-
1
-
-
78049419925
-
Multiple courses of antenatal corticosteroids for preterm birth study: 2-year outcomes
-
Asztalos, E. V., Murphy, K. E., Hannah, M. E., Willan, A. R., Matthews, S. G., Ohlsson, A., et al. (2010). Multiple courses of antenatal corticosteroids for preterm birth study: 2-year outcomes. Pediatrics, 126, e1045-e1055.
-
(2010)
Pediatrics
, vol.126
-
-
Asztalos, E.V.1
Murphy, K.E.2
Hannah, M.E.3
Willan, A.R.4
Matthews, S.G.5
Ohlsson, A.6
-
2
-
-
0024469193
-
Weight in infancy and death from ischaemic heart disease
-
Barker, D. J. P.,Winter, P. D., Osmond, C., Margetts, B., & Simmonds, S. J. (1989). Weight in infancy and death from ischaemic heart disease. Lancet, 2, 577-580.
-
(1989)
Lancet
, vol.2
, pp. 577-580
-
-
Barker, D.J.P.1
Winter, P.D.2
Osmond, C.3
Margetts, B.4
Simmonds, S.J.5
-
3
-
-
0025297450
-
Fetal and placental size and risk of hypertension in adult life
-
Barker, D. J. P., Bull, A. R., Osmond, C., & Simmonds, S. J. (1990). Fetal and placental size and risk of hypertension in adult life. British Medical Journal, 301, 259-262.
-
(1990)
British Medical Journal
, vol.301
, pp. 259-262
-
-
Barker, D.J.P.1
Bull, A.R.2
Osmond, C.3
Simmonds, S.J.4
-
4
-
-
0027529974
-
Type 2 (non-insulin-dependent) diabetes mellitus, hypertension and hyperlipidaemia (syndrome X): Relation to reduced fetal growth
-
Barker, D. J., Hales, C. N., Fall, C. H., Osmond, C., Phipps, K., & Clark, P. M. (1993). Type 2 (non-insulin-dependent) diabetes mellitus, hypertension and hyperlipidaemia (syndrome X): relation to reduced fetal growth. Diabetologia, 36, 62-67.
-
(1993)
Diabetologia
, vol.36
, pp. 62-67
-
-
Barker, D.J.1
Hales, C.N.2
Fall, C.H.3
Osmond, C.4
Phipps, K.5
Clark, P.M.6
-
5
-
-
0037622188
-
Fetal sex determination from maternal blood at 6 weeks of gestation when at risk for 21- hydroxylase deficiency
-
Bartha, J. L., Finning, K., & Soothill, P. W. (2003). Fetal sex determination from maternal blood at 6 weeks of gestation when at risk for 21- hydroxylase deficiency. Obstetrics & Gynecology, 101, 1135-1136.
-
(2003)
Obstetrics & Gynecology
, vol.101
, pp. 1135-1136
-
-
Bartha, J.L.1
Finning, K.2
Soothill, P.W.3
-
6
-
-
77949475929
-
Review and meta-analysis: Benefits and risks of multiple courses of antenatal corticosteroids
-
Bevilacqua, E., Brunelli, R., & Anceschi, M. M. (2010). Review and meta-analysis: benefits and risks of multiple courses of antenatal corticosteroids. Journal of Maternal Fetal Neonatal Medicine, 23, 244-260.
-
(2010)
Journal of Maternal Fetal Neonatal Medicine
, vol.23
, pp. 244-260
-
-
Bevilacqua, E.1
Brunelli, R.2
Anceschi, M.M.3
-
7
-
-
66149126549
-
Clinical and molecular characterization of a cohort of 161 unrelated women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency and 330 family members
-
Bidet, M., Bellanné-Chantelot, C., Galand-Portier, M. B., Tardy, V., Billaud, L., Laborde, K., et al. (2009). Clinical and molecular characterization of a cohort of 161 unrelated women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency and 330 family members. Journal of Clinical Endocrinology & Metabolism, 94, 1570-1578.
-
(2009)
Journal of Clinical Endocrinology & Metabolism
, vol.94
, pp. 1570-1578
-
-
Bidet, M.1
Bellanné-Chantelot, C.2
Galand-Portier, M.B.3
Tardy, V.4
Billaud, L.5
Laborde, K.6
-
8
-
-
73949107907
-
Congenital adrenal hyperplasia: A critical appraisal of the evolution of feminizing genitoplasty and the controversies surrounding gender reassignment
-
Braga, L. H., & Pippi Salle, J. L. (2009). Congenital adrenal hyperplasia: a critical appraisal of the evolution of feminizing genitoplasty and the controversies surrounding gender reassignment. European Journal of Pediatric Surgery, 19, 203-210.
-
(2009)
European Journal of Pediatric Surgery
, vol.19
, pp. 203-210
-
-
Braga, L.H.1
Pippi Salle, J.L.2
-
9
-
-
0029670919
-
The ontogeny of 11 betahydroxysteroid dehydrogenase type 2 and mineralocorticoid receptor gene expression reveal intricate control of glucocorticoid action in development
-
Brown, R. W., Diaz, R., Robson, A. C., Kotelevtsev, Y. V., Mullins, J. J., Kaufman, M. H., et al. (1996). The ontogeny of 11 betahydroxysteroid dehydrogenase type 2 and mineralocorticoid receptor gene expression reveal intricate control of glucocorticoid action in development. Endocrinology, 137, 794-797.
-
(1996)
Endocrinology
, vol.137
, pp. 794-797
-
-
Brown, R.W.1
Diaz, R.2
Robson, A.C.3
Kotelevtsev, Y.V.4
Mullins, J.J.5
Kaufman, M.H.6
-
10
-
-
66149158523
-
Reassessing fecundity in women with classical congenital adrenal hyperplasia (CAH): Normal pregnancy rate but reduced fertility rate
-
Casteràs, A., De Silva, P., Rumsby, G., & Conway, G. S. (2009). Reassessing fecundity in women with classical congenital adrenal hyperplasia (CAH): normal pregnancy rate but reduced fertility rate. Clinical Endocrinology (Oxf), 70, 833-837.
-
(2006)
Clinical Endocrinology (Oxf)
, vol.70
, pp. 833-837
-
-
Casteràs, A.1
De Silva, P.2
Rumsby, G.3
Conway, G.S.4
-
11
-
-
0031870574
-
Prenatal dexamethasone causes oligonephria, sodium retention, and higher blood pressure in the offspring
-
Celsi, G., Kistner, A., Aizman, R., Eklöf, A.-C., Ceccatelli, S., de Santiago, A., et al. (1998). Prenatal dexamethasone causes oligonephria, sodium retention, and higher blood pressure in the offspring. Pediatric Research, 4, 317-322.
