نتایج جستجو برای: hyperaldosteronism

تعداد نتایج: 1682  

Journal: :The Journal of endocrinology 2015
Maria-Christina Zennaro Sheerazed Boulkroun Fabio Fernandes-Rosa

Primary aldosteronism (PA) is the most common and curable form of secondary hypertension. It is caused in the majority of cases by either unilateral aldosterone overproduction due to an aldosterone-producing adenoma (APA) or by bilateral adrenal hyperplasia. Recent advances in genome technology have allowed researchers to unravel part of the genetic abnormalities underlying the development of A...

2015

▼ Familial forms of primary aldosteronism have been suggested to account for up to 6 % of cases in referral centers. For many years, the genetics of familial hyperaldosteronism remained unknown, with the notable exception of glucocorticoid-remediable aldosteronism, due to unequal crossing over and formation of a chimeric 11β-hydroxylase/ aldosterone synthase gene. Over the past 5 years, mutatio...

Journal: :Journal of the American College of Surgeons 2010
Aarti Mathur Clinton D Kemp Utpal Dutta Smita Baid Alejandro Ayala Richard E Chang Seth M Steinberg Vasilios Papademetriou Eileen Lange Steven K Libutti James F Pingpank H Richard Alexander Giao Q Phan Marybeth Hughes W Marston Linehan Peter A Pinto Constantine A Stratakis Electron Kebebew

BACKGROUND In patients with primary hyperaldosteronism, distinguishing between unilateral and bilateral adrenal hypersecretion is critical in assessing treatment options. Adrenal venous sampling (AVS) has been advocated by some to be the gold standard for localization of the responsible lesion, but there remains a lack of consensus for the criteria and the standardization of technique. STUDY ...

Journal: :The Journal of clinical endocrinology and metabolism 2005
Sau-Cheung Tiu Cheung-Hei Choi Chi-Chung Shek Ying-Wai Ng Fredriech K W Chan Chiu-Ming Ng Alice P S Kong

Recent reviews recommended the use of the aldosterone/renin ratio (ARR) to screen for primary hyperaldosteronism. However, widely different cutoff levels have been proposed, and test characteristics of ARR under different conditions of sampling are not known. We conducted a retrospective review among 45 subjects with carefully validated diagnoses of primary hyperaldosteronism and 17 subjects wi...

2009
Panagiotis Kotsaftis Christos Savopoulos Dimitrios Agapakis George Ntaios Valentini Tzioufa Vasilios Papadopoulos Epaminondas Fahantidis Apostolos Hatzitolios

INTRODUCTION Primary hyperaldosteronism is only rarely caused by unilateral adrenal hyperplasia. CASE PRESENTATION A 73-year-old hypertensive Greek man (on 10 mg amlodipine for the last ten years) presented in the emergency department with severe muscle weakness of all limbs. The initial physical and laboratory examination revealed normal blood pressure, muscle weakness, severe hypokalemia, s...

2015

▼ Familial forms of primary aldosteronism have been suggested to account for up to 6 % of cases in referral centers. For many years, the genetics of familial hyperaldosteronism remained unknown, with the notable exception of glucocorticoid-remediable aldosteronism, due to unequal crossing over and formation of a chimeric 11β-hydroxylase/ aldosterone synthase gene. Over the past 5 years, mutatio...

Journal: :Hypertension 2010
Leonardo A Sechi Gianluca Colussi Cristiana Catena

Letters to the Editor will be published, if suitable, as space permits. They should not exceed 1000 words (typed double-spaced) in length and may be subject to editing or abridgment. To the Editor: In their prospective study, Gaddam et al 1 have examined the effects of spironolactone on cardiac structure in 34 patients with resistant hypertension who were separated according to their plasma ald...

Journal: :American journal of physiology. Renal physiology 2010
Stephanie S Fischer Daniela S Kempe Christina B Leibrock Rexhep Rexhepaj Balasaheb Siraskar Krishna M Boini Teresa F Ackermann Michael Föller Berthold Hocher Kevin P Rosenblatt Makoto Kuro-O Florian Lang

Klotho is a membrane protein participating in the inhibitory effect of FGF23 on the formation of 1,25-dihydroxyvitamin-D(3) [1,25(OH)(2)D(3)]. It participates in the regulation of renal tubular phosphate reabsorption and stimulates renal tubular Ca(2+) reabsorption. Klotho hypomorphic mice (klotho(hm)) suffer from severe growth deficit, rapid aging, and early death, events largely reversed by a...

2015

▼ Familial forms of primary aldosteronism have been suggested to account for up to 6 % of cases in referral centers. For many years, the genetics of familial hyperaldosteronism remained unknown, with the notable exception of glucocorticoid-remediable aldosteronism, due to unequal crossing over and formation of a chimeric 11β-hydroxylase/ aldosterone synthase gene. Over the past 5 years, mutatio...

Journal: :Circulation 2005
Matthias Sausbier Claudia Arntz Iancu Bucurenciu Hong Zhao Xiao-Bo Zhou Ulrike Sausbier Susanne Feil Simone Kamm Kyrill Essin Claudia A Sailer Usamah Abdullah Peter Krippeit-Drews Robert Feil Franz Hofmann Hans-Günther Knaus Chris Kenyon Michael J Shipston Johan F Storm Winfried Neuhuber Michael Korth Rudolf Schubert Maik Gollasch Peter Ruth

BACKGROUND Abnormally elevated blood pressure is the most prevalent risk factor for cardiovascular disease. The large-conductance, voltage- and Ca2+-dependent K+ (BK) channel has been proposed as an important effector in the control of vascular tone by linking membrane depolarization and local increases in cytosolic Ca2+ to hyperpolarizing K+ outward currents. However, the BK channel may also a...

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