-
1
-
-
0000697658
-
The adrenal cortex, in Felig P, Baxter J, Frohman L (eds)
-
New York, McGraw Hill
-
Miller WL, Tyrrell JB: The adrenal cortex, in Felig P, Baxter J, Frohman L (eds): Endocrinology and Metabolism. New York, McGraw Hill, 1995, pp 555-717.
-
(1995)
Endocrinology and Metabolism.
, pp. 555-717
-
-
Miller, W.L.1
Tyrrell, J.B.2
-
2
-
-
0019332509
-
Studies on the steroid hydroxylation system in adrenal cortex microsomes: Purification and characterization of cytochrome P450 specific for steroid 21 hydroxylation
-
Kominami S, Ochi H, Kobayashi Y, et al: Studies on the steroid hydroxylation system in adrenal cortex microsomes: Purification and characterization of cytochrome P450 specific for steroid 21 hydroxylation. JBiol Chem 255:3386-3394, 1980.
-
(1980)
JBiol Chem
, vol.255
, pp. 3386-3394
-
-
Kominami, S.1
Ochi, H.2
Kobayashi, Y.3
-
3
-
-
0024460383
-
Extra-adrenal steroid 21-hydroxylation is not mediated by P450c21
-
Mellon SH, Miller WL: Extra-adrenal steroid 21-hydroxylation is not mediated by P450c21. J Clin Invest 84:1497-1502, 1989.
-
(1989)
J Clin Invest
, vol.84
, pp. 1497-1502
-
-
Mellon, S.H.1
Miller, W.L.2
-
4
-
-
0020188787
-
Extra-adrenal formation of a mineralocorticoid: Deoxycorticosterone and deoxycorticosterone sulfate biosynthesis and metabolism
-
Casey ML, MacDonald PC: Extra-adrenal formation of a mineralocorticoid: Deoxycorticosterone and deoxycorticosterone sulfate biosynthesis and metabolism. Endocr Rev 3:396-403, 1982.
-
(1982)
Endocr Rev
, vol.3
, pp. 396-403
-
-
Casey, M.L.1
MacDonald, P.C.2
-
5
-
-
0026074413
-
Aldosterone synthesis in patients with salt-wasting congenital adrenal hyperplasia (21hydroxylase deficiency) and complete absence of adrenal 21hydroxylase (P450c21)
-
Speiser PW, Agdere L, Veshiba H, et al: Aldosterone synthesis in patients with salt-wasting congenital adrenal hyperplasia (21hydroxylase deficiency) and complete absence of adrenal 21hydroxylase (P450c21). N Engl J Med 321:145-149, 1991.
-
(1991)
N Engl J Med
, vol.321
, pp. 145-149
-
-
Speiser, P.W.1
Agdere, L.2
Veshiba, H.3
-
6
-
-
0010430717
-
Mapping of steroid 21hydroxylase genes to complement component C4 genes in HLA, the major histocompatibility locus in man
-
Carroll MC, Campbell RD, Porter RR: Mapping of steroid 21hydroxylase genes to complement component C4 genes in HLA, the major histocompatibility locus in man. Proc Natl Acad Sei USA 82:521-525, 1985.
-
(1985)
Proc Natl Acad Sei USA
, vol.82
, pp. 521-525
-
-
Carroll, M.C.1
Campbell, R.D.2
Porter, R.R.3
-
7
-
-
0021914293
-
Two genes encoding steroid 21-hydroxylase are located near the genes encoding the fourth component of complement in man
-
White PC, Grossberger D, Onufer B], et al: Two genes encoding steroid 21-hydroxylase are located near the genes encoding the fourth component of complement in man. Proc Natl Acad Sei USA 82:10891093, 1985.
-
(1985)
Proc Natl Acad Sei USA
, vol.82
, pp. 10891093
-
-
White, P.C.1
Grossberger, D.2
Onufer, B.3
-
8
-
-
0027231385
-
Tenascin-X. A novel extracellular matrix protein encoded by the human XB gene overlapping P450c2lB
-
Bristow J, Tee MK, Gitelman SE, et al: Tenascin-X. A novel extracellular matrix protein encoded by the human XB gene overlapping P450c2lB. J Cell Biol 122:265-278, 1993.
