|
2008 Conference Publication Evidence for linkage of familial hyperaldosteronism type II at chromosome 7p22 in families from Australia, South America and ItalySukor, N., Mulatero, P., Gordon, R., So, A., Duffy, D., Bertello, C., Kelemen, L., Jeske, Y., Veglio, F. and Stowasser, M. (2008). Evidence for linkage of familial hyperaldosteronism type II at chromosome 7p22 in families from Australia, South America and Italy. 18th Annual Meeting of the European Society of Hypertension and 22nd Scientific Meeting of the International Society of Hypertension, Berlin, Germany, 14-19 June 2008. United States: Lippincott Williams & Wilkins. |
|
2008 Conference Publication Genotyping and expression studies of 7p22 candidate genes in familial hyperaldosteronism type IIJeske, Y.W., So, A., Kelemen, L., Sukor, N., Willys, C., Gordon, R.D., Duffy, D. and Stowasser, M. (2008). Genotyping and expression studies of 7p22 candidate genes in familial hyperaldosteronism type II. 29th Annual Scientific Meeting of the High Blood Pressure Research Council of Australia, Adelaide, Australia, 5-8 December 2007. United States: Lippincott Williams & Wilkins. doi: 10.1161/HYPERTENSIONAHA.108.009996 |
|
2007 Conference Publication Adrenal cortico-medullary interactions: pheochromocytoma-associated cortical hyperplasia and benign neoplasiaSukor, N., Stowasser, M., Rutherford, J., Nicol, D. L., Cohn, D. and Gordon, R. D. (2007). Adrenal cortico-medullary interactions: pheochromocytoma-associated cortical hyperplasia and benign neoplasia. 28th Annual Scientific Meeting of the High Blood Pressure Research Council of Australia, Brisbane, 7-8 December 2006. USA: American Heart Association. doi: 10.1161/HYPERTENSIONAHA.107.009421 |
|
2007 Conference Publication Rapid cortisol measurement aids in real-time confirmation of successful cannulation during adrenal venous samplingStowasser, M., Ward, G., Leggett, D., Cowley, D. and Gordon, R. (2007). Rapid cortisol measurement aids in real-time confirmation of successful cannulation during adrenal venous sampling. 17th European Meeting on Hypertension, Milan, Italy, 15-19 June 2007. PHILADELPHIA: LIPPINCOTT WILLIAMS & WILKINS. |
|
2007 Conference Publication Identification of individuals most likely to benefit from non-invasive central blood pressure monitoringSharman, J. E., Stowasser, M., Holland, D. J. and Marwick, T. H. (2007). Identification of individuals most likely to benefit from non-invasive central blood pressure monitoring. 28th Annual Scientific Meeting of the High Blood Pressure Research Council of Australia, Australia, 2006. Philadelphia, PA, U.S.A.: Lippincott Williams & Wilkins. doi: 10.1161/HYPERTENSIONAHA.107.009421 |
|
2007 Conference Publication Genetic basis of familial hyperaldosteronism type II: Further evidence of linkage at chromosome 7p22So, A, Jeske, Y., Gordon, R. D., Duffy, D., Kelemen, L., Bulmer, B. and Stowasser, M. (2007). Genetic basis of familial hyperaldosteronism type II: Further evidence of linkage at chromosome 7p22. 28th Annual Scientific Meeting of the High Blood Pressure Research Council of Australia, Brisbane, Australia, 7-8 December 2006. Baltimore, USA: Lippincott Williams & Wilkins for the American Heart Association. doi: 10.1161/HYPERTENSIONAHA.107.009421 |
|
2007 Conference Publication Can liquid chromatography-tandem mass spectrometry solve the problem of aldosterone measurement?Taylor, P., Carlton, L., Franklin, M., Cooper, D., Gordon, R.D. and Stowasser, M. (2007). Can liquid chromatography-tandem mass spectrometry solve the problem of aldosterone measurement?. 28th annual Scientific Meeting of the High Blood Pressure Research Council of Australia, Brisbane, 7-8 December, 2006. Philadelphia: Lippincott Williams & Wilkins. doi: 10.1161/HYPERTENSIONAHA.107.009421 |