-
(1998)
Pediatric Research
, vol.4
, pp. 317-322
-
-
Celsi, G.1
Kistner, A.2
Aizman, R.3
Eklöf, A.-C.4
Ceccatelli, S.5
De Santiago, A.6
-
12
-
-
0442307682
-
Reduced maternal dexamethasone dosage for the prenatal treatment of congenital adrenal hyperplasia
-
Coleman, M. A., & Honour, J. W. (2004). Reduced maternal dexamethasone dosage for the prenatal treatment of congenital adrenal hyperplasia. BJOG Int J Obstet Gynecol, 111, 176-178.
-
(2004)
BJOG Int J Obstet Gynecol
, vol.111
, pp. 176-178
-
-
Coleman, M.A.1
Honour, J.W.2
-
13
-
-
77955451907
-
Molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: An update of new CYP21A2 mutations
-
Concolino, P., Mello, E., Zuppi, C., & Capoluongo, E. (2010).Molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: an update of new CYP21A2 mutations. Clinical Chemistry & Laboratory Medicine, 48, 1057-1062.
-
(2010)
Clinical Chemistry & Laboratory Medicine
, vol.48
, pp. 1057-1062
-
-
Concolino, P.1
Mello, E.2
Zuppi, C.3
Capoluongo, E.4
-
14
-
-
0036275355
-
Enhancement of p53 activity and inhibition of neural cell proliferation by glucocorticoid receptor activation
-
Crochemore, C., Michaelidis, T. M., Fischer, D., Loeffler, J. P., & Almeida, O. F. (2002). Enhancement of p53 activity and inhibition of neural cell proliferation by glucocorticoid receptor activation. FASEB Journal, 6, 761-770.
-
(2002)
FASEB Journal
, vol.6
, pp. 761-770
-
-
Crochemore, C.1
Michaelidis, T.M.2
Fischer, D.3
Loeffler, J.P.4
Almeida, O.F.5
-
15
-
-
38849102551
-
Sexual function and genital sensitivity following feminizing genitoplasty for congenital adrenal hyperplasia
-
Crouch, N. S., Liao, L. M., Woodhouse, C. R., Conway, G. S., & Creighton, S. M. (2008). Sexual function and genital sensitivity following feminizing genitoplasty for congenital adrenal hyperplasia. Journal of Urology, 179, 634-638.
-
(2008)
Journal of Urology
, vol.179
, pp. 634-638
-
-
Crouch, N.S.1
Liao, L.M.2
Woodhouse, C.R.3
Conway, G.S.4
Creighton, S.M.5
-
16
-
-
0031440444
-
Population-based case- control study of teratogenic potential of corticosteroids
-
Czeizel, A. E., & Rockenbauer, M. (1997). Population-based case- control study of teratogenic potential of corticosteroids. Teratology, 56, 335-340.
-
(1997)
Teratology
, vol.56
, pp. 335-340
-
-
Czeizel, A.E.1
Rockenbauer, M.2
-
17
-
-
0021691461
-
Prenatal treatment of congenital adrenal hyperplasia resulting from 21-hydroxylase deficiency
-
David, M., & Forest, M. G. (1984). Prenatal treatment of congenital adrenal hyperplasia resulting from 21-hydroxylase deficiency. Journal of Pediatrics, 105, 799-803.
-
(1984)
Journal of Pediatrics
, vol.105
, pp. 799-803
-
-
David, M.1
Forest, M.G.2
-
18
-
-
34147141449
-
Prenatal dexamethasone exposure induces changes in nonhuman primate offspring cardiometabolic and hypothalamic-pituitary-adrenal axis function
-
de Vries, A., Holmes, M. C., Heijnis, A., Seier, J. V., Heerden, J., Louw, J., et al. (2007). Prenatal dexamethasone exposure induces changes in nonhuman primate offspring cardiometabolic and hypothalamic-pituitary-adrenal axis function. Journal of Clinical Investigation, 117, 1058-1067.
-
(2007)
Journal of Clinical Investigation
, vol.117
, pp. 1058-1067
-
-
De Vries, A.1
Holmes, M.C.2
Heijnis, A.3
Seier, J.V.4
Heerden, J.5
Louw, J.6
-
19
-
-
33846259288
-
Maternal dexamethasone treatment at midgestation reduces nephron number and alters renal gene expression in the fetal spiny mouse
-
Dickinson, H., Walker, D. W., Wintour, E. M., & Moritz, K. (2007). Maternal dexamethasone treatment at midgestation reduces nephron number and alters renal gene expression in the fetal spiny mouse. American Journal of Physiology; Regulatory Integrative Comparative Physiology, 292, R453-R461.
-
(2007)
American Journal of Physiology; Regulatory Integrative Comparative Physiology
, vol.292
-
-
Dickinson, H.1
Walker, D.W.2
Wintour, E.M.3
Moritz, K.4
-
20
-
-
0025297224
-
An update on the frequency of nonclassic deficiency of adrenal 21-hydroxylase in the Yugoslav population
-
Dumić, M., Brkljacić, L., Speiser, P. W., Wood, E., Crawford, C., Plavsić, V., et al. (1990). An update on the frequency of nonclassic deficiency of adrenal 21-hydroxylase in the Yugoslav population. Acta Endocrinologica (Copenh)., 122, 703-710.
-
(1990)
Acta Endocrinologica (Copenh).
, vol.122
, pp. 703-710
-
-
Dumić, M.1
Brkljacić, L.2
Speiser, P.W.3
Wood, E.4
Crawford, C.5
Plavsić, V.6
-
21
-
-
0027530474
-
Dysfunction of placental glucocorticoid barrier: Link between fetal environment and adult hypertension?
-
Edwards, C. R., Benediktsson, R., Lindsay, R. S., & Seckl, J. R. (1993). Dysfunction of placental glucocorticoid barrier: link between fetal environment and adult hypertension? Lancet, 341, 355-357.
-
(1993)
Lancet
, vol.341
, pp. 355-357
-
-
Edwards, C.R.1
Benediktsson, R.2
Lindsay, R.S.3
Seckl, J.R.4
-
22
-
-
0026096434
-
Daily cortisol production rate in man determined by stable isotope dilution/mass spectrometry
-
Esteban, N. V., Loughlin, T., Yergey, A. L., Zawadzki, J. K., Booth, J. D., Winterer, J. C., et al. (1991). Daily cortisol production rate in man determined by stable isotope dilution/mass spectrometry. Journal of Clinical Endocrinology & Metabolism, 72, 39-45.
-
(1991)
Journal of Clinical Endocrinology & Metabolism
, vol.72
, pp. 39-45
-
-
Esteban, N.V.1
Loughlin, T.2
Yergey, A.L.3
Zawadzki, J.K.4
Booth, J.D.5
Winterer, J.C.6
-
23
-
-
84944370999
-
Pharmacologic suppression of the fetal adrenal gland in utero. Attempted prevention of abnormal external genital masculinization in suspected congenital adrenal hyperplasia
-
Evans, M. I., Chrousos, G. P., Mann, D.W., Larsen, J.W., Jr., Green, I., McCluskey, J., et al. (1985). Pharmacologic suppression of the fetal adrenal gland in utero. Attempted prevention of abnormal external genital masculinization in suspected congenital adrenal hyperplasia. JAMA, 253, 1015-1020.
