-
1
-
-
0014029230
-
Hypertension, increased aldosterone secretion, and low plasma renin activity relieved by dexamethasone
-
Sutherland DJ, Ruse JL, Laidlaw JC. Hypertension, increased aldosterone secretion, and low plasma renin activity relieved by dexamethasone. Can Med Assoc J 1966; 95: 1109-1119.
-
(1966)
Can Med Assoc J
, vol.95
, pp. 1109-1119
-
-
Sutherland, D.J.1
Ruse, J.L.2
Laidlaw, J.C.3
-
2
-
-
0014051406
-
A new form of congenital adrenal hyperplasia
-
New MI, Peterson RE. A new form of congenital adrenal hyperplasia. J Cin Endocrinol Metab 1967; 27: 300-305.
-
(1967)
J Cin Endocrinol Metab
, vol.27
, pp. 300-305
-
-
New, M.I.1
Peterson, R.E.2
-
3
-
-
0015605775
-
A kindred with familial glucocorticoid-suppressible hyperaldosteronism
-
Giebink GS et al. A kindred with familial glucocorticoid-suppressible hyperaldosteronism. J Clin Endocrinol Metab 1973; 36: 715-723.
-
(1973)
J Clin Endocrinol Metab
, vol.36
, pp. 715-723
-
-
Giebink, G.S.1
-
4
-
-
0018843347
-
Familial dexamethasone-suppressible normokalaemic hyperaldosteronism
-
Grim CE, Weinberger MH. Familial dexamethasone-suppressible normokalaemic hyperaldosteronism. Pediatrics 1980; 65: 597-604.
-
(1980)
Pediatrics
, vol.65
, pp. 597-604
-
-
Grim, C.E.1
Weinberger, M.H.2
-
5
-
-
0019748635
-
Genetic and pathophysiologic studies of a new kindred with glucocorticoid-suppressible hyperaldosteronism manifest in three generations
-
Ganguly A et al. Genetic and pathophysiologic studies of a new kindred with glucocorticoid-suppressible hyperaldosteronism manifest in three generations. J Clin Endocrinol Metab 1981; 53: 1041-1046.
-
(1981)
J Clin Endocrinol Metab
, vol.53
, pp. 1041-1046
-
-
Ganguly, A.1
-
6
-
-
0019757017
-
Overproduction of sodium-retaining steroids by the zona glomerulosa is adrenocorticotropin-dependent and mediates hypertension in dexamethasone-suppressible hyperaldosteronism
-
Gill JR, Bartter FC. Overproduction of sodium-retaining steroids by the zona glomerulosa is adrenocorticotropin-dependent and mediates hypertension in dexamethasone-suppressible hyperaldosteronism. J Clin Endocrinol Metab 1981; 53: 331-337.
-
(1981)
J Clin Endocrinol Metab
, vol.53
, pp. 331-337
-
-
Gill, J.R.1
Bartter, F.C.2
-
7
-
-
0020604139
-
The changing clincal spectrum of primary aldosteronism
-
Bravo E et al. The changing clincal spectrum of primary aldosteronism. Am J Med 1983; 74: 641-651.
-
(1983)
Am J Med
, vol.74
, pp. 641-651
-
-
Bravo, E.1
-
8
-
-
0021809836
-
A new family with dexamethasone suppressible hyperaldosteronism: Aldosterone unresponsiveness to angiotensin II
-
Fallo F et al. A new family with dexamethasone suppressible hyperaldosteronism: Aldosterone unresponsiveness to angiotensin II. Clin Endocrinol 1985; 22: 777-785.
-
(1985)
Clin Endocrinol
, vol.22
, pp. 777-785
-
-
Fallo, F.1
-
9
-
-
0003032786
-
Dexamethasone-suppressible hyperaldosteronism
-
Biglieri EG, Melby JC (eds). Raven Press: New York
-
Fallo F, Mantero F. Dexamethasone-suppressible hyperaldosteronism. In: Biglieri EG, Melby JC (eds). Endocrine hypertension. Raven Press: New York, 1990, pp 87-97.