-
(1993)
J Cell Biol
, vol.122
, pp. 265-278
-
-
Bristow, J.1
Tee, M.K.2
Gitelman, S.E.3
-
9
-
-
0030843025
-
Tenascin-X deficiency is associated with Ehlers-Danlos syndrome
-
Burch GH, Gong Y, Liu W, et al: Tenascin-X deficiency is associated with Ehlers-Danlos syndrome. Nat Genet 17:104-108, 1997.
-
(1997)
Nat Genet
, vol.17
, pp. 104-108
-
-
Burch, G.H.1
Gong, Y.2
Liu, W.3
-
10
-
-
0042901202
-
Complete nucleotide sequence of two steroid 21-hydroxylase genes tandemly arranged in human chromosome: A pseudogene and genuine gene
-
Higashi Y, Yoshioka H, Yamane M, et al: Complete nucleotide sequence of two steroid 21-hydroxylase genes tandemly arranged in human chromosome: A pseudogene and genuine gene. Proc Natl Acad Sei USA 83:2841-2845, 1986.
-
(1986)
Proc Natl Acad Sei USA
, vol.83
, pp. 2841-2845
-
-
Higashi, Y.1
Yoshioka, H.2
Yamane, M.3
-
11
-
-
0007996186
-
Structure of the human steroid 21-hydroxylase genes
-
White PC, New MI, Dupont B: Structure of the human steroid 21-hydroxylase genes. Proc Natl Acad Sei USA 83:5111-5115, 1986.
-
(1986)
Proc Natl Acad Sei USA
, vol.83
, pp. 5111-5115
-
-
White, P.C.1
New, M.I.2
Dupont, B.3
-
12
-
-
0023354308
-
Molecular characterization of the HLA-linked steroid 21-hydroxylase B gene from an individual with congenital adrenal hyperplasia
-
Rodrigues NR, Dunham I, Yu CY, et al: Molecular characterization of the HLA-linked steroid 21-hydroxylase B gene from an individual with congenital adrenal hyperplasia. EMBO J 6:1653-1661, 1987.
-
(1987)
EMBO J
, vol.6
, pp. 1653-1661
-
-
Rodrigues, N.R.1
Dunham, I.2
Yu, C.Y.3
-
13
-
-
0027319656
-
Abundant adrenal-specific transcription of the human P450c21A "pseudogene."
-
Bristow J, Gitelman SE, Tee MK, et al: Abundant adrenal-specific transcription of the human P450c21A "pseudogene." J Biol Chem 268:12919-12924, 1993.
-
(1993)
J Biol Chem
, vol.268
, pp. 12919-12924
-
-
Bristow, J.1
Gitelman, S.E.2
Tee, M.K.3
-
14
-
-
0029101053
-
Difference in transcriptional activity of two homologous CYP21A genes
-
Chang SF, Chung B: Difference in transcriptional activity of two homologous CYP21A genes. Mol Endocrinol 9:1330-1336, 1995.
-
(1995)
Mol Endocrinol
, vol.9
, pp. 1330-1336
-
-
Chang, S.F.1
Chung, B.2
-
15
-
-
33749285881
-
Normal and CAH mutant 21-hydroxylase promoter activities differ in an in vitro luciferase promoter assay
-
Donohoue PA, Wedell A: Normal and CAH mutant 21-hydroxylase promoter activities differ in an in vitro luciferase promoter assay. Harm Res 48:978, 1997.
-
(1997)
Harm Res
, vol.48
, pp. 978
-
-
Donohoue, P.A.1
Wedell, A.2
-
16
-
-
0007053474
-
P450XXI (steroid 21-hydroxylase) gene deletions are not found in family studies of congenital adrenal hyperplasia
-
Matteson KJ, Phillips JA III, Miller WL, et al: P450XXI (steroid 21-hydroxylase) gene deletions are not found in family studies of congenital adrenal hyperplasia. Proc Natl Acad Sei USA 84:5858-5862, 1987.