-
(1985)
JAMA
, vol.253
, pp. 1015-1020
-
-
Evans, M.I.1
Chrousos, G.P.2
Mann, D.W.3
Larsen Jr., J.W.4
Green, I.5
McCluskey, J.6
-
24
-
-
8844257307
-
Recent advances in the diagnosis and management of congenital adrenal hyperplasia due to 21-hydroxylase deficiency
-
Forest, M. G. (2004). Recent advances in the diagnosis and management of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Human Reproduction Update, 10, 469-485.
-
(2004)
Human Reproduction Update
, vol.10
, pp. 469-485
-
-
Forest, M.G.1
-
25
-
-
0037591676
-
Prenatal therapy in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: Retrospective follow-up study of 253 treated pregnancies in 215 families
-
Forest, M. G., & Dorr, H. G. (2003). Prenatal therapy in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: retrospective follow-up study of 253 treated pregnancies in 215 families. Endocrinologist, 13, 252-259.
-
(2003)
Endocrinologist
, vol.13
, pp. 252-259
-
-
Forest, M.G.1
Dorr, H.G.2
-
26
-
-
0027538375
-
Prenatal diagnosis and treatment of 21-hydroxylase deficiency
-
Forest, M. G., David, M., & Morel, Y. (1993). Prenatal diagnosis and treatment of 21-hydroxylase deficiency. Journal of Steroid Biochemistry & Molecular Biology, 45, 75-82.
-
(1993)
Journal of Steroid Biochemistry & Molecular Biology
, vol.45
, pp. 75-82
-
-
Forest, M.G.1
David, M.2
Morel, Y.3
-
27
-
-
0032171295
-
Prenatal treatment of congenital adrenal hyperplasia
-
Forest, M. G., Morel, Y., & David, M. (1998). Prenatal treatment of congenital adrenal hyperplasia. Trends in Endocrinology & Metabolism, 9, 284-289.
-
(1998)
Trends in Endocrinology & Metabolism
, vol.9
, pp. 284-289
-
-
Forest, M.G.1
Morel, Y.2
David, M.3
-
28
-
-
0001033198
-
Production of congenital defects in the off-spring of pregnant mice treated with cortisone; Progress report
-
Fraser, F. C., & Fainstat, T. D. (1951). Production of congenital defects in the off-spring of pregnant mice treated with cortisone; progress report. Pediatrics, 8, 527-533.
-
(1951)
Pediatrics
, vol.8
, pp. 527-533
-
-
Fraser, F.C.1
Fainstat, T.D.2
-
29
-
-
0028955881
-
Teratogenic potential of corticosteroids in humans
-
Fraser, F. C., & Sajoo, A. (1995). Teratogenic potential of corticosteroids in humans. Teratology, 51, 45-46.
-
(1995)
Teratology
, vol.51
, pp. 45-46
-
-
Fraser, F.C.1
Sajoo, A.2
-
30
-
-
0033673199
-
Technical report: Congenital adrenal hyperplasia
-
Frias, J., Levine, L. S., Oberfield, S. E., Pang, S., Silverstein, J., et al. (2000). Technical report: congenital adrenal hyperplasia. Section on Endocrinology and Committee on Genetics. Pediatrics, 106, 1511-1518.
-
(2000)
Section on Endocrinology and Committee on Genetics. Pediatrics
, vol.106
, pp. 1511-1518
-
-
Frias, J.1
Levine, L.S.2
Oberfield, S.E.3
Pang, S.4
Silverstein, J.5
-
31
-
-
0018279445
-
Human foetal palatal corticoid receptors and teratogens for cleft palate
-
Goldman, A. S., Sharpior, B. H., & Katsumata, M. (1978). Human foetal palatal corticoid receptors and teratogens for cleft palate. Nature, 272, 464-466.
-
(1978)
Nature
, vol.272
, pp. 464-466
-
-
Goldman, A.S.1
Sharpior, B.H.2
Katsumata, M.3
-
32
-
-
33645511061
-
In humans, early cortisol biosynthesis provides a mechanism to safeguard female sexual development
-
Goto, M., Hanley, K. P., Marcos, J., Wood, P. J., Wright, S., Postle, A. D., et al. (2006). In humans, early cortisol biosynthesis provides a mechanism to safeguard female sexual development. Journal of Clinical Investigation, 116, 953-960.
-
(2006)
Journal of Clinical Investigation
, vol.116
, pp. 953-960
-
-
Goto, M.1
Hanley, K.P.2
Marcos, J.3
Wood, P.J.4
Wright, S.5
Postle, A.D.6
-
33
-
-
79952705355
-
Glucocorticoids, prenatal stress and the programming of disease
-
Harris, A., & Seckl, J. (2011). Glucocorticoids, prenatal stress and the programming of disease. Hormones & Behavior, 59, 279- 289.
-
(2011)
Hormones & Behavior
, vol.59
, pp. 279-289
-
-
Harris, A.1
Seckl, J.2
-
34
-
-
33846978755
-
Cognitive functions in children at risk for congenital adrenal hyperplasia treated prenatally with dexamethasone
-
Hirvikoski, T., Nordenstrom, A., Lindholm, T., Lindblad, F., Ritzén, E. M., Wedell, A., et al. (2007). Cognitive functions in children at risk for congenital adrenal hyperplasia treated prenatally with dexamethasone. Journal of Clinical Endocrinology & Metabolism, 92, 542-548.
-
(2007)
Journal of Clinical Endocrinology & Metabolism
, vol.92
, pp. 542-548
-
-
Hirvikoski, T.1
Nordenstrom, A.2
Lindholm, T.3
Lindblad, F.4
Ritzén, E.M.5
Wedell, A.6
-
35
-
-
53249103687
-
Long-termfollow-up of prenatally treated children at risk for congenital adrenal hyperplasia: Does dexamethasone cause behavioural problems?
-
Hirvikoski, T., Nordenstrom, A., Lindholm, F., Ritzén, E. M., & Lajic, S. (2008). Long-termfollow-up of prenatally treated children at risk for congenital adrenal hyperplasia: does dexamethasone cause behavioural problems? European Journal of Endocrinology, 159, 309- 316.
-
(2008)
European Journal of Endocrinology
, vol.159
, pp. 309-316
-
-
Hirvikoski, T.1
Nordenstrom, A.2
Lindholm, F.3
Ritzén, E.M.4
Lajic, S.5
-
36
-
-
80051879901
-
Gender role behaviour in prenatally dexamethasone-treated children at risk for congenital adrenal hyperplasia-A pilot study
-
doi:10.1111/j.1651-2227.2011.02260.x
-
Hirvikoski, T., Lindholm, T., Lajic, S., & Nordenström, A. (2011). Gender role behaviour in prenatally dexamethasone-treated children at risk for congenital adrenal hyperplasia - a pilot study. Acta Paediatrica, 100 (9), e112-e119. doi:10.1111/j.1651-2227.2011.02260.x.