-
(1990)
Endocrine Hypertension
, pp. 87-97
-
-
Fallo, F.1
Mantero, F.2
-
10
-
-
0027052962
-
Glucocorticoid-remediable aldosteronism in a large kindred: Clinical spectrum and diagnosis using a characteristic biochemical phenotype
-
Rich GM et al. Glucocorticoid-remediable aldosteronism in a large kindred: clinical spectrum and diagnosis using a characteristic biochemical phenotype. Annal Intern Med 1992; 116: 813-820.
-
(1992)
Annal Intern Med
, vol.116
, pp. 813-820
-
-
Rich, G.M.1
-
11
-
-
0019757480
-
Adrenal glomerulosa function in patients with dexamethasone-suppressible hyperaldosteronism
-
Oberfield SE et al. Adrenal glomerulosa function in patients with dexamethasone-suppressible hyperaldosteronism. J Clin Endocrinol Metab 1981; 53: 158-1664.
-
(1981)
J Clin Endocrinol Metab
, vol.53
, pp. 158-1664
-
-
Oberfield, S.E.1
-
12
-
-
6844221127
-
Glucocorticoid-suppressible hyperaldosteronism: Steroid and body electrolyte measurements and responses to angiotensin II and adrenocorticotropin
-
Mantero F, Biglieri EG, Funder JW (eds). Raven Press: New York
-
Connell JMC et al. Glucocorticoid-suppressible hyperaldosteronism: Steroid and body electrolyte measurements and responses to angiotensin II and adrenocorticotropin. In: Mantero F, Biglieri EG, Funder JW (eds). The Adrenal Gland and Hypertension. Raven Press: New York, 1985, pp 405-420.
-
(1985)
The Adrenal Gland and Hypertension
, pp. 405-420
-
-
Connell, J.M.C.1
-
13
-
-
0021151940
-
Adrenal steroid response to ACTH in glucocorticoid-suppressible hyperaldosteronism
-
Ganguly A et al. Adrenal steroid response to ACTH in glucocorticoid-suppressible hyperaldosteronism. Hypertension 1984; 6: 563-566.
-
(1984)
Hypertension
, vol.6
, pp. 563-566
-
-
Ganguly, A.1
-
14
-
-
0018166761
-
Mineralocorticoids, salt balance, and blood pressure after prolonged ACTH administration in juvenile hypertension
-
Rauh W et al. Mineralocorticoids, salt balance, and blood pressure after prolonged ACTH administration in juvenile hypertension. Klin Wochenschr 1978; 56: 161-168.
-
(1978)
Klin Wochenschr
, vol.56
, pp. 161-168
-
-
Rauh, W.1
-
15
-
-
0028883357
-
Glucocorticoid-suppressible hyperaldosteronism and adrenal tumours in a single french pedigree
-
Pascoe L et al. Glucocorticoid-suppressible hyperaldosteronism and adrenal tumours in a single french pedigree. J Clin Invest 1995; 96: 2236-2246.
-
(1995)
J Clin Invest
, vol.96
, pp. 2236-2246
-
-
Pascoe, L.1
-
16
-
-
0022346884
-
Hypertension corrected and aldosterone responsiveness to renin-angiotensin restored by long-term dexamethasone in glucocorticoid-suppressible hyperaldosteronism
-
Woodland E et al. Hypertension corrected and aldosterone responsiveness to renin-angiotensin restored by long-term dexamethasone in glucocorticoid-suppressible hyperaldosteronism. Clin Exp Pharmacol Physiol 1985; 12: 245-248.
-
(1985)
Clin Exp Pharmacol Physiol
, vol.12
, pp. 245-248
-
-
Woodland, E.1
-
17
-
-
0021171686
-
Elevated urinary excretion of 18-oxocortisol in glucocorticoid-suppressible hyperaldosteronism
-
Gomez-Sanchez CE et al. Elevated urinary excretion of 18-oxocortisol in glucocorticoid-suppressible hyperaldosteronism. J Clin Endocrinol Metab 1984; 59: 1022-1024.
-
(1984)
J Clin Endocrinol Metab
, vol.59
, pp. 1022-1024
-
-
Gomez-Sanchez, C.E.1
-
18
-
-
0025006193
-
Defective fasciculata zone function as the mechanism of glucocorticoid-remediable aldosteronism
-
Ulick S et al. Defective fasciculata zone function as the mechanism of glucocorticoid-remediable aldosteronism. J Clin Endocrinol Metab 1990; 71: 1151-1157.
