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CD226 Gly307Ser association with multiple autoimmune diseases.
Published in:
Genes & Immunity, 2009, v. 10, n. 1, p. 5, doi. 10.1038/gene.2008.82
By:
- Hafler, J. P.;
- Maier, L. M.;
- Cooper, J. D.;
- Plagnol, V.;
- Hinks, A.;
- Simmonds, M. J.;
- Stevens, H. E.;
- Walker, N. M.;
- Healy, B.;
- Howson, J. M. M.;
- Maisuria, M.;
- Duley, S.;
- Coleman, G.;
- Gough, S. C. L.;
- Worthington, J.;
- Kuchroo, V. K.;
- Wicker, L. S.;
- Todd, J. A.
Publication type:
Article
Analysis of HLA class II genes in Hashimoto's thyroiditis reveals differences compared to Graves’ disease.
Published in:
Genes & Immunity, 2008, v. 9, n. 4, p. 358, doi. 10.1038/gene.2008.26
By:
- Zeitlin, A. A.;
- Heward, J. M.;
- Newby, P. R.;
- Carr-Smith, J. D.;
- Franklyn, J. A.;
- Gough, S. C. L.;
- Simmonds, M. J.
Publication type:
Article
Severe hypoglycaemia in adults with insulin-treated diabetes: impact on healthcare resources.
Published in:
Diabetic Medicine, 2016, v. 33, n. 4, p. 471, doi. 10.1111/dme.12844
By:
- Heller, S. R.;
- Frier, B. M.;
- Hersløv, M. L.;
- Gundgaard, J.;
- Gough, S. C. L.
Publication type:
Article
Pancreas transplantation: a treatment option for people with diabetes.
Published in:
Diabetic Medicine, 2014, v. 31, n. 5, p. 512, doi. 10.1111/dme.12373
By:
- Mittal, S.;
- Gough, S. C. L.
Publication type:
Article
Algorithm combining HbA<sub>1c</sub> and fasting plasma glucose for screening subjects for OGTT: Authors' response.
Published in:
2009
By:
- Manley, S. E.;
- Sikaris, K. A.;
- Lu, Z. X.;
- Nightingale, P. G.;
- Stratton, I. M.;
- Round, R. A.;
- Baskar, V.;
- Gough, S. C. L.
Publication type:
Letter
Validation of an algorithm combining haemoglobin A<sub>1c</sub> and fasting plasma glucose for diagnosis of diabetes mellitus in UK and Australian populations.
Published in:
Diabetic Medicine, 2009, v. 26, n. 2, p. 115, doi. 10.1111/j.1464-5491.2008.02652.x
By:
- Manley, S. E.;
- Sikaris, K. A.;
- Lu, Z. X.;
- Nightingale, P. G.;
- Stratton, I. M.;
- Round, R. A.;
- Baskar, V.;
- Gough, S. C. L.;
- Smith, J. M.
Publication type:
Article
Benefits of combination of insulin degludec and liraglutide are independent of baseline glycated haemoglobin level and duration of type 2 diabetes.
Published in:
Diabetes, Obesity & Metabolism, 2016, v. 18, n. 1, p. 40, doi. 10.1111/dom.12574
By:
- Rodbard, H. W.;
- Buse, J. B.;
- Woo, V.;
- Vilsbøll, T.;
- Langbakke, I. H.;
- Kvist, K.;
- Gough, S. C. L.
Publication type:
Article
One-year efficacy and safety of a fixed combination of insulin degludec and liraglutide in patients with type 2 diabetes: results of a 26-week extension to a 26-week main trial.
Published in:
Diabetes, Obesity & Metabolism, 2015, v. 17, n. 10, p. 965, doi. 10.1111/dom.12498
By:
- Gough, S. C. L.;
- Bode, B. W.;
- Woo, V. C.;
- Rodbard, H. W.;
- Linjawi, S.;
- Zacho, M.;
- Reiter, P. D.;
- Buse, J. B.
Publication type:
Article
Biosimilar insulins: a European perspective.
Published in:
Diabetes, Obesity & Metabolism, 2015, v. 17, n. 5, p. 445, doi. 10.1111/dom.12410
By:
- DeVries, J. H.;
- Gough, S. C. L.;
- Kiljanski, J.;
- Heinemann, L.
Publication type:
Article
Insulin degludec: overview of a novel ultra long-acting basal insulin.
Published in:
Diabetes, Obesity & Metabolism, 2013, v. 15, n. 4, p. 301, doi. 10.1111/dom.12052
By:
- Gough, S. C. L.;
- Harris, S.;
- Woo, V.;
- Davies, M.
Publication type:
Article
