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2003

Journal Article

Haplotype analysis of aldosterone synthase gene (CYP11B2) polymorphisms shows association with essential hypertension

Kumar, Natasha N., Benjafield, Adam V., Lin, Ruby C. Y., Wang, William Y. S., Stowasser, Michael and Morris, Brian J. (2003). Haplotype analysis of aldosterone synthase gene (CYP11B2) polymorphisms shows association with essential hypertension. Journal of Hypertension, 21 (7), 1331-1337. doi: 10.1097/HJH.0b013e328332031a

Haplotype analysis of aldosterone synthase gene (CYP11B2) polymorphisms shows association with essential hypertension

2002

Journal Article

A Randomised Controlled Trial of Medication Liaison Services: Acceptance and Use by Health Professionals

Stowasser, D., Collins, D.M. and Stowasser, M. (2002). A Randomised Controlled Trial of Medication Liaison Services: Acceptance and Use by Health Professionals. Journal of Pharmacy Practice & Research, 32 (3), 221-226. doi: 10.1002/jppr2002323221

A Randomised Controlled Trial of Medication Liaison Services: Acceptance and Use by Health Professionals

2002

Journal Article

Hyperaldosteronism: primary versus tertiary

Stowasser, M. (2002). Hyperaldosteronism: primary versus tertiary. Journal of Hypertension, 20 (1), 17-19. doi: 10.1097/00004872-200201000-00004

Hyperaldosteronism: primary versus tertiary

2002

Journal Article

The aldosterone-renin ratio and primary aldosteronism

Stowasser, M. and Gordon, R. D. (2002). The aldosterone-renin ratio and primary aldosteronism. Mayo Clinic Proceedings, 77 (2), 202-203.

The aldosterone-renin ratio and primary aldosteronism

2002

Journal Article

A Randomised Controlled Trial of Medication Liaison Services: Patient Outcomes

Stowasser, D., Collins, D. M. and Stowasser, M. (2002). A Randomised Controlled Trial of Medication Liaison Services: Patient Outcomes. Journal of Pharmacy Practice & Research, 32 (2), 133-140. doi: 10.1002/jppr2002322133

A Randomised Controlled Trial of Medication Liaison Services: Patient Outcomes

2001

Journal Article

Prevalence and diagnostic workup of primary aldosteronism: new knowledge and new approaches

Stowasser, Michael and Gordon, Richard D. (2001). Prevalence and diagnostic workup of primary aldosteronism: new knowledge and new approaches. Nephrology, 6 (3), 119-126. doi: 10.1046/j.1440-1797.2001.00040.x

Prevalence and diagnostic workup of primary aldosteronism: new knowledge and new approaches

2001

Journal Article

Primary aldosteronism: Revival of a syndrome

Stowasser, M. (2001). Primary aldosteronism: Revival of a syndrome. Journal of Hypertension, 19 (3), 363-366. doi: 10.1097/00004872-200103000-00002

Primary aldosteronism: Revival of a syndrome

2001

Journal Article

Polymorphisms of the renin-angiotensin system in patients with multifocal renal arterial fibromuscular dysplasia

Bofinger, A., Hawley, C., Fisher, P., Daunt, N., Stowasser, M. and Gordon, R. (2001). Polymorphisms of the renin-angiotensin system in patients with multifocal renal arterial fibromuscular dysplasia. Journal of Human Hypertension, 15 (3), 185-190. doi: 10.1038/sj.jhh.1001144

Polymorphisms of the renin-angiotensin system in patients with multifocal renal arterial fibromuscular dysplasia

2001

Journal Article

Familial varieties of primary aldosteronism

Stowasser, M, Gunasekera, TG and Gordon, RD (2001). Familial varieties of primary aldosteronism. Clinical And Experimental Pharmacology And Physiology, 28 (12), 1087-1090. doi: 10.1046/j.1440-1681.2001.03574.x

Familial varieties of primary aldosteronism

2001

Journal Article

New perspectives on the role of aldosterone excess in cardiovascular disease

Stowasser, M (2001). New perspectives on the role of aldosterone excess in cardiovascular disease. Clinical And Experimental Pharmacology And Physiology, 28 (10), 783-791. doi: 10.1046/j.1440-1681.2001.03523.x

New perspectives on the role of aldosterone excess in cardiovascular disease

2001

Journal Article

Primary aldosteronism: Rare bird or common cause of secondary hypertension?

