-
1
-
-
0000278245
-
Unusual steroid excretion in a child with low-renin hypertension
-
Werder E, Zachmann M, Völlmin JA, Veyrat R, Prader A. Unusual steroid excretion in a child with low-renin hypertension. Res Steroid 1975:385-95
-
(1975)
Res Steroid
, pp. 385-395
-
-
Werder, E.1
Zachmann, M.2
Völlmin, J.A.3
Veyrat, R.4
Prader, A.5
-
2
-
-
0017711792
-
Evidence for an unidentified steroid in a child with apparent mineralocorticoid hypertension
-
New MI, Levine LS, Biglieri EG, Pareira J, Ulick S. Evidence for an unidentified steroid in a child with apparent mineralocorticoid hypertension. J Clin Endocrinol Metab 1977;44:924-33
-
(1977)
J Clin Endocrinol Metab
, vol.44
, pp. 924-933
-
-
New, M.I.1
Levine, L.S.2
Biglieri, E.G.3
Pareira, J.4
Ulick, S.5
-
3
-
-
0018598286
-
A syndrome of apparent mineralocorticoid excess associated with defects in the peripheral metabolism of cortisol
-
Ulick S, Levine LS, Gunczler P, Zanconato G, Ramirez LC, Rauh W, et al. A syndrome of apparent mineralocorticoid excess associated with defects in the peripheral metabolism of cortisol. J Clin Endocrinol Metab 1979;49:757-64
-
(1979)
J Clin Endocrinol Metab
, vol.49
, pp. 757-764
-
-
Ulick, S.1
Levine, L.S.2
Gunczler, P.3
Zanconato, G.4
Ramirez, L.C.5
Rauh, W.6
-
4
-
-
0020321773
-
Partial characterization of unusual polar steroids in the urine of a child with low renin hypertension
-
Bournot M, Pitoizet N, Zachmann M, Maume BF. Partial characterization of unusual polar steroids in the urine of a child with low renin hypertension. J Steroid Biochem 1982;16:467-77
-
(1982)
J Steroid Biochem
, vol.16
, pp. 467-477
-
-
Bournot, M.1
Pitoizet, N.2
Zachmann, M.3
Maume, B.F.4
-
5
-
-
0020658534
-
Metabolic and blood pressure responses to hydrocortisone in the syndrome of apparent mineralocorticoid excess
-
Oberfield SE, Levine LS, Carey RM, Greig F, Ulick S, New MI. Metabolic and blood pressure responses to hydrocortisone in the syndrome of apparent mineralocorticoid excess. J Clin Endocrinol Metab 1983;56:332-9
-
(1983)
J Clin Endocrinol Metab
, vol.56
, pp. 332-339
-
-
Oberfield, S.E.1
Levine, L.S.2
Carey, R.M.3
Greig, F.4
Ulick, S.5
New, M.I.6
-
6
-
-
0023221667
-
Cloning of human mineralocorticoid receptor complementary DNA: Structural and functional kinship with the glucocorticoid receptor
-
Arriza JL, Weinberger C, Cerelli G, Glaser TM, Handelin BL, Housman DE, et al. Cloning of human mineralocorticoid receptor complementary DNA: structural and functional kinship with the glucocorticoid receptor. Science 1987;237:268-75
-
(1987)
Science
, vol.237
, pp. 268-275
-
-
Arriza, J.L.1
Weinberger, C.2
Cerelli, G.3
Glaser, T.M.4
Handelin, B.L.5
Housman, D.E.6
-
7
-
-
0023761690
-
Localisation of 11β-hydroxysteroid dehydrogenase - Tissue specific protector of the mineralocorticoid receptor
-
Edwards CRW, Stewart PM, Burt D, Brett L, McIntyre MA, Sutanto WS, et al. Localisation of 11β-hydroxysteroid dehydrogenase - tissue specific protector of the mineralocorticoid receptor. Lancet 1988;ii:986-9
-
(1988)
Lancet
, vol.2
, pp. 986-989
-
-
Edwards, C.R.W.1
Stewart, P.M.2
Burt, D.3
Brett, L.4
McIntyre, M.A.5
Sutanto, W.S.6
-
8
-
-
85047677780
-
Fatal, low renin hypertension associated with a disturbance of cortisol metabolism
-
Honour JW, Dillon MJ, Levin M, Shah V. Fatal, low renin hypertension associated with a disturbance of cortisol metabolism. Arch Dis Child 1983;58:1018-20
-
(1983)
Arch Dis Child
, vol.58
, pp. 1018-1020
-
-
Honour, J.W.1
Dillon, M.J.2
Levin, M.3
Shah, V.4
-
9
-
-
0024545521
-
A new form of the syndrome of apparent mineralocorticoid excess
-
