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pro vyhledávání: '"Richard P, Lifton"'
Autor:
Cedric H.L. Shackleton, Richard P. Lifton, Michael Kashgarian, David S. Geller, Junhui Zhang, Max Wisgerhof
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 93:3117-3123
Primary aldosteronism is a leading cause of secondary hypertension (HTN), but the mechanisms underlying the characteristic renin-independent secretion of aldosterone remain unknown in most patients.We report a new familial form of aldosteronism in a
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 82:3570-3573
Glucocorticoid-remediable aldosteronism (GRA) is a rare form of inherited hypertension caused by a characteristic gene duplication. With the advent of definitive genetic testing for GRA, the performance of the traditional screening test for GRA, the
Autor:
Robert G. Dluhy, Richard P. Lifton, P. Silva, Francesco Fallo, W. R. Litchfield, Gordon H. Williams, C. Coolidge
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 82:1507-1510
Unlike other forms of primary aldosteronism, recent prospective studies have paradoxically revealed that glucocorticoid-remediable aldosteronism (GRA) is usually characterized by normal potassium (K+) levels. To evaluate this paradox we studied 10 GR
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 82:1071-1074
Liddle’s syndrome is an autosomal dominant form of hypertension that resembles primary hyperaldosteronism, is characterized by the early onset of hypertension with hypokalemia and suppression of both PRA and aldosterone, and is caused by mutations