1.
Noninvasive Prenatal Diagnosis of Congenital Adrenal Hyperplasia Using Cell-Free Fetal DNA in Maternal Plasma
by New, Maria I
The journal of clinical endocrinology and metabolism, 2014-06, Vol.99 (6), p.E1022-E1030
2.
Sexual Orientation in Women with Classical or Non-classical Congenital Adrenal Hyperplasia as a Function of Degree of Prenatal Androgen Excess
by Meyer-Bahlburg, Heino F. L
Archives of sexual behavior, 2007-12-22, Vol.37 (1), p.85-99
3.
Final Adult Height in Children with Congenital Adrenal Hyperplasia Treated with Growth Hormone
by Lin-Su, Karen
The journal of clinical endocrinology and metabolism, 2011-06, Vol.96 (6), p.1710-1717
4.
Stigma Associated with Classical Congenital Adrenal Hyperplasia in Women’s Sexual Lives
by Meyer-Bahlburg, Heino F. L
Archives of sexual behavior, 2017-05-18, Vol.47 (4), p.943-951
5.
Extensive clinical experience: nonclassical 21-hydroxylase deficiency
by New, Maria I
The journal of clinical endocrinology and metabolism, 2006-11, Vol.91 (11), p.4205-4214
6.
Syndrome-Related Stigma in the General Social Environment as Reported by Women with Classical Congenital Adrenal Hyperplasia
by Meyer-Bahlburg, Heino F. L
Archives of sexual behavior, 2016-09-27, Vol.46 (2), p.341-351
7.
Prenatal Diagnosis and Treatment of Congenital Adrenal Hyperplasia
by Nimkarn, Saroj
Hormone research, 2007-02, Vol.67 (2), p.53-60
8.
Congenital lipoid adrenal hyperplasia (a rare form of adrenal insufficiency and ambiguous genitalia) caused by a novel mutation of the steroidogenic acute regulatory protein gene
by Lekarev, Oksana
European journal of pediatrics, 2011-11-15, Vol.171 (5), p.787-793
9.
Prenatal androgenization affects gender-related behavior but not gender identity in 5-12-year-old girls with congenital adrenal hyperplasia
by Meyer-Bahlburg, Heino F L
Archives of sexual behavior, 2004-04, Vol.33 (2), p.97-104
10.
Steroid 11-beta hydroxylase deficiency caused by compound heterozygosity for a novel mutation in intron 7 (IVS 7 DS+4A to G) in one CYP11B1 allele and R448H in exon 8 in the other
by Dumic, Katja
European journal of pediatrics, 2009-12-22, Vol.169 (7), p.891-894
11.
Report of Fertility in a Woman with a Predominantly 46,XY Karyotype in a Family with Multiple Disorders of Sexual Development
by Dumic, Miroslav
The journal of clinical endocrinology and metabolism, 2008-01, Vol.93 (1), p.182-189
12.
The Clinical and Molecular Heterogeneity of 17βHSD-3 Enzyme Deficiency
by George, Minu M
Hormone research in paediatrics, 2010-10, Vol.74 (4), p.229-240
13.
Reviewer Critique of “Apparent Mineralocorticoid Excess Manifested in an Elderly Patient With Hypothyroidism”
by Nimkarn, Saroj
American journal of hypertension, 2007, Vol.20 (1), p.108-108
14.
Gender development in women with congenital adrenal hyperplasia as a function of disorder severity
by Meyer-Bahlburg, Heino F L
Archives of sexual behavior, 2006-12, Vol.35 (6), p.667-684
15.
Treatment with Growth Hormone and Luteinizing Hormone Releasing Hormone Analog Improves Final Adult Height in Children with Congenital Adrenal Hyperplasia
by Lin-Su, Karen
The journal of clinical endocrinology and metabolism, 2005-06, Vol.90 (6), p.3318-3325
16.
Long term outcome in adult males with classic congenital adrenal hyperplasia
by CABRERA, Monina S
The journal of clinical endocrinology and metabolism, 2001, Vol.86 (7), p.3070-3078
17.
Aldosterone-to-Renin Ratio as a Marker for Disease Severity in 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia
by Nimkarn, Saroj
The journal of clinical endocrinology and metabolism, 2007-01, Vol.92 (1), p.137-142
18.
DIAGNOSIS AND MANAGEMENT OF CONGENITAL ADRENAL HYPERPLASIA
by New, MD, Maria I
Annual review of medicine, 1998-02, Vol.49 (1), p.311-328
19.
Congenital adrenal hyperplasia in adults
by Lin-Su, Karen
Expert Review of Endocrinology & Metabolism, 2009-01-01, Vol.4 (1), p.67-77
20.
Nonclassical 21-Hydroxylase Deficiency
by New, Maria I
The journal of clinical endocrinology and metabolism, 2006-11, Vol.91 (11), p.4205-4214
