- ►annals.org DP Merke, SR Bornstein, NA Avila, GP … - Annals of internal …, 2002 - Am Coll Physicians Congenital adrenal hyperplasia describes a group of inherited autosomal recessive disorders
characterized by an enzymatic defect in cortisol biosynthesis, compensatory increases in
corticotropin secretion, and ... Cited by 81 - Related articles - All 4 versions
DP Merke, GP Chrousos, G Eisenhofer, M … - The New England …, 2000 - nejm.highwire.org Results Plasma epinephrine and metanephrine concentrations and urinary epinephrine excretion were 40
to 80 percent lower in the patients with congenital adrenal hyperplasia than in the normal subjects
(P< 0.05), and the values were ... Cited by 90 - Related articles - BL Direct - All 6 versions
- ►endojournals.org E Charmandari, G Eisenhofer, SL Mehlinger, A … - Journal of Clinical …, 2002 - Endocrine Soc Classic congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is characterized by
decreased synthesis of glucocorticoids and mineralocorticoids, adrenal hyperandrogenism, and
impaired development and function ... Cited by 26 - Related articles - BL Direct - All 9 versions
- ►endojournals.org MS Cabrera, MG Vogiatzi, MI New - Journal of Clinical Endocrinology & …, 2001 - Endocrine Soc The effects of classic congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency on
final height and fertility were evaluated in 30 affected males, aged 17–43 yr. The mean adult
height of these patients was 165.64 ... Cited by 89 - Related articles - BL Direct - All 4 versions
- ►endojournals.org NMML Stikkelbroeck, WJG Oyen, GJ van der … - Journal of Clinical …, 2003 - Endocrine Soc Patients with congenital adrenal hyperplasia attributable to 21-hydroxylase deficiency are treated
with glucocorticoids. Glucocorticoid administration, even in substitution doses, may cause decreased
bone mineral density (BMD) and ... Cited by 34 - Related articles - BL Direct - All 5 versions
- ►endojournals.org DP Merke, MF Keil, JV Jones, J Fields, S Hill, … - Journal of Clinical …, 2000 - Endocrine Soc Treatment outcome in congenital adrenal hyperplasia is often suboptimal due to hyperandrogenism,
treatment-induced hypercortisolism, or both. We previously reported better control of linear growth,
weight gain, and bone maturation in ... Cited by 67 - Related articles - BL Direct - All 7 versions
DP Merke, GB Cutler - Endocrinology and metabolism clinics of North America, 2001 - Elsevier Dramatic improvement has occurred in the lives of patients with congenital adrenal hyperplasia (CAH)
during the past 50 years through the introduction of glucocorticoid and mineralocorticoid
replacement therapy 18 and ... Cited by 29 - Related articles - BL Direct - All 4 versions
- ►endojournals.org DF Gunther, TP Bukowski, EM Ritzen, A Wedell, … - Journal of Clinical …, 1997 - Endocrine Soc Long term follow-up studies of children with congenital adrenal hyperplasia have documented less
than desirable outcomes, including reduction in final adult height, obesity, virilism, and decreased
fertility. We have proposed that ... Cited by 30 - Related articles - BL Direct - All 6 versions
EF Roche, E Charmandari, MT Dattani, PC … - Clinical …, 2003 - interscience.wiley.com It is also possible that your web browser is not configured or not able to display style sheets. In
this case, although the visual presentation will be degraded, the site should continue to be
functional. We recommend using the ... Cited by 25 - Related articles - BL Direct - All 4 versions
