1.
Gender Role Behavior, Sexuality, and Psychosocial Adaptation in Women with Congenital Adrenal Hyperplasia due to CYP21A2 Deficiency
by Frisén, Louise
The journal of clinical endocrinology and metabolism, 2009-09, Vol.94 (9), p.3432-3439
2.
Sensitive Monogenic Noninvasive Prenatal Diagnosis by Targeted Haplotyping
by Vermeulen, Carlo
American journal of human genetics, 2017-09-07, Vol.101 (3), p.326-339
3.
Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline
by Speiser, Phyllis W
The journal of clinical endocrinology and metabolism, 2010-09, Vol.95 (9), p.4133-4160
4.
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
5.
Increased Cardiovascular and Metabolic Morbidity in Patients With 21-Hydroxylase Deficiency: A Swedish Population-Based National Cohort Study
by Falhammar, Henrik
The journal of clinical endocrinology and metabolism, 2015-09, Vol.100 (9), p.3520-3528
6.
Combined Loss of the GATA4 and GATA6 Transcription Factors in Male Mice Disrupts Testicular Development and Confers Adrenal-Like Function in the Testes
by Padua, Maria B
Endocrinology (Philadelphia), 2015-05, Vol.156 (5), p.1873-1886
7.
Leydig cell genes change their expression and association with polysomes in a stage-specific manner in the adult mouse testis
by Jauregui, Estela J
Biology of reproduction, 2018-05, Vol.98 (5), p.722-738
8.
Increased Psychiatric Morbidity in Men With Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
by Falhammar, Henrik
The journal of clinical endocrinology and metabolism, 2014-03, Vol.99 (3), p.E554-E560
9.
Genotype-Phenotype Correlation in 153 Adult Patients With Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency: Analysis of the United Kingdom Congenital Adrenal Hyperpl...
by Krone, Nils
The journal of clinical endocrinology and metabolism, 2013-02, Vol.98 (2), p.E346-E354
10.
Genetic Disruption of 21-Hydroxylase in Zebrafish Causes Interrenal Hyperplasia
by Eachus, Helen
Endocrinology (Philadelphia), 2017-12-01, Vol.158 (12), p.4165-4173
11.
Comprehensive Genetic Analysis of 182 Unrelated Families with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
by Finkielstain, Gabriela P
The journal of clinical endocrinology and metabolism, 2011-01, Vol.96 (1), p.E161-E172
12.
Suboptimal Psychosocial Outcomes in Patients With Congenital Adrenal Hyperplasia: Epidemiological Studies in a Nonbiased National Cohort in Sweden
by Strandqvist, A
The journal of clinical endocrinology and metabolism, 2014-04, Vol.99 (4), p.1425-1432
13.
Sexual Function and Surgical Outcome in Women with Congenital Adrenal Hyperplasia Due to CYP21A2 Deficiency: Clinical Perspective and the Patients’ Perception
by Nordenström, Anna
The journal of clinical endocrinology and metabolism, 2010-08, Vol.95 (8), p.3633-3640
14.
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
15.
Type of Mutation and Surgical Procedure Affect Long-Term Quality of Life for Women with Congenital Adrenal Hyperplasia
by Nordenskjöld, Agneta
The journal of clinical endocrinology and metabolism, 2008-02, Vol.93 (2), p.380-386
16.
Prenatal Diagnosis of Congenital Adrenal Hyperplasia Caused by P450 Oxidoreductase Deficiency
by Reisch, Nicole
The journal of clinical endocrinology and metabolism, 2013-03, Vol.98 (3), p.E528-E536
17.
Approach to the Patient: The Adult With Congenital Adrenal Hyperplasia
by Auchus, Richard J
The journal of clinical endocrinology and metabolism, 2013-07, Vol.98 (7), p.2645-2655
18.
Fertility in Women with Nonclassical Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
by Bidet, Maud
The journal of clinical endocrinology and metabolism, 2010-03, Vol.95 (3), p.1182-1190
19.
Biology of the Adrenal Gland Cortex Obviates Effective Use of Adeno-Associated Virus Vectors to Treat Hereditary Adrenal Disorders
by Markmann, Sandra
Human gene therapy, 2018-04-01, Vol.29 (4), p.43-412
20.
Urine Steroid Hormone Profile Analysis in Cytochrome P450 Oxidoreductase Deficiency: Implication for the Backdoor Pathway to Dihydrotestosterone
by Homma, Keiko
The journal of clinical endocrinology and metabolism, 2006-07, Vol.91 (7), p.2643-2649
