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New England Journal of Medicine, ISSN 0028-4793, 02/2008, Volume 358, Issue 7, pp. 709 - 715
Journal Article
Endocrine Reviews, ISSN 0163-769X, 07/2019, Volume 40, Issue 6, pp. 1547 - 1572
Differences/Disorders of sex development (DSD) are a heterogeneous group of congenital conditions that result in discordance between an individual's sex... 
Journal Article
Fertility and Sterility, ISSN 0015-0282, 01/2019, Volume 111, Issue 1, pp. 7 - 12
Women with classic congenital adrenal hyperplasia (CAH) can suffer from impaired fertility rates as a result of increased androgen secretion or impaired sex... 
fertility | Congenital adrenal hyperplasia | reproduction | PROGESTERONE | HOMOZYGOUS MUTATION | FOLLOW-UP | BETA-HYDROXYSTEROID DEHYDROGENASE | PREGNANCY | OBSTETRICS & GYNECOLOGY | WOMEN | P450 OXIDOREDUCTASE | REPRODUCTIVE BIOLOGY | HYDROXYLASE DEFICIENCY | 3-BETA-HYDROXYSTEROID DEHYDROGENASE-DEFICIENCY | GONADAL-FUNCTION
Journal Article
The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 03/2019, Volume 104, Issue 7, pp. 2827 - 2841
Context: Primary ovarian insufficiency (POI) is a cause of female infertility. However, the genetic etiology of this disorder remains unknown in most patients... 
FOLLICULAR DEVELOPMENT | GROWTH | BIOLOGY | ENDOCRINOLOGY & METABOLISM | MICE | MUTATIONS | EXPRESSION | HYPOGONADISM | RNA-POLYMERASE-III | SUBUNIT
Journal Article
Clinical Genetics, ISSN 0009-9163, 09/2019, Volume 96, Issue 3, pp. 261 - 265
Journal Article
Clinics (Sao Paulo, Brazil), ISSN 1807-5932, 12/2018, Volume 73, Issue suppl 1, p. e756
Malignancy must be considered in the management of adrenal lesions, including those incidentally identified on imaging studies. Adrenocortical carcinomas... 
Adrenocortical Carcinoma | Paraganglioma | Pheochromocytoma | Treatment | Review
Journal Article
Journal of Clinical Endocrinology and Metabolism, ISSN 0021-972X, 06/2019, Volume 104, Issue 6, pp. 2112 - 2120
Delta-like homolog 1 (DLK1), also called preadipocyte factor 1, prevents adipocyte differentiation and has been considered a molecular gatekeeper of... 
Journal Article
Journal of Pediatric Endocrinology and Metabolism, ISSN 0334-018X, 01/2018, Volume 31, Issue 2, pp. 223 - 228
Journal Article
Clinical Cancer Research, ISSN 1078-0432, 06/2019, Volume 25, Issue 11, pp. 3276 - 3288
Adrenocortical carcinoma (ACC) is a rare, aggressive malignancy with few therapies; however, patients with locoregional disease have variable outcomes. The... 
Journal Article
Journal of Pediatric Endocrinology and Metabolism, ISSN 0334-018X, 02/2019, Volume 32, Issue 2, pp. 173 - 179
Background: When evaluating peripubertal short stature patients, the interpretation of insulin-like growth factor 1 (IGF-1) levels based on chronological age... 
evaluation | positive predictive value | test performance | GH deficiency | diagnosis | short stature | IGF-1 | STATEMENT | TESTS | GUIDELINES | FACTOR-I | PREVALENCE | ADOLESCENCE | CHILDHOOD | PREPUBERTAL CHILDREN | ENDOCRINOLOGY & METABOLISM | PEDIATRICS | BINDING PROTEIN-3 | GROWTH-HORMONE DEFICIENCY
Journal Article
The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 10/2019
Abstract Context No consensus exists for optimization of mineralocorticoid therapy in patients with primary adrenal insufficiency. Objective To explore the... 
Journal Article
Clinical Genetics, ISSN 0009-9163, 11/2018, Volume 94, Issue 5, pp. 489 - 490
Androgen insensitivity syndrome (AIS) is caused by defects in the androgen receptor (AR) gene and is the most common aetiology of 46,XY disorders of sex... 
INSENSITIVITY SYNDROME | GENETICS & HEREDITY | Genetic research | Genetic engineering | Messenger RNA | Analysis | Androgens | Conserved sequence | Nucleotide sequence | Splicing | Clonal deletion | Transcription | Androgen receptors | Regulatory sequences | Gene deletion | Prostate | Blood | DNA sequencing
Journal Article