Ulick S, Chan CK, Rao KN, Edassery J, Mantero F. A new form of the syndrome of apparent mineralocorticoid excess. J Steroid Biochem 1989;32:209-12
-
(1989)
J Steroid Biochem
, vol.32
, pp. 209-212
-
-
Ulick, S.1
Chan, C.K.2
Rao, K.N.3
Edassery, J.4
Mantero, F.5
-
10
-
-
0026585716
-
Defective ring a reduction of cortisol as the major metabolic error in the syndrome of apparent mineralocorticoid excess
-
Ulick S, Tedde R, Wang JZ. Defective ring A reduction of cortisol as the major metabolic error in the syndrome of apparent mineralocorticoid excess. J Clin Endocrinol Metab 1992;74:593-9
-
(1992)
J Clin Endocrinol Metab
, vol.74
, pp. 593-599
-
-
Ulick, S.1
Tedde, R.2
Wang, J.Z.3
-
11
-
-
0021883201
-
Congenital 11β-hydroxysteroid dehydrogenase deficiency associated with juvenile hypertension: Corticosteroid metabolite profiles of four patients and their families
-
Shackleton CHL, Rodriguez J, Arteaga E, Lopez JM, Winter JSD. Congenital 11β-hydroxysteroid dehydrogenase deficiency associated with juvenile hypertension: corticosteroid metabolite profiles of four patients and their families. J Clin Endocrinol Metab 1985;22:701-12
-
(1985)
J Clin Endocrinol Metab
, vol.22
, pp. 701-712
-
-
Shackleton, C.H.L.1
Rodriguez, J.2
Arteaga, E.3
Lopez, J.M.4
Winter, J.S.D.5
-
12
-
-
2542624590
-
Renal mineralocorticoid receptors and hippocampal corticosterone-binding species have identical intrinsic steroid specificity
-
Krozowski ZS, Funder JW. Renal mineralocorticoid receptors and hippocampal corticosterone-binding species have identical intrinsic steroid specificity. Proc Natl Acad Sci USA 1983;80:6056-60
-
(1983)
Proc Natl Acad Sci USA
, vol.80
, pp. 6056-6060
-
-
Krozowski, Z.S.1
Funder, J.W.2
-
13
-
-
0023743171
-
Mineralocorticoid action: Target tissue specificity is enzyme, not receptor, mediated
-
Funder JW, Pearce PT, Smith R, Smith AI. Mineralocorticoid action: target tissue specificity is enzyme, not receptor, mediated. Science 1988;242:583-5
-
(1988)
Science
, vol.242
, pp. 583-585
-
-
Funder, J.W.1
Pearce, P.T.2
Smith, R.3
Smith, A.I.4
-
14
-
-
0023242981
-
Mineralocorticoid activity of liquorice: 11-beta-hydroxysteroid dehydrogenase deficiency comes of age
-
Stewart PM, Wallace AM, Valentino R, Burt D, Shackleton CHL, Edwards CRW. Mineralocorticoid activity of liquorice: 11-beta-hydroxysteroid dehydrogenase deficiency comes of age. Lancet 1987;ii:821-4
-
(1987)
Lancet
, vol.2
, pp. 821-824
-
-
Stewart, P.M.1
Wallace, A.M.2
Valentino, R.3
Burt, D.4
Shackleton, C.H.L.5
Edwards, C.R.W.6
-
15
-
-
0027444885
-
Defects in the HSD11 gene encoding 11β-hydroxysteroid dehydrogenase are not found in patients with apparent mineralocorticoid excess or 11-oxoreductase deficiency
-
Nikkilä H, Tannin GM, New MI, Taylor NF, Kalaitzoglou G, Monder C, et al. Defects in the HSD11 gene encoding 11β-hydroxysteroid dehydrogenase are not found in patients with apparent mineralocorticoid excess or 11-oxoreductase deficiency. J Clin Endocrinol Melab 1993;77:687-91
-
(1993)
J Clin Endocrinol Melab
, vol.77
, pp. 687-691
-
-
Nikkilä, H.1
Tannin, G.M.2
New, M.I.3
Taylor, N.F.4
Kalaitzoglou, G.5
Monder, C.6
-
16
-
-
0023002861
-
Spironolactone-reversible rickets associated with 11β-hydroxysteroid dehydrogenase deficiency syndrome
-
Batista MC, Mendonca BB, Kater CE, Arnold IJP, Rocha A, Nicolau W, et al. Spironolactone-reversible rickets associated with 11β-hydroxysteroid dehydrogenase deficiency syndrome. J Pediatr 1986;109:989-93
-
(1986)
J Pediatr
, vol.109
, pp. 989-993
-
-
Batista, M.C.1
Mendonca, B.B.2
Kater, C.E.3
Arnold, I.J.P.4
Rocha, A.5
Nicolau, W.6
|