-
(1987)
Proc Natl Acad Sei USA
, vol.84
, pp. 5858-5862
-
-
Matteson, K.J.1
Phillips III, J.A.2
Miller, W.L.3
-
17
-
-
0024808985
-
Molecular genetics of 21-hydroxylase deficiency
-
Miller WL, Morel Y: Molecular genetics of 21-hydroxylase deficiency. Annu Rev Genet 23:371-393, 1989.
-
(1989)
Annu Rev Genet
, vol.23
, pp. 371-393
-
-
Miller, W.L.1
Morel, Y.2
-
18
-
-
0026641101
-
Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiency
-
Speiser PW, Dupont J, Zhu D, et al: Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiency. J Clin Invest 90:584-595, 1992.
-
(1992)
J Clin Invest
, vol.90
, pp. 584-595
-
-
Speiser, P.W.1
Dupont, J.2
Zhu, D.3
-
19
-
-
0028786666
-
Gene conversions and unequal crossovers between CYP21 (steroid 21-hydroxylase gene) and CYP21P involve different mechanisms
-
Tusie-Luna MT, White PC: Gene conversions and unequal crossovers between CYP21 (steroid 21-hydroxylase gene) and CYP21P involve different mechanisms. Proc Natl Acad Sei USA 92:10796-10800, 1995.
-
(1995)
Proc Natl Acad Sei USA
, vol.92
, pp. 10796-10800
-
-
Tusie-Luna, M.T.1
White, P.C.2
-
20
-
-
0025935967
-
Clinical and molecular genetics of congenital adrenal hyperplasia due to 21-hydroxylase deficiency
-
Morel Y, Miller WL: Clinical and molecular genetics of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Adv Hum Genet 20:1-68, 1991.
-
(1991)
Adv Hum Genet
, vol.20
, pp. 1-68
-
-
Morel, Y.1
Miller, W.L.2
-
21
-
-
0028208951
-
Mutational spectrum of the steroid 21-hydroxylase gene in Sweden: Implications for genetic diagnosis and association with disease manifestation
-
Wedell A, Thilén A, Ritzen EM, et al: Mutational spectrum of the steroid 21-hydroxylase gene in Sweden: Implications for genetic diagnosis and association with disease manifestation. J Clin Endocrinol Metab 78:1145-1152, 1994.
-
(1994)
J Clin Endocrinol Metab
, vol.78
, pp. 1145-1152
-
-
Wedell, A.1
Thilén, A.2
Ritzen, E.M.3
-
22
-
-
0029034192
-
Rapid DMA analysis by allelespecific PCR for detection of mutations in the steroid 21-hydroxylase gene
-
Wilson RC, Wei J-Q, Cheang KG, et al: Rapid DMA analysis by allelespecific PCR for detection of mutations in the steroid 21-hydroxylase gene. J Clin Endocrinol Metab 80:1635-1640, 1995.
-
(1995)
J Clin Endocrinol Metab
, vol.80
, pp. 1635-1640
-
-
Wilson, R.C.1
Wei, J.-Q.2
Cheang, K.G.3
-
23
-
-
0023623002
-
Gene conversion-like events cause steroid 21-hydroxylase deficiency in congenital adrenal hyperplasia
-
Harada F, Kimura A, Iwanaga T, et al: Gene conversion-like events cause steroid 21-hydroxylase deficiency in congenital adrenal hyperplasia. Proc Natl Acad Sei USA 84:8091-8094, 1987.
-
(1987)
Proc Natl Acad Sei USA
, vol.84
, pp. 8091-8094
-
-
Harada, F.1
Kimura, A.2
Iwanaga, T.3
-
24
-
-
0023915848
-
Evidence for frequent gene conversions in the steroid 21-hydroxylase (P-450c21) gene: Implications for steroid 21-hydroxylase deficiency
-
Higashi Y, Tanae A, Inoue H, et al: Evidence for frequent gene conversions in the steroid 21-hydroxylase (P-450c21) gene: Implications for steroid 21-hydroxylase deficiency. Am J Hum Genet 42:17-25, 1988.