Stowasser, M. (2001). Primary aldosteronism: Rare bird or common cause of secondary hypertension?. Current Hypertension Reports, 3 (3), 230-239.

Primary aldosteronism: Rare bird or common cause of secondary hypertension?

2001

Journal Article

Diagnosis and management of primary aldosteronism

Stowasser, M, Gordon, RD, Rutherford, JC, Nikwan, NZ, Daunt, N and Slater, GJ (2001). Diagnosis and management of primary aldosteronism. Journal of The Renin-angiotensin-aldosterone System, 2 (3), 156-169. doi: 10.3317/jraas.2001.022

Diagnosis and management of primary aldosteronism

2001

Journal Article

Primary aldosteronism: Are we diagnosing and operating on too few patients?

Gordon, RD, Stowasser, M and Rutherford, JC (2001). Primary aldosteronism: Are we diagnosing and operating on too few patients?. World Journal of Surgery, 25 (7), 941-947. doi: 10.1007/s00268-001-0033-4

Primary aldosteronism: Are we diagnosing and operating on too few patients?

2001

Journal Article

Familial hyperaldosteronism

Stowasser, Michael and Gordon, Richard D. (2001). Familial hyperaldosteronism. Journal of Steroid Biochemistry And Molecular Biology, 78 (3), 215-229. doi: 10.1016/S0960-0760(01)00097-8

Familial hyperaldosteronism

2000

Journal Article

Identifying Drug-Related Readmissions: Is There a Better Way of Assessing the Contribution of Adverse Medication Events?

Collins, D., Coombes, J., Staatz, C. E., Stowasser, D. and Stowasser, M. (2000). Identifying Drug-Related Readmissions: Is There a Better Way of Assessing the Contribution of Adverse Medication Events?. Australian Journal of Hospital Pharmacy, 30 (2), 47-52.

Identifying Drug-Related Readmissions: Is There a Better Way of Assessing the Contribution of Adverse Medication Events?

2000

Journal Article

Alpha-1-antitrypsin phenotypes in patients with renal arterial fibromuscular dysplasia

Bofinger, A., Hawley, C., Fisher, P., Daunt, N., Stowasser, M. and Gordon, Richard D. (2000). Alpha-1-antitrypsin phenotypes in patients with renal arterial fibromuscular dysplasia. Journal of Human Hypertension, 14 (2), 91-94.

Alpha-1-antitrypsin phenotypes in patients with renal arterial fibromuscular dysplasia

2000

Journal Article

Alpha-1-antitrypsin phenotypes in patients with renal arterial fibromuscular dysplasia

Bofinger, A., Hawley, C., Fisher, P., Daunt, N., Stowasser, M. and Gordon, R. (2000). Alpha-1-antitrypsin phenotypes in patients with renal arterial fibromuscular dysplasia. Journal of Human Hypertension, 14 (2), 91-94. doi: 10.1038/sj.jhh.1000935

Alpha-1-antitrypsin phenotypes in patients with renal arterial fibromuscular dysplasia

2000

Journal Article

Treatment of familial hyperaldosteronism type I: Only partial suppression of adrenocorticotropin required to correct hypertension

Stowasser, M., Bachmann, A. W., Huggard, P. R., Rossetti, T. R. and Gordon, R. D. (2000). Treatment of familial hyperaldosteronism type I: Only partial suppression of adrenocorticotropin required to correct hypertension. Journal of Clinical Endocrinology and Metabolism, 85 (9), 3313-3318. doi: 10.1210/jcem.85.9.6834

Treatment of familial hyperaldosteronism type I: Only partial suppression of adrenocorticotropin required to correct hypertension

2000

Journal Article

Sporadic and familial pheochromocytomas are associated with loss of at least two discrete intervals on chromosome 1p

Benn, DE, Dwight, T, Richardson, AL, Delbridge, L, Bambach, CP, Stowasser, M, Gordon, RD, Marsh, DJ and Robinson, BG (2000). Sporadic and familial pheochromocytomas are associated with loss of at least two discrete intervals on chromosome 1p. Cancer Research, 60 (24), 7048-7051.

Sporadic and familial pheochromocytomas are associated with loss of at least two discrete intervals on chromosome 1p

2000

Journal Article

Primary aldosteronism: learning from the study of familial varieties

Stowasser, M and Gordon, RD (2000). Primary aldosteronism: learning from the study of familial varieties. Journal of Hypertension, 18 (9), 1165-1176. doi: 10.1097/00004872-200018090-00002

Primary aldosteronism: learning from the study of familial varieties