Hypoglycaemia risk with insulin degludec compared with insulin glargine in type 2 and type 1 diabetes: a pre-planned meta-analysis of phase 3 trials.
Published in:
Diabetes, Obesity & Metabolism, 2013, v. 15, n. 2, p. 175, doi. 10.1111/dom.12032
By:
- Ratner, R. E.;
- Gough, S. C. L.;
- Mathieu, C.;
- Del Prato, S.;
- Bode, B.;
- Mersebach, H.;
- Endahl, L.;
- Zinman, B.
Publication type:
Article
Liraglutide: from clinical trials to clinical practice.
Published in:
Diabetes, Obesity & Metabolism, 2012, v. 14, p. 33, doi. 10.1111/j.1463-1326.2012.01576.x
By:
- Gough, S. C. L.
Publication type:
Article
Mannose-binding lectin gene polymorphisms in a cohort study of ANCA-associated small vessel vasculitis.
Published in:
Rheumatology, 2007, v. 46, n. 7, p. 1076, doi. 10.1093/rheumatology/kem099
By:
- Kamesh, L.;
- Heward, J. M.;
- Williams, J. M.;
- Gough, S. C. L.;
- Savage, C. O. S.;
- Harper, L.
Publication type:
Article
Mannose-binding lectin gene polymorphisms in a cohort study of ANCA-associated small vessel vasculitis.
Published in:
Rheumatology, 2007, v. 46, n. 7, p. 1076, doi. 10.1093/rheumatology/kem099
By:
- L. Kamesh;
- J. M. Heward;
- J. M. Williams;
- S. C. L. Gough;
- C. O. S. Savage;
- L. Harper
Publication type:
Article
Contribution of Single Nucleotide Polymorphisms within FCRL3 and MAP3K7IP2 to the Pathogenesis of Graves’ Disease.
Published in:
Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 3, p. 1056, doi. 10.1210/jc.2005-1634
By:
- Simmonds, M. J.;
- Heward, J. M.;
- Carr-Smith, J.;
- Foxall, H.;
- Franklyn, J. A.;
- Gough, S. C. L.
Publication type:
Article
Common Allelic Variants of Exons 10, 12, and 33 of the Thyroglobulin Gene Are Not Associated with Autoimmune Thyroid Disease in the United Kingdom.
Published in:
Journal of Clinical Endocrinology & Metabolism, 2004, v. 89, n. 12, p. 6336, doi. 10.1210/jc.2004-1336
By:
- COLLINS, J. E.;
- HEWARD, J. M.;
- HOWSON, J. M. M.;
- FOXALL, H.;
- CARR-SMITH, J.;
- FRANKLYN, J. A.;
- GOUGH, S. C. L.
Publication type:
Article
Association of a Rare Thyroglobulin Gene Microsatellite Variant with Autoimmune Thyroid Disease.
Published in:
Journal of Clinical Endocrinology & Metabolism, 2003, v. 88, n. 10, p. 5039, doi. 10.1210/jc.2003-030093
By:
- COLLINS, J. E.;
- HEWARD, J. M.;
- CARR-SMITH, J.;
- DAYKIN, J.;
- FRANKLYN, J. A.;
- GOUGH, S. C. L.
Publication type:
Article
No Association of an Interleukin 4 Gene Promoter Polymorphism with Graves’ Disease in the United Kingdom.
Published in:
Journal of Clinical Endocrinology & Metabolism, 2001, v. 86, n. 8, p. 3861, doi. 10.1210/jc.86.8.3861
By:
- HEWARD, J. M.;
- NITHIYANANTHAN, R.;
- ALLAHABADIA, A.;
- GIBSON, S.;
- FRANKLYN, J. A.;
- GOUGH, S. C. L.
Publication type:
Article
A Heterozygous Deletion of the Autoimmune Regulator (AIRE1) Gene, Autoimmune Thyroid Disease, and Type 1 Diabetes: No Evidence for Association.
Published in:
Journal of Clinical Endocrinology & Metabolism, 2000, v. 85, n. 3, p. 1320, doi. 10.1210/jc.85.3.1320
By:
- NITHIYANANTHAN, R.;
- HEWARD, J. M.;
- ALLAHABADIA, A.;
- BARNETT, A. H.;
- FRANKLYN, J. A.;
- GOUGH, S. C. L.
Publication type:
Article
INS VNTR allelic variation and dynamic insulin secretion in healthy adult non-diabetic Caucasian subjects.
Published in:
Diabetic Medicine, 1999, v. 16, n. 11, p. 910, doi. 10.1046/j.1464-5491.1999.00169.x
By:
- Ahmed, S.;
- Bennett, S. T.;
- Huxtable, S. J.;
- Todd, J. A.;
- Matthews, D. R.;
- Gough, S. C. L.
Publication type:
Article
