-
1
-
-
85047696604
-
Polycystic ovary syndrome as a form ovarian hyperandrogenism due to dysregulation of androgen secretion
-
Ehrmann DA, Barnes RB, Rosenfield RL. Polycystic ovary syndrome as a form ovarian hyperandrogenism due to dysregulation of androgen secretion. Endocr Rev 1995; 16:322-53.
-
(1995)
Endocr Rev
, vol.16
, pp. 322-353
-
-
Ehrmann, D.A.1
Barnes, R.B.2
Rosenfield, R.L.3
-
2
-
-
0025342494
-
A pilot study for neonatal screening of congenital adrenal hyperplasia due to 21-hydroxylase and 11β-hydroxylase deficiency in campania region
-
Valentino R, Tommaselli AP, Rossi R, Lombardi G, Varrone S. A pilot study for neonatal screening of congenital adrenal hyperplasia due to 21-hydroxylase and 11β-hydroxylase deficiency in Campania region. J Endocrinol Invest 1990; 13: 221-5.
-
(1990)
J Endocrinol Invest
, vol.13
, pp. 221-225
-
-
Valentino, R.1
Tommaselli, A.P.2
Rossi, R.3
Lombardi, G.4
Varrone, S.5
-
3
-
-
0023226909
-
Congenital adrenal hyperplasia
-
White PC, New MI, Dupont BD. Congenital adrenal hyperplasia. N Engl J Med 1987;316:1519-24.
-
(1987)
N Engl J Med
, vol.316
, pp. 1519-1524
-
-
White, P.C.1
-
4
-
-
0028154269
-
Genetics, diagnosis, and management of 21-hydroxylase deficiency
-
Miller WL. Genetics, diagnosis, and management of 21-hydroxylase deficiency. J Clin Endocrinol Metab 1994;78:241-6.
-
(1994)
J Clin Endocrinol Metab
, vol.78
, pp. 241-246
-
-
Miller, W.L.1
-
5
-
-
0028167769
-
Disorders of steroid 11β-hydroxylase isozymes
-
White PC, Curnow KM, Pascoe L. Disorders of steroid 11β-hydroxylase isozymes. Endocr Rev 1994; 15:421-38.
-
(1994)
Endocr Rev
, vol.15
, pp. 421-438
-
-
White, P.C.1
Curnow, K.M.2
Pascoe, L.3
-
6
-
-
0020028483
-
Late-onset 21-hydroxylase deficiency mimicking idiopathic hirsutism or polycystic ovarian disease
-
Chrousos GP, Loriaux D, Mann DL, Cutler GB. Late-onset 21-hydroxylase deficiency mimicking idiopathic hirsutism or polycystic ovarian disease. Ann Intern Med 1982;96:143-8.
-
(1982)
Ann Intern Med
, vol.96
, pp. 143-148
-
-
Chrousos, G.P.1
Loriaux, D.2
Mann, D.L.3
Cutler, G.B.4
-
7
-
-
0025066551
-
ACTH stimulation tests and plasma dehydroepiandrosterone sulfate levels in women with hirsutism
-
Siegel SF, Finegold DN, Lanes R, Lee PA. ACTH stimulation tests and plasma dehydroepiandrosterone sulfate levels in women with hirsutism. N Engl J Med 1990;323:849-54.
-
(1990)
N Engl J Med
, vol.323
, pp. 849-854
-
-
Siegel, S.F.1
Finegold, D.N.2
Lanes, R.3
Lee, P.A.4
-
8
-
-
0025175729
-
Secondary biosynthetic defects in women with lateonset congenital adrenal hyperplasia
-
Eldar-Geva T, Hurwitz A, Vecsei P, Palti Z, Milwidsky A, Rosier A. Secondary biosynthetic defects in women with lateonset congenital adrenal hyperplasia. N Engl J Med 1990; 323:855-63.
-
(1990)
N Engl J Med
, vol.323
, pp. 855-863
-
-
Eldar-Geva, T.1
Hurwitz, A.2
Vecsei, P.3
Palti, Z.4
Milwidsky, A.5
Rosier, A.6
-
9
-
-
0026764991
-
Adrenal disorders and polycystic ovary syndrome
-
Dunaif A. Adrenal disorders and polycystic ovary syndrome. Horm Res 1992;37:39-44.
-
(1992)
Horm Res
, vol.37
, pp. 39-44
-
-
Dunaif, A.1
-
10
-
-
0026664328
-
Detection of functional ovarian hyperandrogenism in women with androgen excess
-
Ehrmann DA, Rosenfield RL, Barnes RB, Brigell DF, Sheikh Z. Detection of functional ovarian hyperandrogenism in women with androgen excess. N Engl J Med 1992;327:157-62.