|
2007 Conference Publication In hereditary hyperkalemic hypertension, genetic heterogeneity, salt intake and medications affet phenotype and delay diagnosis. Will genetic testing resolve this?Ku, Y., Stowasser, M., O'Shaughnessy, K. and Gordon, R. D. (2007). In hereditary hyperkalemic hypertension, genetic heterogeneity, salt intake and medications affet phenotype and delay diagnosis. Will genetic testing resolve this?. 28th Annual Scientific Meeting of the High Blood Pressure Research Council of Australia, Brisbane, 7-8 December 2006. Philadelphia, USA: Lippincott Williams & Wilkins. |
|
2007 Conference Publication Rapid cortisol measurement aids in real-time confirmation of successful cannulation during adrenal venous samplingsStowasser, M., Ward, G., Leggett, D., Cowley, D. and Gordon, R. (2007). Rapid cortisol measurement aids in real-time confirmation of successful cannulation during adrenal venous samplings. 17th European Meeting on Hypertension, Milan, Italy, 15th - 19th June, 2007. Philadelphia, USA: Lippincott Williams and Wilkins. |
|
2007 Conference Publication Examination of candidate genes at chromosome 7p22 in familial hyperaldosteronism type IIJeske, YW, So, A, Kelemen, L, Bulmer, B, Gordon, RD, Duffy, D and Stowasser, M (2007). Examination of candidate genes at chromosome 7p22 in familial hyperaldosteronism type II. 28th Annual Scientific Meeting of the High Blood Pressure Research Council of Australia, Brisbane, Australia, 7-8 December 2006. Baltimore, MD: Lippincott Williams & Wilkins for the American Heart Association. doi: 10.1161/HYPERTENSIONAHA.107.009421 |
|
2007 Conference Publication Cardiovascular effects of unilateral adrenalectomy are superior to those of aldosterone antagonist treatment in primary aldosteronismStowasser, Michael, Cowley, Diane, Gordon, Richard, Sharman, James and Marwick, Thomas (2007). Cardiovascular effects of unilateral adrenalectomy are superior to those of aldosterone antagonist treatment in primary aldosteronism. 2007 Scientific Sessions of the American Heart Association, Orlando, Florida, 3 - 7 November, 2007. Baltimore, MD.: Lippincott, Williams & Wilkins for the American Heart Association. |
|
2006 Conference Publication Prevalence of primary aldosteronism among Chinese hypertensive patientsGong, Y., Zhu, D., Zhang,, Chen, S. L., Chu, S.X., Zhang, L.H., Stowasser, M. and Gordon, R. D. (2006). Prevalence of primary aldosteronism among Chinese hypertensive patients. 21st Scientific Meeting of the International Society of Hypertension, Fukuoka, Japan, 15th to 19th October, 2006. Japan: International Society of Hypertension. |
|
2006 Conference Publication Lipoprotein (a) is elevated in patients with renovascular hypertension, but not in patients with primary aldosteronismKostner, K., Liu, Y., Cowley, D. and Stowasser, M. (2006). Lipoprotein (a) is elevated in patients with renovascular hypertension, but not in patients with primary aldosteronism. ISA 2006: XIV International Symposium on Atherosclerosis, Rome, Italy, 18-22 June 2006. E. Park, Shannon, Co. Clare, Ireland: Elsevier Ireland. doi: 10.1016/S1567-5688(06)81883-0 |
|