The Fibrinolytic System in Diabetes Mellitus.
Published in:
Diabetic Medicine, 1991, v. 8, n. 10, p. 898, doi. 10.1111/j.1464-5491.1991.tb01527.x
By:
- Gough, S. C. L.;
- Grant, P. J.
Publication type:
Article
Biphasic Insulin Aspart in Type 2 Diabetes Mellitus.
Published in:
Clinical Drug Investigation, 2007, v. 27, n. 5, p. 299, doi. 10.2165/00044011-200727050-00002
By:
- Gough, S. C. L.;
- Tibaldi, J.
Publication type:
Article
Genetic insights into disease mechanisms of autoimmunity.
Published in:
British Medical Bulletin, 2004, v. 71, n. 1, p. 93, doi. 10.1093/bmb/ldh032
By:
- Simmonds, M. J.;
- Gough, S. C. L.
Publication type:
Article
Safety and efficacy of liraglutide in patients with type 2 diabetes and elevated liver enzymes: individual patient data meta-analysis of the LEAD program.
Published in:
Alimentary Pharmacology & Therapeutics, 2013, v. 37, n. 2, p. 234, doi. 10.1111/apt.12149
By:
- Armstrong, M. J.;
- Houlihan, D. D.;
- Rowe, I. A.;
- Clausen, W. H. O.;
- Elbrønd, B.;
- Gough, S. C. L.;
- Tomlinson, J. W.;
- Newsome, P. N.
Publication type:
Article
Preliminary evidence for interaction of PTPN12 polymorphism with TSHR genotype and association with Graves’ ophthalmopathy.
Published in:
Clinical Endocrinology, 2007, v. 67, n. 5, p. 663, doi. 10.1111/j.1365-2265.2007.02942.x
By:
- Syed, A. A.;
- Simmonds, M. J.;
- Brand, O. J.;
- Franklyn, J. A.;
- Gough, S. C. L.;
- Heward, J. M.
Publication type:
Article
Tag SNP screening of the PDCD1 gene for association with Graves’ disease.
Published in:
Clinical Endocrinology, 2007, v. 67, n. 1, p. 125, doi. 10.1111/j.1365-2265.2007.02848.x
By:
- Newby, P. R.;
- Roberts-Davies, E. L.;
- Brand, O. J.;
- Heward, J. M.;
- Franklyn, J. A.;
- Gough, S. C. L.;
- Simmonds, M. J.
Publication type:
Article
Association of the BTNL2 rs2076530 single nucleotide polymorphism with Graves’ disease appears to be secondary to DRB1 exon 2 position β74.
Published in:
Clinical Endocrinology, 2006, v. 65, n. 4, p. 429, doi. 10.1111/j.1365-2265.2006.02586.x
By:
- Simmonds, M. J.;
- Heward, J. M.;
- Barrett, J. C.;
- Franklyn, J. A.;
- Gough, S. C. L.
Publication type:
Article
Use of Tag single nucleotide polymorphisms (SNPs) to screen PTPN21: no association with Graves’ disease.
Published in:
Clinical Endocrinology, 2006, v. 65, n. 3, p. 380, doi. 10.1111/j.1365-2265.2006.02608.x
By:
- Zeitlin, A. A.;
- Heward, J. M.;
- Brand, O. J.;
- Newby, P. R.;
- Franklyn, J. A.;
- Gough, S. C. L.;
- Simmonds, M. J.
Publication type:
Article
IL-13 and chromosome 5q31–q33: problems of identifying association within regions of linkage to Graves’ disease.
Published in:
2005
By:
- Simmonds, M. J.;
- Heward, J. M.;
- Franklyn, J. A.;
- Gough, S. C. L.
Publication type:
Letter
Lack of association of the vitamin D receptor gene with Graves’ disease in UK Caucasians.
Published in:
Clinical Endocrinology, 2004, v. 60, n. 5, p. 618, doi. 10.1111/j.1365-2265.2004.02015.x
By:
- Collins, J. E.;
- Heward, J. M.;
- Nithiyananthan, R.;
- Nejentsev, S.;
- Todd, J. A.;
- Franklyn, J. A.;
- Gough, S. C. L.
Publication type:
Article
Association of the large multifunctional proteasome (LMP2) gene with Graves' disease is a result of linkage disequilibrium with the HLA haplotype DRB1*0304-DQB1*02-DQA1*0501.
Published in:
Clinical Endocrinology, 1999, v. 51, n. 1, p. 115, doi. 10.1046/j.1365-2265.1999.00755.x
By:
- Heward;
- Allahabadia;
- Sheppard;
- Barnett;
- Franklyn;
- Gough;
- C. L. Gough, S.
Publication type:
Article