-
(1990)
J Clin Endocrinol Metab
, vol.71
, pp. 1151-1157
-
-
Ulick, S.1
-
19
-
-
0023784309
-
Dexamethasone-suppressible hyperaldosteronism: Studies on overproduction of 18-hydroxycortisol in three affected family members
-
Davies JRE et al. Dexamethasone-suppressible hyperaldosteronism: Studies on overproduction of 18-hydroxycortisol in three affected family members. Clin Endocrinol 1988; 29: 297-308.
-
(1988)
Clin Endocrinol
, vol.29
, pp. 297-308
-
-
Davies, J.R.E.1
-
20
-
-
0026919361
-
Hereditary hypertension caused by chiameric gene duplications and ectopic expression of aldosterone synthase
-
Lifton RP et al. Hereditary hypertension caused by chiameric gene duplications and ectopic expression of aldosterone synthase. Nat Genet 1992; 2: 66-74.
-
(1992)
Nat Genet
, vol.2
, pp. 66-74
-
-
Lifton, R.P.1
-
21
-
-
0026580019
-
A chimaeric 11β-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable hyperaldosteronism and human hypertension
-
Lifton RP et al. A chimaeric 11β-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable hyperaldosteronism and human hypertension. Nature 1992; 355: 262-265.
-
(1992)
Nature
, vol.355
, pp. 262-265
-
-
Lifton, R.P.1
-
22
-
-
0023433512
-
Cloning of cDNA encoding steroid 11-hydroxylase (P450 c11)
-
Chua SC et al. Cloning of cDNA encoding steroid 11-hydroxylase (P450 c11). Proc Natl Acad Sci USA 1987; 84: 7193-7197.
-
(1987)
Proc Natl Acad Sci USA
, vol.84
, pp. 7193-7197
-
-
Chua, S.C.1
-
23
-
-
0024842845
-
Characterization of two genes encoding human steroid 11β-hydroxylase (P-450 11β)
-
Mornet E, Dupont B, Vitek A, White PC. Characterization of two genes encoding human steroid 11β-hydroxylase (P-450 11β). J Biol Chem 1989; 264: 20961-20967.
-
(1989)
J Biol Chem
, vol.264
, pp. 20961-20967
-
-
Mornet, E.1
Dupont, B.2
Vitek, A.3
White, P.C.4
-
24
-
-
0026543213
-
Role of steroid 11β-hydroxylase and steroid 18-hydroxylase in the biosynthesis of glucocorticoids and mineralocorticoids in humans
-
Kawamoto T et al. Role of steroid 11β-hydroxylase and steroid 18-hydroxylase in the biosynthesis of glucocorticoids and mineralocorticoids in humans. Proc Natl Acad Sci USA 1992; 89: 1458-1462.
-
(1992)
Proc Natl Acad Sci USA
, vol.89
, pp. 1458-1462
-
-
Kawamoto, T.1
-
25
-
-
0026701168
-
Glucocorticoid-suppressible hyperaldosteronism results from hybrid genes created by unequal crossovers between CYP11B1 and CYP11B2
-
Pascoe L et al. Glucocorticoid-suppressible hyperaldosteronism results from hybrid genes created by unequal crossovers between CYP11B1 and CYP11B2, Proc Natl Acad Sci USA 1992; 89: 8327-8331.
-
(1992)
Proc Natl Acad Sci USA
, vol.89
, pp. 8327-8331
-
-
Pascoe, L.1
-
26
-
-
0028136752
-
Rapid diagnosis of glucocorticoid-suppressible hyperaldosteronism in infants and adolescents
-
Jamieson A et al. Rapid diagnosis of glucocorticoid-suppressible hyperaldosteronism in infants and adolescents. Arch Dis Child 1994; 71: 40-43.