-
(1988)
Am J Hum Genet
, vol.42
, pp. 17-25
-
-
Higashi, Y.1
Tanae, A.2
Inoue, H.3
-
25
-
-
0007383587
-
Mutation in the CYP21B gene (Ile-172-Asn) causes steroid 21-hydroxylase deficiency
-
Amor M, Parker KL, Globerman H, et al: Mutation in the CYP21B gene (Ile-172-Asn) causes steroid 21-hydroxylase deficiency. Proc Natl Acad Sei USA 85:1600-1604, 1988.
-
(1988)
Proc Natl Acad Sei USA
, vol.85
, pp. 1600-1604
-
-
Amor, M.1
Parker, K.L.2
Globerman, H.3
-
26
-
-
0023689994
-
Nonsense mutation causing steroid 21-hydroxylase deficiency
-
Globerman H, Amor M, Parker PL, et al: Nonsense mutation causing steroid 21-hydroxylase deficiency. J Clin Invest 82:139-144, 1988.
-
(1988)
J Clin Invest
, vol.82
, pp. 139-144
-
-
Globerman, H.1
Amor, M.2
Parker, P.L.3
-
27
-
-
0032488666
-
Cytochrome b5 augments the 17,20 lyase activity of human P450cl7 without direct electron transfer
-
Auchus RJ, Lee TC, Miller WL: Cytochrome b5 augments the 17,20 lyase activity of human P450cl7 without direct electron transfer. JBiol Chem 273:3158-3165, 1998.
-
(1998)
JBiol Chem
, vol.273
, pp. 3158-3165
-
-
Auchus, R.J.1
Lee, T.C.2
Miller, W.L.3
-
28
-
-
0023951040
-
Comparison of basal and adrenocorticotropin-stimulated plasma 21-desoxycortisol and 17hydroprogesterone values as biological markers of late-onset adrenal hyperplasia
-
Fiet J, Gueux B, Gourmelen M, et al: Comparison of basal and adrenocorticotropin-stimulated plasma 21-desoxycortisol and 17hydroprogesterone values as biological markers of late-onset adrenal hyperplasia. J Clin Endocrinol Metab 66:659-667, 1988.
-
(1988)
J Clin Endocrinol Metab
, vol.66
, pp. 659-667
-
-
Fiet, J.1
Gueux, B.2
Gourmelen, M.3
-
29
-
-
0028154269
-
Genetics, diagnosis, and management of 21-hydroxylase deficiency
-
Miller WL: Genetics, diagnosis, and management of 21-hydroxylase deficiency. J Clin Endocrinol Metab 78:241-246, 1994.
-
(1994)
J Clin Endocrinol Metab
, vol.78
, pp. 241-246
-
-
Miller, W.L.1
-
30
-
-
0023903807
-
Worldwide experience in newborn screening for classical congenital adrenal hyperplasia due to 21hydroxylase deficiency
-
Pang S, Wallace MA, Hofman L, et al: Worldwide experience in newborn screening for classical congenital adrenal hyperplasia due to 21hydroxylase deficiency. Pediatrics 81:866-874, 1988.
-
(1988)
Pediatrics
, vol.81
, pp. 866-874
-
-
Pang, S.1
Ma, W.2
Hofman, L.3
-
31
-
-
2642620230
-
Results of screening 1.9 million Texas newborns for 21-hydroxylase-deficient congenital adrenal hyperplasia
-
Therrell BL Jr, Berenbaum SA, Manter-Kapanke V, et al: Results of screening 1.9 million Texas newborns for 21-hydroxylase-deficient congenital adrenal hyperplasia. Pediatrics 101:583-590, 1998.