-
(2011)
Acta Paediatrica
, vol.100
, Issue.9
-
-
Hirvikoski, T.1
Lindholm, T.2
Lajic, S.3
Nordenström, A.4
-
37
-
-
84864914283
-
Prenatal dexamethasone treatment of children at risk for congenital adrenal hyperplasia: The Swedish experience and stand-point
-
doi:10.1210/jc.2012-1222
-
Hirvikoski, T., Nordenstrom, A., Wedell, A., Ritzen, & Lajic, S. (2012). Prenatal dexamethasone treatment of children at risk for congenital adrenal hyperplasia: The Swedish experience and stand-point. Journal of Clinical Endocrinology and Metabolism. doi:10.1210/jc.2012-1222.
-
(2012)
Journal of Clinical Endocrinology and Metabolism.
-
-
Hirvikoski, T.1
Nordenstrom, A.2
Ritzen, W.A.3
Lajic, S.4
-
38
-
-
33645582847
-
The mother or the fetus? 11beta-hydroxysteroid dehydrogenase type 2 null mice provide evidence for direct fetal programming of behavior by endogenous glucocorticoids
-
Holmes, M. C., Abrahamsen, C. T., French, K. L., Paterson, J. M., Mullins, J. J., & Seckl, J. R. (2006). The mother or the fetus? 11beta-hydroxysteroid dehydrogenase type 2 null mice provide evidence for direct fetal programming of behavior by endogenous glucocorticoids. Journal of Neuroscience, 26, 3840-3844.
-
(2006)
Journal of Neuroscience
, vol.26
, pp. 3840-3844
-
-
Holmes, M.C.1
Abrahamsen, C.T.2
French, K.L.3
Paterson, J.M.4
Mullins, J.J.5
Seckl, J.R.6
-
39
-
-
0032806268
-
Effect of corticosteroids on brain growth in fetal sheep
-
Huang,W. L., Beazley, L. D., Quinlivan, J. A., Evans, S. F., Newnham, J. P., & Dunlop, S. A. (1999). Effect of corticosteroids on brain growth in fetal sheep. Obstetrics & Gynecology, 94, 213-218.
-
(1999)
Obstetrics & Gynecology
, vol.94
, pp. 213-218
-
-
Huang, W.L.1
Beazley, L.D.2
Quinlivan, J.A.3
Evans, S.F.4
Newnham, J.P.5
Dunlop, S.A.6
-
40
-
-
79958212167
-
Development and function of the human fetal adrenal cortex: A key component in the feto-placental unit
-
Ishimoto, H., & Jaffe, R. B. (2011). Development and function of the human fetal adrenal cortex: a key component in the feto-placental unit. Endocrine Reviews, 32, 317-355.
-
(2011)
Endocrine Reviews
, vol.32
, pp. 317-355
-
-
Ishimoto, H.1
Jaffe, R.B.2
-
41
-
-
18644377699
-
Consensus statement on 21-hydroxylase deficiency from the European Society for Paediatric Endocrinology and the Lawson Wilkins Pediatric Endocrine Society
-
Joint ESPELWPES Working Group (Writing Committee: Clayton PE Miller WL Oberfield SE Ritzen EM Sippell WG Speiser PW)
-
Joint ESPE/LWPES Working Group (Writing Committee: Clayton PE Miller WL, Oberfield SE, Ritzen EM, Sippell WG, Speiser PW) (2002). Consensus statement on 21-hydroxylase deficiency from the European Society for Paediatric Endocrinology and the Lawson Wilkins Pediatric Endocrine Society. Hormone Research, 58, 188- 195.
-
(2002)
Hormone Research
, vol.58
, pp. 188-195
-
-
-
42
-
-
0036726640
-
Consensus statement on 21-hydroxylase deficiency from the Lawson Wilkins Pediatric Endocrine Society and the European Society for Paediatric Endocrinology
-
Joint LWPESESPE CAH Working Group (Writing Committee: Clayton PE Miller WL Oberfield SE Ritzen EM Sippell WG Speiser PW)
-
Joint LWPES/ESPE CAH Working Group (Writing Committee: Clayton PE Miller WL, Oberfield SE, Ritzen EM, Sippell WG, Speiser PW) (2002). Consensus statement on 21-hydroxylase deficiency from The Lawson Wilkins Pediatric Endocrine Society and The European Society for Paediatric Endocrinology. Journal of Clinical Endocrinology & Metabolism, 87, 4048- 4953.
-
(2002)
Journal of Clinical Endocrinology & Metabolism
, vol.87
, pp. 4048-4953
-
-
-
43
-
-
0029996891
-
Serum cortisol, dehydroepiandrosterone sulfate, and sterolbinding globulins in preterm neonates: Effects of gestational age and dexamethasone therapy
-
Kari, M. A., Raivio, K. O., Stenman, U.-H., & Voutilainen, R. (1996). Serum cortisol, dehydroepiandrosterone sulfate, and sterolbinding globulins in preterm neonates: effects of gestational age and dexamethasone therapy. Pediatric Resesarch, 40, 319-324.
-
(1996)
Pediatric Resesarch
, vol.40
, pp. 319-324
-
-
Kari, M.A.1
Raivio, K.O.2
Stenman, U.-H.3
Voutilainen, R.4
-
44
-
-
0027210603
-
Estimation of daily cortisol production and clearance rates in normal pubertal males by deconvolution analysis
-
Kerrigan, J. R., Veldhuis, J. D., Leyo, S. A., Iranmanes, H. A., & Rogol, A. D. (1993). Estimation of daily cortisol production and clearance rates in normal pubertal males by deconvolution analysis. Journal of Clinical Endocrinology & Metabolism, 76, 1505- 1510.
-
(1993)
Journal of Clinical Endocrinology & Metabolism
, vol.76
, pp. 1505-1510
-
-
Kerrigan, J.R.1
Veldhuis, J.D.2
Leyo, S.A.3
Iranmanes, H.A.4
Rogol, A.D.5
-
45
-
-
70350011828
-
Duplications of the functional CYP21A2 gene are primarily restricted to Q318X alleles: Evidence for a founder effect
-
Kleinle, S., Lang, R., Fischer, G. F., Vierhapper, H., Waldhauser, F., Födinger, M., et al. (2009). Duplications of the functional CYP21A2 gene are primarily restricted to Q318X alleles: evidence for a founder effect. Journal of Clinical Endocrinology & Metabolism, 94, 3954-3958.
-
(2009)
Journal of Clinical Endocrinology & Metabolism
, vol.94
, pp. 3954-3958
-
-
Kleinle, S.1
Lang, R.2
Fischer, G.F.3
Vierhapper, H.4
Waldhauser, F.5
Födinger, M.6
-
46
-
-
0036821001
-
Duplication of the CYP21A2 gene complicates mutation analysis of steroid 21-hydroxylase deficiency: Characteristics of three unusual haplotypes
-
Koppens, P. F., Hoogenboezem, T., & Degenhart, H. J. (2002). Duplication of the CYP21A2 gene complicates mutation analysis of steroid 21-hydroxylase deficiency: characteristics of three unusual haplotypes. Human Genetics, 111, 405-410.