-
(1994)
Arch Dis Child
, vol.71
, pp. 40-43
-
-
Jamieson, A.1
-
27
-
-
0029617775
-
Clinical, biochemical and genetic approaches to the detection of familial hyperaldosteronism type I
-
Stowasser M et al. Clinical, biochemical and genetic approaches to the detection of familial hyperaldosteronism type I. J Hypertens 1995; 13: 1610-1613,
-
(1995)
J Hypertens
, vol.13
, pp. 1610-1613
-
-
Stowasser, M.1
-
28
-
-
0029042995
-
Glucocorticoid-suppressible hyperaldosteronism: Effects of cross-over site and parental origin of chimaeric gene
-
Jamieson A et al. Glucocorticoid-suppressible hyperaldosteronism: effects of cross-over site and parental origin of chimaeric gene. Clin Sci 1995; 88: 563-570.
-
(1995)
Clin Sci
, vol.88
, pp. 563-570
-
-
Jamieson, A.1
-
29
-
-
0023118840
-
Long-term evolution of glucocorticoid suppressible hyperaldosteronism
-
Stockigt JR, Scoggins BA. Long-term evolution of glucocorticoid suppressible hyperaldosteronism. J Clin Endocrinol Metab 1987; 64: 22-26.
-
(1987)
J Clin Endocrinol Metab
, vol.64
, pp. 22-26
-
-
Stockigt, J.R.1
Scoggins, B.A.2
-
30
-
-
0001182641
-
A familial renal disorder simulating primary aldosteronism but with negligible aldosterone secretion
-
Liddle GW, Bledsoe T, Coppage WS. A familial renal disorder simulating primary aldosteronism but with negligible aldosterone secretion. Trans Assoc Phys 1963; 76: 199-213.
-
(1963)
Trans Assoc Phys
, vol.76
, pp. 199-213
-
-
Liddle, G.W.1
Bledsoe, T.2
Coppage, W.S.3
-
31
-
-
0019750222
-
The effect of triamterene and sodium intake on renin, aldosterone and erythrocyte sodium transport in Liddle's syndrome
-
Wang C et al. The effect of triamterene and sodium intake on renin, aldosterone and erythrocyte sodium transport in Liddle's syndrome. J Clin Endocrinol Metab 1981; 52: 1027-1032.
-
(1981)
J Clin Endocrinol Metab
, vol.52
, pp. 1027-1032
-
-
Wang, C.1
-
32
-
-
0023157314
-
Liddle's syndrome, an uncommon form of hyporeninaemic hypoaldosteronism: Functional and histopathological studies
-
Nakada T et al. Liddle's syndrome, an uncommon form of hyporeninaemic hypoaldosteronism: functional and histopathological studies. J Urol 1987; 137: 636-640.
-
(1987)
J Urol
, vol.137
, pp. 636-640
-
-
Nakada, T.1
-
33
-
-
0028154726
-
Brief report: Liddle's syndrome revisited - A disorder of sodium reabsorption in the distal tubule
-
Botero-Valez M, Curtis JJ, Warnock DG. Brief report: Liddle's syndrome revisited - a disorder of sodium reabsorption in the distal tubule. N Eng J Med 1994; 330: 178-181.
-
(1994)
N Eng J Med
, vol.330
, pp. 178-181
-
-
Botero-Valez, M.1
Curtis, J.J.2
Warnock, D.G.3
-
35
-
-
0027946089
-
Liddle's syndrome: Heritable human hypertension caused by mutations in the β-subunit of the epithelial sodium channel
-
Shimkets RA et al. Liddle's syndrome: heritable human hypertension caused by mutations in the β-subunit of the epithelial sodium channel. Cell 1994; 79: 407-414.
-
(1994)
Cell
, vol.79
, pp. 407-414
-
-
Shimkets, R.A.1
-
36
-
-
0029092801
-
Hypertension caused by a truncated epithelial sodium channel gamma subunit: Genetic heterogeneity of Liddle syndrome
-
Hansson JH et al. Hypertension caused by a truncated epithelial sodium channel gamma subunit: genetic heterogeneity of Liddle syndrome. Nat Genet 1995; 11: 76-82.
-
(1995)
Nat Genet
, vol.11
, pp. 76-82
-
-
Hansson, J.H.1
-
37
-
-
0029591506
-
Mechanism by which Liddle's syndrome mutations increase activity of a human epithelial sodium channel
-
Snyder PM et al. Mechanism by which Liddle's syndrome mutations increase activity of a human epithelial sodium channel. Cell 1995; 83: 969-978.