-
(1998)
Pediatrics
, vol.101
, pp. 583-590
-
-
Therrell Jr., B.L.1
Berenbaum, S.A.2
Manter-Kapanke, V.3
-
32
-
-
0022219639
-
High frequency of nonclassical steroid 21-hydroxylase deficiency
-
Speiser PW, Dupont B, Rubinstein P, et al: High frequency of nonclassical steroid 21-hydroxylase deficiency. Am J Hum Genet 37:650-667, 1985.
-
(1985)
Am J Hum Genet
, vol.37
, pp. 650-667
-
-
Speiser, P.W.1
Dupont, B.2
Rubinstein, P.3
-
33
-
-
0018934993
-
The attenuated form of congenital adrenal hyperplasia as an allelic form of 21-hydroxylase deficiency. 7
-
Migeon CJ, Rosenwask Z, Lee PA, et al: The attenuated form of congenital adrenal hyperplasia as an allelic form of 21-hydroxylase deficiency. 7 Clin Endocrinol Metab 51:647-649, 1980.
-
(1980)
Clin Endocrinol Metab
, vol.51
, pp. 647-649
-
-
Migeon, C.J.1
Rosenwask, Z.2
Lee, P.A.3
-
34
-
-
0020296241
-
Late-onset steroid 21hydroxylase deficiency: A variant of classical congenital adrenal hyperplasia. 7
-
Kohn B, Levine LS, Pollack MS, et al: Late-onset steroid 21hydroxylase deficiency: A variant of classical congenital adrenal hyperplasia. 7 Clin Endocrinol Metab 51:817-827, 1982.
-
(1982)
Clin Endocrinol Metab
, vol.51
, pp. 817-827
-
-
Kohn, B.1
Levine, L.S.2
Pollack, M.S.3
-
35
-
-
0020028483
-
Late-onset 21-hydroxylase deficiency mimicking idiopathic hirsutism or polycystic ovarian disease: An allelic variant of congenital virilizing adrenal hyperplasia with a milder enzymatic defect
-
Chrousos GP, Loriaux DL, Mann DL, et al: Late-onset 21-hydroxylase deficiency mimicking idiopathic hirsutism or polycystic ovarian disease: An allelic variant of congenital virilizing adrenal hyperplasia with a milder enzymatic defect. Ann Intern Med 96:143-148, 1982.
-
(1982)
Ann Intern Med
, vol.96
, pp. 143-148
-
-
Chrousos, G.P.1
Loriaux, D.L.2
Mann, D.L.3
-
36
-
-
0021264270
-
The incidence of the lateonset congenital adrenal hyperplasia due to 21-hydroxylase deficiency among hirsute women
-
Chetkowski RJ, DeFazio J, Shamonki I, et al: The incidence of the lateonset congenital adrenal hyperplasia due to 21-hydroxylase deficiency among hirsute women. J Clin Endocrinol Metab 58:595-598, 1984.
-
(1984)
J Clin Endocrinol Metab
, vol.58
, pp. 595-598
-
-
Chetkowski, R.J.1
Defazio, J.2
Shamonki, I.3
-
37
-
-
0021830172
-
Late-onset adrenal hyperplasia in hirsutism
-
Kuttenn F, Couillin P, Girard F, et al: Late-onset adrenal hyperplasia in hirsutism. N Engl J Med 313:222-231, 1985.
-
(1985)
N Engl J Med
, vol.313
, pp. 222-231
-
-
Kuttenn, F.1
Couillin, P.2
Girard, F.3
-
39
-
-
0024444516
-
21-Hydroxylase deficiency in female hyperandrogenism: Screening and diagnosis
-
Azziz R, Zacur A: 21-Hydroxylase deficiency in female hyperandrogenism: Screening and diagnosis. J Clin Endocrinol Metab 69:577-584, 1989.
-
(1989)
J Clin Endocrinol Metab
, vol.69
, pp. 577-584
-
-
Azziz, R.1
Zacur, A.2
-
40
-
-
0028899597
-
Hyperandrogenic anovulation (PCOS): A unique disorder of insulin action associated with an increased risk of non-insulindependent diabetes mellitus
-
Dunaif A: Hyperandrogenic anovulation (PCOS): A unique disorder of insulin action associated with an increased risk of non-insulindependent diabetes mellitus. AmJMed 98:33S-39S, 1995.