-
(1992)
N Engl J Med
, vol.327
, pp. 157-162
-
-
Ehrmann, D.A.1
Rosenfield, R.L.2
Barnes, R.B.3
Brigell, D.F.4
Sheikh, Z.5
-
11
-
-
0024444516
-
21-hydroxylase deficiency in female hyperandrogenism: Screening and diagnosis
-
Azziz R, Zacur HA. 21-hydroxylase deficiency in female hyperandrogenism: screening and diagnosis. J Clin Endocrinol Metab 1989;69:577-84.
-
(1989)
J Clin Endocrinol Metab
, vol.69
, pp. 577-584
-
-
Azziz, R.1
Zacur, H.A.2
-
12
-
-
0021915854
-
Partial deficiency of adrenal 11β-hydroxylase: A possible cause of primary hypertension
-
De Simone G, Tommaselli AP, Rossi R, Valentino R, Lauria R, Scopacasa F, et al. Partial deficiency of adrenal 11β-hydroxylase: a possible cause of primary hypertension. Hypertension 1985;7:204-10.
-
(1985)
Hypertension
, vol.7
, pp. 204-210
-
-
De Simone, G.1
Tommaselli, A.P.2
Rossi, R.3
Valentino, R.4
Lauria, R.5
Scopacasa, F.6
-
13
-
-
12644305063
-
Clinical assessment of body hair growth in women
-
Ferriman D, Galloway JD. Clinical assessment of body hair growth in women. J Clin Endocrinol Metab 1961;21:1440-7.
-
(1961)
J Clin Endocrinol Metab
, vol.21
, pp. 1440-1447
-
-
Ferriman, D.1
Galloway, J.D.2
-
14
-
-
0020556434
-
Genotyping steroid 21-hydroxylase deficiency: Hormonal reference data
-
New MI, Lorenzen F, Lener AJ, Kohn B, OberfieldSE, Pollack MS, et al. Genotyping steroid 21-hydroxylase deficiency: hormonal reference data. J Clin Endocrinol Metabol 1983; 57: 320-5.
-
(1983)
J Clin Endocrinol Metabol
, vol.57
, pp. 320-325
-
-
New, M.I.1
Lorenzen, F.2
Lener, A.J.3
Kohn, B.4
Pollack, M.S.5
-
15
-
-
0025300180
-
Prevalence of non-classical steroid 21-hydroxylase deficiency based on a morning salivary 17-hydroxyprogesterone screening test: A small sample study
-
Zerah M, Ueshiba H, Wood E, Speiser PW, Crawford C, McDonald T, et al. Prevalence of non-classical steroid 21-hydroxylase deficiency based on a morning salivary 17-hydroxyprogesterone screening test: a small sample study. J Clin Endocrinol Metab 1990;70:1662-7.
-
(1990)
J Clin Endocrinol Metab
, vol.70
, pp. 1662-1667
-
-
Zerah, M.1
Ueshiba, H.2
Wood, E.3
Speiser, P.W.4
Crawford, C.5
McDonald, T.6
-
16
-
-
0025195368
-
Dysregulation of cytochrome P450cl7α as the cause of polycystic ovarian syndrome
-
Rosenfield RL, Barnes RB, Cara JF, Lucky AW. Dysregulation of cytochrome P450cl7α as the cause of polycystic ovarian syndrome. Fertil Steril 1990;53:785-91.
-
(1990)
Fertil Steril
, vol.53
, pp. 785-791
-
-
Rosenfield, R.L.1
Barnes, R.B.2
Cara, J.F.3
Lucky, A.W.4
-
17
-
-
0027412635
-
Ovarian steroidogenic responses to gonadotropin-releasing hormone agonist testing with nafarelin in hirsute women with adrenal responses to adrenocorticotropin suggestive of 3β-hydroxydelta5-steroid dehydrogenase deficiency
-
Barnes RB, Ehrmann DA, Brigell DF, Rosenfield RL. Ovarian steroidogenic responses to gonadotropin-releasing hormone agonist testing with nafarelin in hirsute women with adrenal responses to adrenocorticotropin suggestive of 3β-hydroxydelta5-steroid dehydrogenase deficiency. J Clin Endocrinol Metab 1993; 76:450-5.