-
(1995)
Cell
, vol.83
, pp. 969-978
-
-
Snyder, P.M.1
-
38
-
-
0018598286
-
A syndrome of apparent mineralocorticoid excess associated with defects in the peripheral metabolism of cortisol
-
Ulick S et al. A syndrome of apparent mineralocorticoid excess associated with defects in the peripheral metabolism of cortisol. J Clin Endocrinol Metab 1979; 49: 757-764.
-
(1979)
J Clin Endocrinol Metab
, vol.49
, pp. 757-764
-
-
Ulick, S.1
-
39
-
-
0001002616
-
The hypertension of apparent mineralocorticoid excess (AME) syndrome
-
Biglieri EG, Melby JE (eds). Raven Press Ltd: New York
-
Shackleton CHL, Stewart PM. The hypertension of apparent mineralocorticoid excess (AME) syndrome. In: Biglieri EG, Melby JE (eds). Endocrine Hypertension. 1990, Raven Press Ltd: New York, pp 155-173.
-
(1990)
Endocrine Hypertension
, pp. 155-173
-
-
Shackleton, C.H.L.1
Stewart, P.M.2
-
40
-
-
0018931866
-
Hypertension in a four-year-old child: Gas chromatographic and mass spectrometric evidence for deficient hepatic metabolism of steroids
-
Shackleton CHL et al. Hypertension in a four-year-old child: gas chromatographic and mass spectrometric evidence for deficient hepatic metabolism of steroids. J Clin Endocrinol Metab 1980; 50: 786-792.
-
(1980)
J Clin Endocrinol Metab
, vol.50
, pp. 786-792
-
-
Shackleton, C.H.L.1
-
41
-
-
0021883201
-
Congenital 11β-hydroxysteroid dehydrogenase deficiency associated with juvenile hypertension. Corticosteroid metabolite profiles of four patients and their families
-
Shackleton CHL et al. Congenital 11β-hydroxysteroid dehydrogenase deficiency associated with juvenile hypertension. Corticosteroid metabolite profiles of four patients and their families. Clin Endocrinol 1985; 22: 701-712.
-
(1985)
Clin Endocrinol
, vol.22
, pp. 701-712
-
-
Shackleton, C.H.L.1
-
42
-
-
0022489562
-
The syndrome of apparent mineralocorticoid excess: Its association with 11β-dehydrogenase and 5β-reductase deficiency and some consequences for corticosteroid metabolism
-
Monder C et al. The syndrome of apparent mineralocorticoid excess: its association with 11β-dehydrogenase and 5β-reductase deficiency and some consequences for corticosteroid metabolism. J Clin Endocrinol Metab 1986; 63: 550-557.
-
(1986)
J Clin Endocrinol Metab
, vol.63
, pp. 550-557
-
-
Monder, C.1
-
43
-
-
85047677780
-
Fatal, lowrenin hypertension associated with a disturbance of cortisol metabolism
-
Honour JW, Dillon MJ, Levin M, Shah V. Fatal, lowrenin hypertension associated with a disturbance of cortisol metabolism. Arch Dis Child 1983; 58: 1018-1020.
-
(1983)
Arch Dis Child
, vol.58
, pp. 1018-1020
-
-
Honour, J.W.1
Dillon, M.J.2
Levin, M.3
Shah, V.4
-
44
-
-
0023760499
-
Syndrome of apparent mineralocorticoid excess: A defect in the cortisol - Cortisone shuttle
-
Stewart PM, Corrie JET, Shackleton CHL, Edwards CRW. Syndrome of apparent mineralocorticoid excess: A defect in the cortisol - cortisone shuttle. J Clin Invest 1988; 82: 340-349.
-
(1988)
J Clin Invest
, vol.82
, pp. 340-349
-
-
Stewart, P.M.1
Corrie, J.E.T.2
Shackleton, C.H.L.3
Edwards, C.R.W.4
-
45
-
-
0023236388
-
New findings in apparent mineralocorticoid excess
-
Dimartino-Nardi J et al. New findings in apparent mineralocorticoid excess. Clin Endocrinol 1988; 27: 49-62.