-
(1995)
AmJMed
, vol.98
-
-
Dunaif, A.1
-
41
-
-
0019736397
-
Genetic and hormonal characterization of the cryptic 21-hydroxylase deficiency
-
Levine LS, Dupont B, Lorenzen F, et al: Genetic and hormonal characterization of the cryptic 21-hydroxylase deficiency. J Clin Endocrinol Metab 53:1193-1198, 1981.
-
(1981)
J Clin Endocrinol Metab
, vol.53
, pp. 1193-1198
-
-
Levine, L.S.1
Dupont, B.2
Lorenzen, F.3
-
42
-
-
0020556434
-
Genotyping steroid 21hydroxylase deficiency: Hormonal reference data
-
New MI, Lorenzen F, Lerner AJ, et al: Genotyping steroid 21hydroxylase deficiency: Hormonal reference data. J Clin Endocrinol Metab 57:320-326, 1983.
-
(1983)
J Clin Endocrinol Metab
, vol.57
, pp. 320-326
-
-
New, M.I.1
Lorenzen, F.2
Lerner, A.J.3
-
43
-
-
0030928014
-
Prophylactic adrenalectomy of a three-year-old girl with congenital adrenal hyperplasia: Preand postoperative studies
-
Günther DF, Bukowski TP, Ritzen EM, et al: Prophylactic adrenalectomy of a three-year-old girl with congenital adrenal hyperplasia: Preand postoperative studies. J Clin Endocrinol Metab 82:3324-3327, 1997.
-
(1997)
J Clin Endocrinol Metab
, vol.82
, pp. 3324-3327
-
-
Günther, D.F.1
Bukowski, T.P.2
Ritzen, E.M.3
-
44
-
-
0029846160
-
A preliminary study of flutamide, testolactone, and reduced hydrocortisone dose in the treatment of congenital adrenal hyperplasia
-
Laue L, Merke DP, Jones JV, et al: A preliminary study of flutamide, testolactone, and reduced hydrocortisone dose in the treatment of congenital adrenal hyperplasia. J Clin Endocrinol Metab 81:3535-3539, 1996.
-
(1996)
J Clin Endocrinol Metab
, vol.81
, pp. 3535-3539
-
-
Laue, L.1
Merke, D.P.2
Jones, J.V.3
-
45
-
-
0002948430
-
Disorders of sexual differentiation
-
in Wilson JD, Foster D (eds): Philadelphia
-
Grumbach MM, Conte FA: Disorders of sexual differentiation, in Wilson JD, Foster D (eds): Williams' Textbook of Endocrinology. Philadelphia, 1992, pp 853-952.
-
(1992)
Williams' Textbook of Endocrinology.
, pp. 853-952
-
-
Grumbach, M.M.1
Conte, F.A.2
-
46
-
-
0023113704
-
Fertility rates in female patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
-
Mulaikal RM, Migeon CJ, Rock JA: Fertility rates in female patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. N Engl JMed 316:178-182, 1987.
-
(1987)
N Engl JMed
, vol.316
, pp. 178-182
-
-
Mulaikal, R.M.1
Migeon, C.J.2
Rock, J.A.3
-
47
-
-
0026660541
-
Sexual behavior in adolescent and adult females with congenital adrenal hyperplasia
-
Dittmann RW, Kappes ME, Kappes MH: Sexual behavior in adolescent and adult females with congenital adrenal hyperplasia. Psychoneuroendocrinology 17:153-170, 1992.