-
(2002)
Human Genetics
, vol.111
, pp. 405-410
-
-
Koppens, P.F.1
Hoogenboezem, T.2
Degenhart, H.J.3
-
47
-
-
0031764921
-
Longterm somatic follow-up of prenatally treated children with congenital adrenal hyperplasia
-
Lajic, S.,Wedell, A., Bui, T.-H., Ritzén, E. M.,&Holst, M. (1998). Longterm somatic follow-up of prenatally treated children with congenital adrenal hyperplasia. Journal of Clinical Endocrinology & Metabolism, 83, 3872-3880.
-
(1998)
Journal of Clinical Endocrinology & Metabolism
, vol.83
, pp. 3872-3880
-
-
Lajic, S.1
Wedell, A.2
Bui, T.-H.3
Ritzén, E.M.4
Holst, M.5
-
48
-
-
0025641380
-
Cortisol production rate in childhood and adolescence
-
Linder, B. L., Esteban, N. V., Yergey, A. L.,Winterer, J. C., Loriaux, D. L., & Cassorla, F. (1990). Cortisol production rate in childhood and adolescence. Journal of Pediatrics, 117, 892-896.
-
(1990)
Journal of Pediatrics
, vol.117
, pp. 892-896
-
-
Linder, B.L.1
Esteban, N.V.2
Yergey, L.3
Winterer, A.J.C.4
Loriaux, D.L.5
Cassorla, F.6
-
49
-
-
0029948716
-
Inhibition of 11-beta-hydroxysteroid dehydrogenase in pregnant rats and the programming of blood pressure in the offspring
-
Lindsay, R. S., Lindsay, R. M., Edwards, C. R., & Seckl, J. R. (1996a). Inhibition of 11-beta-hydroxysteroid dehydrogenase in pregnant rats and the programming of blood pressure in the offspring. Hypertension, 27, 1200-1204.
-
(1996)
Hypertension
, vol.27
, pp. 1200-1204
-
-
Lindsay, R.S.1
Lindsay, R.M.2
Edwards, C.R.3
Seckl, J.R.4
-
50
-
-
0029989854
-
Prenatal glucocorticoid exposure leads to offspring hyperglycaemia in the rat: Studies with the 11 beta-hydroxysteroid dehydrogenase inhibitor carbenoxolone
-
Lindsay, R. S., Lindsay, R. M., Waddell, B. J., & Seckl, J. R. (1996b). Prenatal glucocorticoid exposure leads to offspring hyperglycaemia in the rat: studies with the 11 beta-hydroxysteroid dehydrogenase inhibitor carbenoxolone. Diabetologia, 39, 1299-1305.
-
(1996)
Diabetologia
, vol.39
, pp. 1299-1305
-
-
Lindsay, R.S.1
Lindsay, R.M.2
Waddell, B.J.3
Seckl, J.R.4
-
51
-
-
0342618532
-
Presence of fetal DNA in maternal plasma and serum
-
Lo, Y. M., Corbetta, N., Chamberlain, P. F., Rai, V., Sargent, I. L., Redman, C. W., et al. (1997). Presence of fetal DNA in maternal plasma and serum. Lancet, 350, 485-487.
-
(1997)
Lancet
, vol.350
, pp. 485-487
-
-
Lo, Y.M.1
Corbetta, N.2
Chamberlain, P.F.3
Rai, V.4
Sargent, I.L.5
Redman, C.W.6
-
52
-
-
0347898005
-
Quantitative analysis of fetal DNA in maternal plasma and serum: Implications for noninvasive prenatal diagnosis
-
Lo, Y. M., Tein, M. S., Lau, T. K., Haines, C. J., Leung, T. N., Poon, P. M., et al. (1998). Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis. American Journal of Human Genetics, 62, 768-775.
-
(1998)
American Journal of Human Genetics
, vol.62
, pp. 768-775
-
-
Lo, Y.M.1
Tein, M.S.2
Lau, T.K.3
Haines, C.J.4
Leung, T.N.5
Poon, P.M.6
-
53
-
-
0035740121
-
Antenatal glucocorticoids and the developing brain: Mechanisms of action
-
Mathews, S. G. (2001). Antenatal glucocorticoids and the developing brain: mechanisms of action. Seminars in Neonatology, 6, 309- 317.
-
(2001)
Seminars in Neonatology
, vol.6
, pp. 309-317
-
-
Mathews, S.G.1
-
54
-
-
0029006995
-
Prenatal treatment and diagnosis of congenital adrenal hyperplasia owing to 21-hydroxylase deficiency
-
Mercado, A. B., Wilson, R. C., Cheng, K. C., Wei, J. Q., & New, M. I. (1995). Prenatal treatment and diagnosis of congenital adrenal hyperplasia owing to 21-hydroxylase deficiency. Journal of Clinical Endocrinology & Metabolism, 80, 2014-2020.
-
(1995)
Journal of Clinical Endocrinology & Metabolism
, vol.80
, pp. 2014-2020
-
-
Mercado, A.B.1
Wilson, R.C.2
Cheng, K.C.3
Wei, J.Q.4
New, M.I.5
-
55
-
-
1442303408
-
Cognitive and motor development of children with and without congenital adrenal hyperplasia after early-prenatal dexamethasone
-
Meyer-Bahlburg, H. F. L., Dolezal, C., Baker, S. W., Carlson, A. D., Obeid, J. S., & New, M. I. (2004). Cognitive and motor development of children with and without congenital adrenal hyperplasia after early-prenatal dexamethasone. Journal of Clinical Endocrinology & Metabolism, 89, 610-614.
-
(2004)
Journal of Clinical Endocrinology & Metabolism
, vol.89
, pp. 610-614
-
-
Meyer-Bahlburg, H.F.L.1
Dolezal, C.2
Baker, S.W.3
Carlson, A.D.4
Obeid, J.S.5
New, M.I.6
-
56
-
-
0028154269
-
Genetics, diagnosis, and management of 21- hydroxylase deficiency
-
Miller, W. L. (1994). Genetics, diagnosis, and management of 21- hydroxylase deficiency. Journal of Clinical Endocrinology & Metabolism, 78, 241-246.
-
(1994)
Journal of Clinical Endocrinology & Metabolism
, vol.78
, pp. 241-246
-
-
Miller, W.L.1
-
57
-
-
0032832404
-
Dexamethasone treatment of congenital adrenal hyperplasia - An experimental therapy of unproven safety
-
Miller, W. L. (1999). Dexamethasone treatment of congenital adrenal hyperplasia - an experimental therapy of unproven safety. Journal of Urology, 162, 537-540.
-
(1999)
Journal of Urology
, vol.162
, pp. 537-540
-
-
Miller, W.L.1
-
58
-
-
79951665862
-
The molecular biology, biochemistry, and physiology of human steroidogenesis and its disorders
-
Miller, W. L., & Auchus, R. J. (2011). The molecular biology, biochemistry, and physiology of human steroidogenesis and its disorders. Endocrine Reviews, 32, 81-151.