-
(1988)
Clin Endocrinol
, vol.27
, pp. 49-62
-
-
Dimartino-Nardi, J.1
-
46
-
-
2642594165
-
Mineralocorticoid activity of liquorice: 11β-hydroxysteroid dehydrogenase comes of age
-
Stewart PM et al. Mineralocorticoid activity of liquorice: 11β-hydroxysteroid dehydrogenase comes of age. Lancet 1987; i: 1208-1210.
-
(1987)
Lancet
, vol.1
, pp. 1208-1210
-
-
Stewart, P.M.1
-
47
-
-
0025176537
-
Mineralocorticoid activity of carbenoxolone: Contrasting effects of carbenoxolone and liquorice on 11β-hydroxysteroid dehydrogenase activity in man
-
Stewart PM et al. Mineralocorticoid activity of carbenoxolone: Contrasting effects of carbenoxolone and liquorice on 11β-hydroxysteroid dehydrogenase activity in man. Clin Sci 1990; 78: 49-54.
-
(1990)
Clin Sci
, vol.78
, pp. 49-54
-
-
Stewart, P.M.1
-
48
-
-
0024597923
-
The antinatriuretic and kaluretic effects of the glucocorticoids corticosterone and cortisol following pre-treatment with carbenoxolone sodium (a liquorice derivative) in the adrenalectomized rat
-
Souness GW, Morris DJ. The antinatriuretic and kaluretic effects of the glucocorticoids corticosterone and cortisol following pre-treatment with carbenoxolone sodium (a liquorice derivative) in the adrenalectomized rat. Endocrinology 1989; 124: 1588-1590.
-
(1989)
Endocrinology
, vol.124
, pp. 1588-1590
-
-
Souness, G.W.1
Morris, D.J.2
-
49
-
-
0025989937
-
Licorice-induced hypermineralocorticoidism
-
Farese RV et al. Licorice-induced hypermineralocorticoidism. N Engl J Med 1991; 325: 1225-1227.
-
(1991)
N Engl J Med
, vol.325
, pp. 1225-1227
-
-
Farese, R.V.1
-
50
-
-
0023221667
-
Cloning of human mineralocorticoid receptor complementary DNA: Structural and functional kinship with the glucocorticoid receptor
-
Arriza JL et al. Cloning of human mineralocorticoid receptor complementary DNA: Structural and functional kinship with the glucocorticoid receptor. Science 1987; 237: 268-275.
-
(1987)
Science
, vol.237
, pp. 268-275
-
-
Arriza, J.L.1
-
51
-
-
2542624590
-
Renal mineralocorticoid receptors and hippocampal corticosterone-binding species have identical intrinsic steroid specificity
-
Krozowski K, Funder JW. Renal mineralocorticoid receptors and hippocampal corticosterone-binding species have identical intrinsic steroid specificity. Proc Natl Acad Sci USA, 1983; 80: 6056-6060.
-
(1983)
Proc Natl Acad Sci USA
, vol.80
, pp. 6056-6060
-
-
Krozowski, K.1
Funder, J.W.2
-
52
-
-
0023761690
-
Localisation of 11β-hydroxysteroid dehydrogenase-tissue specific protector of the mineralocorticoid receptor
-
Edwards CRW et al. Localisation of 11β-hydroxysteroid dehydrogenase-tissue specific protector of the mineralocorticoid receptor. Lancet 1988; ii: 986-989.
-
(1988)
Lancet
, vol.2
, pp. 986-989
-
-
Edwards, C.R.W.1
-
53
-
-
0023743171
-
Mineral-ocorticoid action: Target tissue specificity is enzyme, not receptor, mediated
-
Funder JW, Pearce PT, Smith R, Smith AI. Mineral-ocorticoid action: target tissue specificity is enzyme, not receptor, mediated. Science 1988; 242: 583-585.
-
(1988)
Science
, vol.242
, pp. 583-585
-
-
Funder, J.W.1
Pearce, P.T.2
Smith, R.3
Smith, A.I.4
-
54
-
-
0026095840
-
The human gene for 11β-hydroxysteroid dehydrogenase. Structure, tissue distribution, and chromosomal localization
-
Tannin GM et al. The human gene for 11β-hydroxysteroid dehydrogenase. Structure, tissue distribution, and chromosomal localization. J Biol Chem 1991; 266: 16653-16658.