-
(1992)
Psychoneuroendocrinology
, vol.17
, pp. 153-170
-
-
Dittmann, R.W.1
Kappes, M.E.2
Kappes, M.H.3
-
48
-
-
0027466656
-
Partnership and sexuality in adult female patients with congenital adrenal hyperplasia. First results of a cross-sectional quality-of-life evaluation
-
Kuhnle U, Bollinger M, Schwarz HP, et al: Partnership and sexuality in adult female patients with congenital adrenal hyperplasia. First results of a cross-sectional quality-of-life evaluation. J Steroid Biochem Mol Biol 45:123-126, 1993.
-
(1993)
J Steroid Biochem Mol Biol
, vol.45
, pp. 123-126
-
-
Kuhnle, U.1
Bollinger, M.2
Schwarz, H.P.3
-
49
-
-
0030423478
-
Psychosexual development of women with congenital adrenal hyperplasia
-
Zucker KJ, Bradley SJ, Oliver G, et al: Psychosexual development of women with congenital adrenal hyperplasia. Harm Behav 30:300-318, 1996.
-
(1996)
Harm Behav
, vol.30
, pp. 300-318
-
-
Zucker, K.J.1
Bradley, S.J.2
Oliver, G.3
-
50
-
-
0030423655
-
Gender change from female to male in classical congenital adrenal hyperplasia
-
Meyer-Bahlburg HFL, Gruen RS, New MI, et al: Gender change from female to male in classical congenital adrenal hyperplasia. Horm Behav 30:319-332, 1996.
-
(1996)
Horm Behav
, vol.30
, pp. 319-332
-
-
Hfl, M.-B.1
Gruen, R.S.2
New, M.I.3
-
51
-
-
33749304165
-
Normal female offspring in mothers with salt-losing form of 21-hydroxylase deficiency
-
Schwitzgebel VM, Kaplan SL, Grumbach MM, et al: Normal female offspring in mothers with salt-losing form of 21-hydroxylase deficiency. Horm Res 48:33S, 1997.
-
(1997)
Horm Res
, vol.48
-
-
Schwitzgebel, V.M.1
Kaplan, S.L.2
Grumbach, M.M.3
-
52
-
-
0031046241
-
Ll-hydroxysteroid dehydrogenase and the syndrome of apparent mineralocorticoid excess
-
White PC, Mune T, Agarwal AK: ll-hydroxysteroid dehydrogenase and the syndrome of apparent mineralocorticoid excess. Endocr Rev 18:135-156, 1997.
-
(1997)
Endocr Rev
, vol.18
, pp. 135-156
-
-
White, P.C.1
Mune, T.2
Agarwal, A.K.3
-
53
-
-
0027538375
-
Prenatal diagnosis and treatment of 21hydroxylase deficiency
-
Forest MG, David M, Morel Y: Prenatal diagnosis and treatment of 21hydroxylase deficiency. J Steroid Biochem Mol Biol 45:75-82, 1993.
-
(1993)
J Steroid Biochem Mol Biol
, vol.45
, pp. 75-82
-
-
Forest, M.G.1
David, M.2
Morel, Y.3
-
54
-
-
0027936379
-
Prenatal diagnosis and management of congenital adrenal hyperplasia
-
Speiser PW, New MI: Prenatal diagnosis and management of congenital adrenal hyperplasia. Clin Perinatal 21:631-645, 1994.
-
(1994)
Clin Perinatal
, vol.21
, pp. 631-645
-
-
Speiser, P.W.1
New, M.I.2
-
55
-
-
0029006995
-
Prenatal treatment and diagnosis of congenital adrenal hyperplasia owing to 21-hydroxylase deficiency
-
Mercado AB, Wilson RC, Cheng KG, et al: Prenatal treatment and diagnosis of congenital adrenal hyperplasia owing to 21-hydroxylase deficiency. J Clin Endocrinol Metab 80:2014-2020, 1995.
-
(1995)
J Clin Endocrinol Metab
, vol.80
, pp. 2014-2020
-
-
Mercado, A.B.1
Wilson, R.C.2
Cheng, K.G.3
-
56
-
-
0030961591
-
How safe is long-term prenatal glucocorticoid treatment?
-
Seckl JR, Miller WL: How safe is long-term prenatal glucocorticoid treatment? JAMA 277:1077-1079, 1997.
