Keyphrases
11β-hydroxysteroid Dehydrogenase
11%
21-Hydroxylase Deficiency (21OHD)
23%
Adult Patients
11%
Affected Females
13%
Agonist Treatment
9%
Androgen Production
9%
Apparent Mineralocorticoid Excess
41%
Autosomal Recessive
10%
Cell-free Fetal DNA
11%
Clinical Diagnosis
8%
Combined Stimulation
8%
Congenital Adrenal Hyperplasia
100%
Cortisol
8%
CYP21A2 Gene
8%
CYP21A2 mutations
8%
Early Adulthood
8%
Endocrine Disorders
17%
Endocrine Emergencies
11%
Etiology
8%
Female Fetus
12%
Fetal DNA in Maternal Plasma
9%
Gender-affirming Hormone Therapy
9%
Genital
11%
Genital Ambiguity
13%
Genotype-phenotype
10%
Gonadotropin-releasing Hormone
10%
Growth Hormone
23%
Growth Hormone Deficiency
13%
Growth Hormone Stimulation Test
18%
Growth Hormone Treatment
9%
Hormone Response
11%
Hydroxysteroid Dehydrogenase
23%
Hypertension
11%
Kindred
16%
Mineralocorticoid
9%
Neonatology
8%
Nonclassical Congenital Adrenal Hyperplasia
9%
Noninvasive Prenatal Diagnosis
21%
Novel mutation
9%
Older Adults
10%
Peak Growth
11%
Prenatal Diagnosis
18%
Salt Wasting
11%
Severe Hypertension
10%
Sex Steroid Priming
8%
Short Stature
13%
Small-for-gestational Age
8%
Spermatogenesis
8%
Stimulation Test
9%
Transgender
16%
Medicine and Dentistry
Adenocarcinoma
8%
Adrenalectomy
8%
Ambiguous Genitalia
14%
Androgen Synthesis
9%
Apparent Mineralocorticoid Excess Syndrome
24%
Autosomal Recessive Inheritance
5%
CA-125
5%
Carcinoma
8%
Cell-Free Fetal DNA
11%
Congenital Adrenal Hyperplasia
90%
Dexamethasone
17%
Diseases
6%
Endocrine Disease
17%
Endocrinology
8%
Ethosuximide
8%
Fertility Preservation
8%
Glucocorticoid
11%
Growth Hormone
25%
Growth Hormone Deficiency
11%
Hormone Deficiency
8%
Hormone Therapy
9%
Hydrocortisone
23%
Hydroxysteroid Dehydrogenase
7%
Hypoglycemia
8%
Hypophysis Hormone
8%
Infancy
8%
Intensive Care
8%
Krukenberg Tumor
8%
Maternal Plasma
9%
Melanocortin 2 Receptor
6%
Mineralocorticoid
8%
Neonate
8%
Neonatology
8%
Organogenesis
5%
Pediatrics
6%
Pelvic Magnetic Resonance Imaging
5%
Prenatal Diagnosis
34%
Prenatal Diagnostics
5%
Quality of Life
8%
Receptor
10%
Salt Wasting
10%
Sex Hormone
8%
Short Stature
12%
Small for Gestational Age
8%
Spermiogenesis
8%
Steroid 21 Monooxygenase Deficiency
18%
Systematic Review
8%
Transgender
16%
Transitional Care
8%
Virilization
6%
Biochemistry, Genetics and Molecular Biology
17-Beta-Hydroxysteroid Dehydrogenase
8%
21-Hydroxylase
26%
Agonist
8%
Autosomal Recessive Disorder
7%
Autosomal Recessive Inheritance
11%
Blood Plasma
11%
Bovine Somatotropin
19%
Cortisol
11%
Deep Sequencing
8%
Deficiency
52%
Dexamethasone
23%
Dideoxynucleotide Sequencing
7%
Enzyme
18%
Exon
5%
First Trimester Pregnancy
8%
Genetic Prenatal Diagnosis
8%
Genetics
23%
Genotyping
7%
Glucocorticoid
8%
Gonadotropin-Releasing Hormone
8%
Growth Hormone
19%
Hydroxysteroid Dehydrogenase
22%
Menarche
8%
Mineralocorticoid
35%
Molecular Genetics
14%
Steroid Biosynthesis
11%
Virilization
8%