-
(2011)
Endocrine Reviews
, vol.32
, pp. 81-151
-
-
Miller, W.L.1
Auchus, R.J.2
-
59
-
-
0024808985
-
Molecular genetics of 21- hydroxylase deficiency
-
Miller, W. L., & Morel, Y. (1989). Molecular genetics of 21- hydroxylase deficiency. Annual Review of Genetics, 23, 371-393.
-
(1989)
Annual Review of Genetics
, vol.23
, pp. 371-393
-
-
Miller, W.L.1
Morel, Y.2
-
60
-
-
12844276164
-
Effects into adulthood of single or repeated antenatal corticosteroids in sheep
-
Moss, T. J., Doherty, D. A., Nitsos, I., Sloboda, D. M., Harding, R., & Newnham, J. P. (2005). Effects into adulthood of single or repeated antenatal corticosteroids in sheep. American Journal of Obstetrics & Gynecology, 192, 146-152.
-
(2005)
American Journal of Obstetrics & Gynecology
, vol.192
, pp. 146-152
-
-
Moss, T.J.1
Doherty, D.A.2
Nitsos, I.3
Sloboda, D.M.4
Harding, R.5
Newnham, J.P.6
-
61
-
-
57649215365
-
Multiple courses of antenatal corticosteroids for preterm birth (MACS): A randomised controlled trial
-
Murphy, K. E., Hannah, M. E., Willan, A. R., Hewson, S. A., Ohlsson, A., Kelly, E. N., et al. (2008). Multiple courses of antenatal corticosteroids for preterm birth (MACS): a randomised controlled trial. Lancet, 372, 2143-2151.
-
(2008)
Lancet
, vol.372
, pp. 2143-2151
-
-
Murphy, K.E.1
Hannah, M.E.2
Willan, A.R.3
Hewson, S.A.4
Ohlsson, A.5
Kelly, E.N.6
-
62
-
-
79957680673
-
Phenotypic profiling of parents with cryptic nonclassic congenital adrenal hyperplasia: Findings in 145 unrelated families
-
Nandagopal, R., Sinaii, N., Avila, N. A., Van Ryzin, C., Chen, W., Finkielstain, G. P., et al. (2011). Phenotypic profiling of parents with cryptic nonclassic congenital adrenal hyperplasia: findings in 145 unrelated families. European Journal of Endocrinology, 164, 977-984.
-
(2011)
European Journal of Endocrinology
, vol.164
, pp. 977-984
-
-
Nandagopal, R.1
Sinaii, N.2
Avila, N.A.3
Van Ryzin, C.4
Chen, W.5
Finkielstain, G.P.6
-
63
-
-
85047686218
-
Extensive personal experience: Prenatal diagnosis for congenital adrenal hyperplasia in 532 pregnancies
-
New, M. I., Carlson, A., Obeid, J., Marshall, I., Cabrera, M. S., Goseco, A., et al. (2001). Extensive personal experience: prenatal diagnosis for congenital adrenal hyperplasia in 532 pregnancies. Journal of Clinical Endocrinology & Metabolism, 86, 5651-5657.
-
(2001)
Journal of Clinical Endocrinology & Metabolism
, vol.86
, pp. 5651-5657
-
-
New, M.I.1
Carlson, A.2
Obeid, J.3
Marshall, I.4
Cabrera, M.S.5
Goseco, A.6
-
64
-
-
39049131701
-
Type of mutation and surgical procedure affect long-term quality of life for women with congenital adrenal hyperplasia
-
Nordenskjöld, A., Holmdahl, G., Frisén, L., Falhammar, H., Filipsson, H., Thorén, M., et al. (2008). Type of mutation and surgical procedure affect long-term quality of life for women with congenital adrenal hyperplasia. Journal of Clinical Endocrinology & Metabolism, 93, 380-386.
-
(2008)
Journal of Clinical Endocrinology & Metabolism
, vol.93
, pp. 380-386
-
-
Nordenskjöld, A.1
Holmdahl, G.2
Frisén, L.3
Falhammar, H.4
Filipsson, H.5
Thorén, M.6
-
65
-
-
77955391072
-
Sexual function and surgical outcome in women with congenital adrenal hyperplasia due to CYP21A2 deficiency: Clinical perspective and the patients' perception
-
Nordenström, A., Frisén, L., Falhammar, H., Filipsson, H., Holmdahl, G., Janson, P. O., et al. (2010). Sexual function and surgical outcome in women with congenital adrenal hyperplasia due to CYP21A2 deficiency: clinical perspective and the patients' perception. Journal of Clinical Endocrinology & Metabolism, 95, 3633-3640.
-
(2010)
Journal of Clinical Endocrinology & Metabolism
, vol.95
, pp. 3633-3640
-
-
Nordenström, A.1
Frisén, L.2
Falhammar, H.3
Filipsson, H.4
Holmdahl, G.5
Janson, P.O.6
-
66
-
-
0026749953
-
Maternal side-effects of prenatal dexamethasone therapy for fetal congenital adrenal hyperplasia
-
Pang, S., Clark, A. T., Freeman, L. C., Dolan, L. M., Immken, L., Mueller, O. T., et al. (1992). Maternal side-effects of prenatal dexamethasone therapy for fetal congenital adrenal hyperplasia. Journal of Clinical Endocrinology & Metabolism, 75, 249-253.
-
(1992)
Journal of Clinical Endocrinology & Metabolism
, vol.75
, pp. 249-253
-
-
Pang, S.1
Clark, A.T.2
Freeman, L.C.3
Dolan, L.M.4
Immken, L.5
Mueller, O.T.6
-
67
-
-
47749118384
-
High frequency of copy number variations and sequence variants at CYP21A2 locus: Implication for the genetic diagnosis of 21- hydroxylase deficiency
-
Parajes, S., Quinteiro, C., Domínguez, F., & Loidi, L. (2008). High frequency of copy number variations and sequence variants at CYP21A2 locus: implication for the genetic diagnosis of 21- hydroxylase deficiency. PLoS One, 3(5), e2138.
-
(2008)
PLoS One
, vol.3
, Issue.5
-
-
Parajes, S.1
Quinteiro, C.2
Domínguez, F.3
Loidi, L.4
-
68
-
-
0025723923
-
The steroid hormonal milieu of the undisturbed human fetus and mother at 16-20 weeks gestation
-
Partsch, C. J., Sippell, W. G., MacKenzie, I. Z., & Aynsley-Green, A. (1991). The steroid hormonal milieu of the undisturbed human fetus and mother at 16-20 weeks gestation. Journal of Clinical Endocrinology & Metabolism, 73, 969-974.