-
(1997)
JAMA
, vol.277
, pp. 1077-1079
-
-
Seckl, J.R.1
Miller, W.L.2
-
57
-
-
0032171282
-
Prenatal treatment of congenital adrenal hyperplasia-a promising experimental therapy of unproven safety
-
Miller WL: Prenatal treatment of congenital adrenal hyperplasia-a promising experimental therapy of unproven safety. Trends Endocrinol Metab 9:290-293, 1998.
-
(1998)
Trends Endocrinol Metab
, vol.9
, pp. 290-293
-
-
Miller, W.L.1
-
58
-
-
0027322946
-
Molecular basis of congenital adrenal hyperplasia due to 3-hydroxysteroid dehydrogenase deficiency
-
Simard J, Rhéaume E, Sanchez R, et al: Molecular basis of congenital adrenal hyperplasia due to 3-hydroxysteroid dehydrogenase deficiency. Mol Endocrinol 7:716-728, 1993.
-
(1993)
Mol Endocrinol
, vol.7
, pp. 716-728
-
-
Simard, J.1
Rhéaume, E.2
Sanchez, R.3
-
59
-
-
0021875466
-
Pitfalls of prenatal diagnosis of 21hydroxylase deficiency congenital adrenal hyperplasia
-
Pang S, Pollack MS, Loo M, et al: Pitfalls of prenatal diagnosis of 21hydroxylase deficiency congenital adrenal hyperplasia. J Clin Endocrinol Metab 61:89, 1985.
-
(1985)
J Clin Endocrinol Metab
, vol.61
, pp. 89
-
-
Pang, S.1
Pollack, M.S.2
Loo, M.3
-
60
-
-
0027499263
-
3-hydroxysteroid dehydrogenase deficiency in hyperandrogenism
-
Azziz R, Bradley ELJ, Potter HD, et al: 3-hydroxysteroid dehydrogenase deficiency in hyperandrogenism. Am J Obstet Gynecol 168:889895, 1993.
-
(1993)
Am J Obstet Gynecol
, vol.168
, pp. 889895
-
-
Azziz, R.1
Elj, B.2
Potter, H.D.3
-
61
-
-
0029033431
-
Absence of molecular defect in the Type II 3-hydroxysteroid dehydrogenase (3-HSD) gene in premature pubarche children and hirsute female patients with moderately decreased adrenal 3-HSD activity
-
Chang YT, Zhang L, Alkaddour HS, et al: Absence of molecular defect in the Type II 3-hydroxysteroid dehydrogenase (3-HSD) gene in premature pubarche children and hirsute female patients with moderately decreased adrenal 3-HSD activity. Pediatr Res 37:820-824, 1995.
-
(1995)
Pediatr Res
, vol.37
, pp. 820-824
-
-
Chang, Y.T.1
Zhang, L.2
Alkaddour, H.S.3
-
62
-
-
0029798423
-
Studies of 3hydroxysteroid dehydrogenase genes in infants and children manifesting premature pubarche and increased adrenocorticotropinstimulated A5-steroid levels
-
Sakkal-Alkaddour H, Zhang L, Yang X, et al: Studies of 3hydroxysteroid dehydrogenase genes in infants and children manifesting premature pubarche and increased adrenocorticotropinstimulated A5-steroid levels. J Clin Endocrinol Metab 81:3961-3965, 1996.
-
(1996)
J Clin Endocrinol Metab
, vol.81
, pp. 3961-3965
-
-
Sakkal-Alkaddour, H.1
Zhang, L.2
Yang, X.3
-
63
-
-
0031969057
-
The molecular and clinical spectrum of 3-hydroxysteroid dehydrogenase deficiency disorder
-
Pang S: The molecular and clinical spectrum of 3-hydroxysteroid dehydrogenase deficiency disorder. Trends Endocrinol Metab 9:82-86, 1998.
-
(1998)
Trends Endocrinol Metab
, vol.9
, pp. 82-86
-
-
Pang, S.1
|