte nuclear factor-1beta gene.
Waller SC, Rees L, Woolf AS, Ellard S, Pearson ER, Hattersley AT, Bingham C. Waller SC, et al. Among authors: hattersley at. Am J Kidney Dis. 2002 Dec;40(6):1325-30. doi: 10.1053/ajkd.2002.36915. Am J Kidney Dis. 2002. PMID: 12460054
UKPDS 21: low prevalence of the mitochondrial transfer RNA gene (tRNA(Leu(UUR))) mutation at position 3243bp in UK Caucasian type 2 diabetic patients.
Saker PJ, Hattersley AT, Barrow B, Hammersley MS, Horton V, Gillmer MD, Turner RC. Saker PJ, et al. Among authors: hattersley at. Diabet Med. 1997 Jan;14(1):42-5. doi: 10.1002/(SICI)1096-9136(199701)14:1<42::AID-DIA295>3.0.CO;2-T. Diabet Med. 1997. PMID: 9017352
Exocrine pancreatic dysfunction is common in hepatocyte nuclear factor 1β-associated renal disease and can be symptomatic.
Clissold RL, Fulford J, Hudson M, Shields BM, McDonald TJ, Ellard S, Hattersley AT, Bingham C. Clissold RL, et al. Among authors: hattersley at. Clin Kidney J. 2018 Aug;11(4):453-458. doi: 10.1093/ckj/sfx150. Epub 2018 Jan 30. Clin Kidney J. 2018. PMID: 30094008 Free PMC article.
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