Found: 31

CD226 Gly307Ser association with multiple autoimmune diseases.

Analysis of HLA class II genes in Hashimoto's thyroiditis reveals differences compared to Graves’ disease.

Severe hypoglycaemia in adults with insulin-treated diabetes: impact on healthcare resources.

Pancreas transplantation: a treatment option for people with diabetes.

Algorithm combining HbA<sub>1c</sub> and fasting plasma glucose for screening subjects for OGTT: Authors' response.

Validation of an algorithm combining haemoglobin A<sub>1c</sub> and fasting plasma glucose for diagnosis of diabetes mellitus in UK and Australian populations.

Benefits of combination of insulin degludec and liraglutide are independent of baseline glycated haemoglobin level and duration of type 2 diabetes.

One-year efficacy and safety of a fixed combination of insulin degludec and liraglutide in patients with type 2 diabetes: results of a 26-week extension to a 26-week main trial.

Biosimilar insulins: a European perspective.

Insulin degludec: overview of a novel ultra long-acting basal insulin.

Hypoglycaemia risk with insulin degludec compared with insulin glargine in type 2 and type 1 diabetes: a pre-planned meta-analysis of phase 3 trials.

Liraglutide: from clinical trials to clinical practice.

Mannose-binding lectin gene polymorphisms in a cohort study of ANCA-associated small vessel vasculitis.

Mannose-binding lectin gene polymorphisms in a cohort study of ANCA-associated small vessel vasculitis.

Contribution of Single Nucleotide Polymorphisms within FCRL3 and MAP3K7IP2 to the Pathogenesis of Graves’ Disease.

Common Allelic Variants of Exons 10, 12, and 33 of the Thyroglobulin Gene Are Not Associated with Autoimmune Thyroid Disease in the United Kingdom.

Association of a Rare Thyroglobulin Gene Microsatellite Variant with Autoimmune Thyroid Disease.

No Association of an Interleukin 4 Gene Promoter Polymorphism with Graves’ Disease in the United Kingdom.

A Heterozygous Deletion of the Autoimmune Regulator (AIRE1) Gene, Autoimmune Thyroid Disease, and Type 1 Diabetes: No Evidence for Association.

INS VNTR allelic variation and dynamic insulin secretion in healthy adult non-diabetic Caucasian subjects.

The Fibrinolytic System in Diabetes Mellitus.

Biphasic Insulin Aspart in Type 2 Diabetes Mellitus.

Genetic insights into disease mechanisms of autoimmunity.

Safety and efficacy of liraglutide in patients with type 2 diabetes and elevated liver enzymes: individual patient data meta-analysis of the LEAD program.

Preliminary evidence for interaction of PTPN12 polymorphism with TSHR genotype and association with Graves’ ophthalmopathy.

Tag SNP screening of the PDCD1 gene for association with Graves’ disease.

Association of the BTNL2 rs2076530 single nucleotide polymorphism with Graves’ disease appears to be secondary to DRB1 exon 2 position β74.

Use of Tag single nucleotide polymorphisms (SNPs) to screen PTPN21: no association with Graves’ disease.

IL-13 and chromosome 5q31–q33: problems of identifying association within regions of linkage to Graves’ disease.

Lack of association of the vitamin D receptor gene with Graves’ disease in UK Caucasians.

Association of the large multifunctional proteasome (LMP2) gene with Graves' disease is a result of linkage disequilibrium with the HLA haplotype DRB10304-DQB102-DQA1*0501.