-
(1991)
J Biol Chem
, vol.266
, pp. 16653-16658
-
-
Tannin, G.M.1
-
55
-
-
0027159080
-
Human placental 11β-hydroxysteroid dehydrogenase: Evidence for and partial purification of a distinct NAD-dependent isoform
-
Brown RW, Chapman KE, Edwards CRW, Seckl JR. Human placental 11β-hydroxysteroid dehydrogenase: Evidence for and partial purification of a distinct NAD-dependent isoform. Endocrinology 1993; 132: 2614-2621.
-
(1993)
Endocrinology
, vol.132
, pp. 2614-2621
-
-
Brown, R.W.1
Chapman, K.E.2
Edwards, C.R.W.3
Seckl, J.R.4
-
58
-
-
0029095113
-
Gene structure and chromosomal localization of the human D11K gene encoding the kidney (type 2) isozyme of 11β-hydroxysteroid dehydrogenase
-
Agarwal AK, Rogerson FM, Mune T, White PC. Gene structure and chromosomal localization of the human D11K gene encoding the kidney (type 2) isozyme of 11β-hydroxysteroid dehydrogenase. Genomics 1995; 29: 195-199.
-
(1995)
Genomics
, vol.29
, pp. 195-199
-
-
Agarwal, A.K.1
Rogerson, F.M.2
Mune, T.3
White, P.C.4
-
59
-
-
0029060080
-
A mutation in the HSD11B2 gene in a family with apparent mineralocorticoid excess
-
Wilson RC et al. A mutation in the HSD11B2 gene in a family with apparent mineralocorticoid excess. J Clin Endocrinol Metab 1995; 80: 2263-2266.
-
(1995)
J Clin Endocrinol Metab
, vol.80
, pp. 2263-2266
-
-
Wilson, R.C.1
-
60
-
-
0029160972
-
Human hyypertension caused by mutations in the kidney isozyme of 11β-hydroxysteroid dehydrogenase
-
Mune T et al. Human hyypertension caused by mutations in the kidney isozyme of 11β-hydroxysteroid dehydrogenase. Nat Genet 1995; 10: 394-399.
-
(1995)
Nat Genet
, vol.10
, pp. 394-399
-
-
Mune, T.1
-
61
-
-
0030049329
-
Human hypertension in the syndrome of apparent mineralocorticoid excess due to mutation of the type 2 11β-hydioxysteroid dehydrogenase gene
-
Stewart PM et al. Human hypertension in the syndrome of apparent mineralocorticoid excess due to mutation of the type 2 11β-hydioxysteroid dehydrogenase gene. Lancet 1996; 347: 88-91.
-
(1996)
Lancet
, vol.347
, pp. 88-91
-
-
Stewart, P.M.1
-
62
-
-
0031046241
-
11β-hydroxysteroid dehydrogenase and the syndrome of apparent mineralocorticoid excess
-
White PC, Mune T, Agarwal AK. 11β-hydroxysteroid dehydrogenase and the syndrome of apparent mineralocorticoid excess. Endo Rev 1997; 18: 135-156.
-
(1997)
Endo Rev
, vol.18
, pp. 135-156
-
-
White, P.C.1
Mune, T.2
Agarwal, A.K.3
-
63
-
-
0029049742
-
Liddle's syndrome, an unrecognised entity: A report of four cases including the first report in black individuals
-
Gadallah MF, Abreo K, Work J. Liddle's syndrome, an unrecognised entity: a report of four cases including the first report in black individuals. Am J Kid Dis 1995; 25: 829-835.
-
(1995)
Am J Kid Dis
, vol.25
, pp. 829-835
-
-
Gadallah, M.F.1
Abreo, K.2
Work, J.3
-
64
-
-
0028900410
-
Glucocorticoid-remediable aldosteronism (GRA): Diagnosis, variability of phenotype and regulation of potassium homeostasis
-
Dluhy RG, Lifton RP. Glucocorticoid-remediable aldosteronism (GRA): Diagnosis, variability of phenotype and regulation of potassium homeostasis. Steroids 1995; 60: 48-51.