-
(1991)
Journal of Clinical Endocrinology & Metabolism
, vol.73
, pp. 969-974
-
-
Partsch, C.J.1
Sippell, W.G.2
MacKenzie, I.Z.3
Aynsley-Green, A.4
-
69
-
-
0032952879
-
Repeated, but not single, maternal administration of corticosteroids delays myelination in the brain of fetal sheep
-
Quinlivan, J. A., Dunlop, S. A., Newnham, J. P., Evans, S. F., & Beazley, L. D. (1999). Repeated, but not single, maternal administration of corticosteroids delays myelination in the brain of fetal sheep. Perinat Neonatal Med, 4, 47-55.
-
(1999)
Perinat Neonatal Med
, vol.4
, pp. 47-55
-
-
Quinlivan, J.A.1
Dunlop, S.A.2
Newnham, J.P.3
Evans, S.F.4
Beazley, L.D.5
-
70
-
-
38049048682
-
Recent advances in diagnosis, treatment and outcome of congenital adrenal hyperplasia due to 21-hydroxylase deficiency
-
Reipe, F. G., & Sippell, W. G. (2007). Recent advances in diagnosis, treatment and outcome of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Reviews in Endocrine & Metabolic Disorders, 8, 349-363.
-
(2007)
Reviews in Endocrine & Metabolic Disorders
, vol.8
, pp. 349-363
-
-
Reipe, F.G.1
Sippell, W.G.2
-
71
-
-
84860401478
-
Health problems in congenital adrenal hyperplasia due to 21-hydroxylase deficiency
-
Reisch, N., Arlt, W., & Krone, N. (2011). Health problems in congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Hormone Research in Paediatrics, 76, 73-85.
-
(2011)
Hormone Research in Paediatrics
, vol.76
, pp. 73-85
-
-
Reisch, N.1
Arlt, W.2
Krone, N.3
-
72
-
-
0034818672
-
Fetal sex determination from maternal plasma in pregnancies at risk for congenital adrenal hyperplasia
-
Rijnders, R. J., van der Schoot, C. E., Bossers, B., de Vroede, M. A., & Christiaens, G. C. (2001). Fetal sex determination from maternal plasma in pregnancies at risk for congenital adrenal hyperplasia. Obstetrics & Gynecology, 98, 374-378.
-
(2001)
Obstetrics & Gynecology
, vol.98
, pp. 374-378
-
-
Rijnders, R.J.1
Van Der Schoot, C.E.2
Bossers, B.3
De Vroede, M.A.4
Christiaens, G.C.5
-
73
-
-
0031852122
-
Prenatal treatment of congenital adrenal hyperplasia: A commentary
-
Ritzén, E. M. (1998). Prenatal treatment of congenital adrenal hyperplasia: a commentary. Trends in Endocrinology & Metabolism, 9, 293-295.
-
(1998)
Trends in Endocrinology & Metabolism
, vol.9
, pp. 293-295
-
-
Ritzén, E.M.1
-
74
-
-
0033771823
-
Dexamethasone treatment of virilizing congenital adrenal hyperplasia: The ability to achieve normal growth
-
Rivkees, S. A., & Crawford, J. D. (2000). Dexamethasone treatment of virilizing congenital adrenal hyperplasia: the ability to achieve normal growth. Pediatrics, 106, 767-773.
-
(2000)
Pediatrics
, vol.106
, pp. 767-773
-
-
Rivkees, S.A.1
Crawford, J.D.2
-
75
-
-
0028043830
-
Malformation surveillance and maternal drug exposure: The MADRE project
-
Robert, E., Vollset, S. E., Botto, L., Lancaster, P. A. L., Merlob, P., Mastroiacovo, P., et al. (1994). Malformation surveillance and maternal drug exposure: the MADRE project. Risk Safety Med, 6, 78-118.
-
(1994)
Risk Safety Med
, vol.6
, pp. 78-118
-
-
Robert, E.1
Vollset, S.E.2
Botto, L.3
Lancaster, P.A.L.4
Merlob, P.5
Mastroiacovo, P.6
-
76
-
-
0031689424
-
Corticosteroids during pregnancy and oral clefts: A case-control study
-
Rodriguez-Pinilla, E., & Martinez-Frias, M. L. (1998). Corticosteroids during pregnancy and oral clefts: a case-control study. Teratology, 58, 2-5.
-
(1998)
Teratology
, vol.58
, pp. 2-5
-
-
Rodriguez-Pinilla, E.1
Martinez-Frias, M.L.2
-
78
-
-
0031795257
-
The efficacy of methylprednisolone in the treatment of hyperemesis gravidarum: A randomized, doubleblind, controlled study
-
Safari, H. R., Fassett, M. J., Souter, I. C., Alsulyman, O. M., & Goodwin, T. M. (1998). The efficacy of methylprednisolone in the treatment of hyperemesis gravidarum: a randomized, doubleblind, controlled study. American Journal of Obstetrics & Gynecology, 179, 921-924.
-
(1998)
American Journal of Obstetrics & Gynecology
, vol.179
, pp. 921-924
-
-
Safari, H.R.1
Fassett, M.J.2
Souter, I.C.3
Alsulyman, O.M.4
Goodwin, T.M.5
-
79
-
-
80053629817
-
Nongenomic glucocorticoid receptor action regulates gap junction intercellular communication and neural progenitor cell proliferation. Proceedings National
-
Samarasinghe, R. A., Di Maio, R., Volonte, D., Galbiati, F., Lewis, M., Romero, G., et al. (2011). Nongenomic glucocorticoid receptor action regulates gap junction intercellular communication and neural progenitor cell proliferation. Proceedings National Academy of Science (U S A), 108(40), 16657-16662.
-
(2011)
Academy of Science (U S A)
, vol.108
, Issue.40
, pp. 16657-16662
-
-
Samarasinghe, R.A.1
Di Maio, R.2
Volonte, D.3
Galbiati, F.4
Lewis, M.5
Romero, G.6
-
80
-
-
10344226154
-
Prenatal glucocorticoids and long-term programming
-
Seckl, J. R. (2004). Prenatal glucocorticoids and long-term programming. European Journal of Endocrinology, 151, U49-U62.
-
(2004)
European Journal of Endocrinology
, vol.151
-
-
Seckl, J.R.1
-
81
-
-
0030961591
-
How safe is long-term prenatal glucocorticoid treatment?
-
Seckl, J. R., & Miller, W. L. (1997). How safe is long-term prenatal glucocorticoid treatment? JAMA, 277, 1077-1079.
-
(1997)
JAMA
, vol.277
, pp. 1077-1079
-
-
Seckl, J.R.1
Miller, W.L.2
-
82
-
-
17844406864
-
Synthetic glucocorticoids: Antenatal administration and long-term implications
-
Sloboda, D. M., Challis, J. R. G., Moss, T. J. M., & Newnham, J. P. (2005). Synthetic glucocorticoids: antenatal administration and long-term implications. Current Pharmaceutical Design, 11, 1459-1472.
-
(2005)
Current Pharmaceutical Design
, vol.11
, pp. 1459-1472
-
-
Sloboda, D.M.1
Challis, J.R.G.2
Moss, T.J.M.3
Newnham, J.P.4
-
83
-
-
77956424486
-
Prenatal treatment of classic CAH with dexamethasone: Pro vs. con
-
Speiser, P.W., & Miller,W. L. (2008). Prenatal treatment of classic CAH with dexamethasone: pro vs. con. Endocrine News, 33, 15-18.