2006 Conference Publication The expanding role of aldosterone excess in cardiovascular diseaseStowasser, M., Sharman, J., Marwick, T. and Gordon, R. (2006). The expanding role of aldosterone excess in cardiovascular disease. 21sth Scientific Meeting of the International Society of Hypertension, 5th Asian Pacific Congress of Hypertension and 29th Annual Scientific Meeting of the Japanese Society of Hypertension, Fukuoka, Japan, 15-19 October 2006. United Kingdom: Lippincott Williams & Wilkins, Ltd.. |
|
2006 Conference Publication Further evidence of linkage at 7p22 with familial hyperaldosteronism type II and exclusion of genetic defects in the RBAK coding regionsSo, A., Jeske, Y., Gordon, R. D., Duffy, D. L., Bulmer, B. J. and Stowasser, M. (2006). Further evidence of linkage at 7p22 with familial hyperaldosteronism type II and exclusion of genetic defects in the RBAK coding regions. 27th Annual Scientific Meeting of the High Blood Pressure Research Council of Australia, Melbourne, Australia, 7-9 December, 2006. Oxford, UK: Blackwell. doi: 10.1111/j.1440-1681.2006.04428.x |
|
2006 Conference Publication No evidence of mutations in RBAK and PMS2 in association with familial hyperaldosteronism type IISo, A., Jeske, Y., Gordon, R. D., Duffy, D., Kelemen, L. and Stowasser, M. (2006). No evidence of mutations in RBAK and PMS2 in association with familial hyperaldosteronism type II. 21st Scientific Meeting of the International Society of Hypertension, Fukuoka, Japan, 15 to 19 October 2006. Japan: International Society of Hypertension. |
|
2005 Conference Publication Genomic structure of the human gene for protein kinase A regulatory subunit R1-beta (PRKAR1B) on 7p22: No evidence for mutations in familial hyperaldosteronism type II in a large affected kindredStowasser, M, Elphinstone, M, So, A, Jeske, Y and Gordon, R (2005). Genomic structure of the human gene for protein kinase A regulatory subunit R1-beta (PRKAR1B) on 7p22: No evidence for mutations in familial hyperaldosteronism type II in a large affected kindred. 26th Annual Scientific Meeting of the High-Blood-Pressure-Research-Council-of-Australia, Sydney Australia, Nov 24-26, 2004. OXFORD: BLACKWELL PUBLISHING. |
|
2005 Conference Publication Further evidence of linkage at 7p22 with familial hyperaldosteronism type IISo, Albertina, Stowasser, Michael, Gordon, Richard, Duffy, David and Jeske, Yvette (2005). Further evidence of linkage at 7p22 with familial hyperaldosteronism type II. 20th Annual Scientific Meeting of the American Society of Hypertension, San Francisco, USA, 14-18 May 2005. Elsevier Inc: New York, USA. doi: 10.1016/j.amjhyper.2005.03.659 |
|
2005 Conference Publication Familial hyperaldosteronism type II (FH-II): Further evidence for linkage at chromosome 7p22 but also for the predicted genetic heterogeneitySo, A., Stowasser, M., Gordon, R., Duffy, D. and Jeske, Y. (2005). Familial hyperaldosteronism type II (FH-II): Further evidence for linkage at chromosome 7p22 but also for the predicted genetic heterogeneity. The 26th Annual Scientific Meeting of the High Blood Pressure Research Council of Australia Inc., Sydney, Australia, 24-26 November, 2004. Blackwell Scientific Publications: BLACKWELL PUBLISHING. |
|
2005 Conference Publication No association between primary aldosteronism and two CYP11B2 polymorphisms in a well-characterized Australian sampleJeske, Y., So, A., Gordon, R. D., Duffy, D. and Stowasser, M. (2005). No association between primary aldosteronism and two CYP11B2 polymorphisms in a well-characterized Australian sample. 20th Annual Scientific Meeting of the American Society of Hypertension, San Francisco, U.S.A., 14-18 May 2005. New York, U.S.A.: Nature Publishing Group. doi: 10.1016/j.amjhyper.2005.03.012 |