-
(1995)
Steroids
, vol.60
, pp. 48-51
-
-
Dluhy, R.G.1
Lifton, R.P.2
-
65
-
-
0029081279
-
Heterogenous hypertension
-
Gordon RD. Heterogenous hypertension. Nat Genet 1995; 11: 6-9.
-
(1995)
Nat Genet
, vol.11
, pp. 6-9
-
-
Gordon, R.D.1
-
66
-
-
0027320739
-
Deficient inactivation of cortisol by 11β-hydroxysteroid dehydrogenase in essential hypertension
-
Walker BR et al. Deficient inactivation of cortisol by 11β-hydroxysteroid dehydrogenase in essential hypertension. Clin Endocrinol 1993; 39: 221-227.
-
(1993)
Clin Endocrinol
, vol.39
, pp. 221-227
-
-
Walker, B.R.1
-
67
-
-
0028967443
-
Evidence of coexisting changes in 11β-hydroxysteroid dehydrogenase and 5β-reductase activity in patients with untreated essential hypertension
-
Soro A et al. Evidence of coexisting changes in 11β-hydroxysteroid dehydrogenase and 5β-reductase activity in patients with untreated essential hypertension. Hypertension 1995; 25: 67-70.
-
(1995)
Hypertension
, vol.25
, pp. 67-70
-
-
Soro, A.1
-
68
-
-
0021915854
-
Partial deficiency of adrenal 11-hydroxylase. A possible cause of primary hypertension
-
DeSimone G et al. Partial deficiency of adrenal 11-hydroxylase. A possible cause of primary hypertension. Hypertension 1985; 7: 204-210.
-
(1985)
Hypertension
, vol.7
, pp. 204-210
-
-
DeSimone, G.1
-
69
-
-
0015931464
-
Haemodynamic characteristics of primary aldosteronism
-
Tarazi RC et al. Haemodynamic characteristics of primary aldosteronism. N Engl J Med 1973; 289: 1330-1335.
-
(1973)
N Engl J Med
, vol.289
, pp. 1330-1335
-
-
Tarazi, R.C.1
-
70
-
-
0027071656
-
Central hypertensinogenic effects of glycyrrhizic acid and carbenoxolone
-
Gomez-Sanchez EP, Gomez-Sanchez CE. Central hypertensinogenic effects of glycyrrhizic acid and carbenoxolone. Am J Physiol 1992; 263: E1125-E1130.
-
(1992)
Am J Physiol
, vol.263
-
-
Gomez-Sanchez, E.P.1
Gomez-Sanchez, C.E.2
-
71
-
-
0026777230
-
Glucocorticoids and blood pressure: A role for the cortisol/cortisone shuttle in the control of vascular tone in man
-
Walker BR, Connacher AA, Webb DJ, Edwards CRW. Glucocorticoids and blood pressure: a role for the cortisol/cortisone shuttle in the control of vascular tone in man. Clin Sci 1992; 83: 171-178.
-
(1992)
Clin Sci
, vol.83
, pp. 171-178
-
-
Walker, B.R.1
Connacher, A.A.2
Webb, D.J.3
Edwards, C.R.W.4
-
72
-
-
0028173835
-
Colocalization of 11β-hydroxysteroid dehydrogenase and mineralocorticoid receptors in cultured vascular smooth muscle cells
-
Kernel L. Colocalization of 11β-hydroxysteroid dehydrogenase and mineralocorticoid receptors in cultured vascular smooth muscle cells. Am J Hypertens 1994; 7: 100-103.
-
(1994)
Am J Hypertens
, vol.7
, pp. 100-103
-
-
Kernel, L.1
-
73
-
-
0027530474
-
Dysfunction of placental glucocorticoid barrier: Link between fetal environment and adult hypertension?
-
Edwards CRW, Benediktsson R, Lindsay RS, Seckl JR. Dysfunction of placental glucocorticoid barrier: link between fetal environment and adult hypertension? Lancet 1993; 341: 355-357.
-
(1993)
Lancet
, vol.341
, pp. 355-357
-
-
Edwards, C.R.W.1
Benediktsson, R.2
Lindsay, R.S.3
Seckl, J.R.4
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