-
(2008)
Endocrine News
, vol.33
, pp. 15-18
-
-
Speiser, P.W.1
Miller, W.L.2
-
85
-
-
0022219639
-
High frequency of nonclassical steroid 21- hydroxylase deficiency
-
Speiser, P. W., Dupont, B., Rubinstein, P., Piazza, A., Kastelan, A., & New, M. I. (1985). High frequency of nonclassical steroid 21- hydroxylase deficiency. American Journal of Human Genetics, 37, 650-667.
-
(1985)
American Journal of Human Genetics
, vol.37
, pp. 650-667
-
-
Speiser, P.W.1
Dupont, B.2
Rubinstein, P.3
Piazza, A.4
Kastelan, A.5
New, M.I.6
-
86
-
-
0026576532
-
Genotype of Yupik Eskimos with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
-
Speiser, P. W., New, M. I., Tannin, G. M., Pickering, D., Yang, S. Y., & White, P. C. (1992). Genotype of Yupik Eskimos with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Human Genetics, 88, 647-648.
-
(1992)
Human Genetics
, vol.88
, pp. 647-648
-
-
Speiser, P.W.1
New, M.I.2
Tannin, G.M.3
Pickering, D.4
Yang, S.Y.5
White, P.C.6
-
87
-
-
77956588420
-
Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: An Endocrine Society clinical practice guideline
-
Speiser, P. W., Azziz, R., Baskin, L. S., Ghizzoni, L., Hensle, T. W., Merke, D. P., et al. (2010). Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society clinical practice guideline. Journal of Clinical Endocrinology & Metabolism, 95, 4133-4160.
-
(2010)
Journal of Clinical Endocrinology & Metabolism
, vol.95
, pp. 4133-4160
-
-
Speiser, P.W.1
Azziz, R.2
Baskin, L.S.3
Ghizzoni, L.4
Hensle, T.W.5
Merke, D.P.6
-
88
-
-
0001836060
-
Growth patterns in congenital adrenal hyperplasia - Correlation of glucocorticoid therapy with stature
-
P. Lee, L. Plotnick, A. Kowarski, & C. Migeon (Eds.), Baltimore: University Park Press
-
Styne, D. M., Richards, G. E., Bell, J. J., Conte, F. A., Morishima, A., Kaplan, S. L., et al. (1977). Growth patterns in congenital adrenal hyperplasia - Correlation of glucocorticoid therapy with stature. In P. Lee, L. Plotnick, A. Kowarski, & C. Migeon (Eds.), Congenital adrenal hyperplasia (pp. 247-261). Baltimore: University Park Press.
-
(1977)
Congenital Adrenal Hyperplasia
, pp. 247-261
-
-
Styne, D.M.1
Richards, G.E.2
Bell, J.J.3
Conte, F.A.4
Morishima, A.5
Kaplan, S.L.6
-
89
-
-
56049100045
-
Prenatal diagnosis and treatment of steroid 21-hydroxylase deficiency
-
Tajima, T., & Fujieda, K. (2008). Prenatal diagnosis and treatment of steroid 21-hydroxylase deficiency. Clinical Pediatric Endocrinology, 17, 95-102.
-
(2008)
Clinical Pediatric Endocrinology
, vol.17
, pp. 95-102
-
-
Tajima, T.1
Fujieda, K.2
-
90
-
-
2642620230
-
Results of screening 1.9 million Texas newborns for 21-hydroxylase- deficient congenital adrenal hyperplasia
-
Therrell, B. L., Jr., Berenbaum, S. A., Manter-Kapanke, V., Simmank, J., Korman, K., Prentice, L., et al. (1998). Results of screening 1.9 million Texas newborns for 21-hydroxylase-deficient congenital adrenal hyperplasia. Pediatrics, 101, 583-590.
-
(1998)
Pediatrics
, vol.101
, pp. 583-590
-
-
Therrell Jr., B.L.1
Berenbaum, S.A.2
Manter-Kapanke, V.3
Simmank, J.4
Korman, K.5
Prentice, L.6
-
91
-
-
0025270537
-
Brain damage induced by prenatal exposure to dexamethasone in fetal rhesus macaques. I. Hippocampus
-
Uno, H., Lohmiller, L., Thieme, C., Kemnitz, J.W., Engle,M. J., Roeker, E. B., et al. (1990). Brain damage induced by prenatal exposure to dexamethasone in fetal rhesus macaques. I. Hippocampus. Developmental Brain Research, 53, 157-167.
-
(1990)
Developmental Brain Research
, vol.53
, pp. 157-167
-
-
Uno, H.1
Lohmiller, L.2
Thieme, C.3
Kemnitz, J.W.4
Engle, M.J.5
Roeker, E.B.6
-
92
-
-
0037045438
-
Maternal cigarette smoking, metabolic gene polymorphism, and infant birth weight
-
Wang, X., Zuckerman, B., Pearson, C., Kaufman, G., Chen, C., Wang, G., et al. (2002). Maternal cigarette smoking, metabolic gene polymorphism, and infant birth weight. JAMA, 287, 195-202.
-
(2002)
JAMA
, vol.287
, pp. 195-202
-
-
Wang, X.1
Zuckerman, B.2
Pearson, C.3
Kaufman, G.4
Chen, C.5
Wang, G.6
-
94
-
-
0031046241
-
11β-hydroxysteroid dehydrogenase and the syndrome of apparent mineralocorticoid excess
-
White, P. C., Mune, T., & Agarwal, A. K. (1997). 11β- hydroxysteroid dehydrogenase and the syndrome of apparent mineralocorticoid excess. Endocrine Reviews, 18, 135-156.
-
(1997)
Endocrine Reviews
, vol.18
, pp. 135-156
-
-
White, P.C.1
Mune, T.2
Agarwal, A.K.3
-
95
-
-
33947592785
-
Ethnic-specific distribution of mutations in 716 patients with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency
-
Wilson, R. C.,Nimkarn, S., Dumić, M.,Obeid, J., Azar,M.R., Najmabadi, H., et al. (2007). Ethnic-specific distribution of mutations in 716 patients with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency. Molecular Genetics & Metabolism, 90, 414-421.
-
(2007)
Molecular Genetics & Metabolism
, vol.90
, pp. 414-421
-
-
Wilson, C.1
Nimkarn, R.S.2
Dumić, M.3
Obeid, J.4
Azar, M.R.5
Najmabadi, H.6
-
96
-
-
79956131423
-
Congenital adrenal hyperplasia
-
Witchel, S. F., & Azziz, R. (2011). Congenital adrenal hyperplasia. Journal of Pediatric & Adolescent Gynecology, 24(3), 116-126.
-
(2011)
Journal of Pediatric & Adolescent Gynecology
, vol.24
, Issue.3
, pp. 116-126
-
-
Witchel, S.F.1
Azziz, R.2
|