-
(1993)
J Clin Endocrinol Metab
, vol.76
, pp. 450-455
-
-
Barnes, R.B.1
Ehrmann, D.A.2
Brigell, D.F.3
Rosenfield, R.L.4
-
18
-
-
0019736397
-
Genetic and hormonal characterization of cryptic 21-hydroxylase deficiency
-
Levine LS, Dupont BO, Lorenzen F, Pang S, Pollack M, Ober-field SE, et al. Genetic and hormonal characterization of cryptic 21-hydroxylase deficiency. J Clin Endocrinol Metab 1981;54:1193-8.
-
(1981)
J Clin Endocrinol Metab
, vol.54
, pp. 1193-1198
-
-
Levine, L.S.1
Dupont, B.O.2
Lorenzen, F.3
Pang, S.4
Pollack, M.5
Ober-Field, S.E.6
-
19
-
-
0024787154
-
Congenital adrenal hyperplasia due to combined 21-and 11β-hydroxylase deficiency
-
Penny R, Vecsei P. Congenital adrenal hyperplasia due to combined 21-and 11β-hydroxylase deficiency. J Endocrinol Invest 1989; 12:723-8.
-
(1989)
J Endocrinol Invest
, vol.12
, pp. 723-728
-
-
Penny, R.1
Vecsei, P.2
-
20
-
-
0023830902
-
Zona glomerulosa function after life-long suppression in two siblings with the hypertensive virilizing form of congenital adrenal hyperplasia
-
Portales JAR, Arteaga E, Moreno JML, Biglieri EG. Zona glomerulosa function after life-long suppression in two siblings with the hypertensive virilizing form of congenital adrenal hyperplasia. J Clin Endocrinol Metab 1988;66:349-54.
-
(1988)
J Clin Endocrinol Metab
, vol.66
, pp. 349-354
-
-
Portales, J.A.R.1
Arteaga, E.2
Moreno, J.M.L.3
Biglieri, E.G.4
-
21
-
-
0024521545
-
Increased plasma 21-deoxycorticosterone (21-DB) levels in late-onset adrenal 21-hydroxylase deficiency suggest a mild defect of the mineralocorticoid pathway
-
Fiet J, Gueux B, Raux-Demay MC, Kuttenn F, Vexiau P, Brerault JL, et al. Increased plasma 21-deoxycorticosterone (21-DB) levels in late-onset adrenal 21-hydroxylase deficiency suggest a mild defect of the mineralocorticoid pathway. J Clin Endocrinol Metab 1989;68:542-7.
-
(1989)
J Clin Endocrinol Metab
, vol.68
, pp. 542-547
-
-
Fiet, J.1
Gueux, B.2
Raux-Demay, M.C.3
Kuttenn, F.4
Vexiau, P.5
Brerault, J.L.6
-
22
-
-
0026096930
-
11β-hydroxylase deficiency in hyperandrogenism
-
Azziz R, Boots LR, Parker CR Jr, Bradley E Jr, Zacur HA. 11β-hydroxylase deficiency in hyperandrogenism. Fertil Steril 1991;55:733-41.
-
(1991)
Fertil Steril
, vol.55
, pp. 733-741
-
-
Azziz, R.1
Boots, L.R.2
Parker C.R., Jr.3
Bradley E., Jr.4
Zacur, H.A.5
-
23
-
-
0021993387
-
Late-onset adrenal steroid 3β-hydroxysteroid dehydrogenase deficiency. I. A cause of hirsutism in pubertal and postpubertal women
-
Pang S, Lerner AJ, Stoner E, Levine LS, Oberfield SE, Engel I, et al. Late-onset adrenal steroid 3β-hydroxysteroid dehydrogenase deficiency. I. A cause of hirsutism in pubertal and postpubertal women. J Clin Endocrinol Metab 1985;60:428-39.
-
(1985)
J Clin Endocrinol Metab
, vol.60
, pp. 428-439
-
-
Pang, S.1
Lerner, A.J.2
Stoner, E.3
Levine, L.S.4
Oberfield, S.E.5
Engel, I.6
-
24
-
-
84995870589
-
Plasma 3β-hydroxy-delta5-steroids in patients with congential adrenal hyperplasia due to 21-hydroxylase deficiency
-
Young J, Couzinet B, Pholsena M, Nahoul K, Labrie F, Schaison G. Plasma 3β-hydroxy-delta5-steroids in patients with congential adrenal hyperplasia due to 21-hydroxylase deficiency. J Clin Endocrinol Metab 1994:78:299-304.
-
(1994)
J Clin Endocrinol Metab
, vol.78
, pp. 299-304
-
-
Young, J.1
Couzinet, B.2
Pholsena, M.3
Nahoul, K.4
Labrie, F.5
Schaison, G.6
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