Keyphrases
TSH Receptor
50%
Longitudinal Assessment
50%
Adrenal Cortex
50%
Fetal Adrenal
50%
Graves' Disease
50%
Endothelin Receptor Antagonist
50%
Insulin Detemir
50%
Detemir
50%
Joint Research
50%
Parental Diabetes
50%
Adolescent Diabetes
50%
Tall Stature
50%
Histidase
50%
Serum Creatine Kinase
50%
Medical Treatment
50%
Neonatal Diabetes Mellitus
50%
Familial Glucocorticoid Deficiency
50%
Maturity-onset Diabetes of the Young
50%
Children with Type 1 Diabetes
50%
Virilization
50%
Analogue Insulin
50%
Salt Wasting
50%
Piglet Model
50%
Adolescents with Type 1 Diabetes
50%
Insulin Delivery Systems
50%
Prader
50%
21-Hydroxylase Deficiency (21OHD)
50%
External Genitalia
50%
Laparoendoscopic Single-site Surgery
50%
Laparoendoscopic Single-site
50%
Gonadectomy
50%
Testicular Morphology
50%
Hydroxyl Radical Scavengers
50%
Gonadal Dysgenesis
50%
Idic(Y)
50%
SLC26A7
50%
Diagnostic Potential
50%
SLC26A4
50%
TSHR Gene
50%
Thyrotropin Receptor
50%
Hereditary Orotic Aciduria
50%
KMT2D
50%
Uridine Monophosphate
50%
Shwachman-Diamond Syndrome
50%
Lipocortin-1
50%
Kabuki Syndrome
50%
Pediatric Diabetes
50%
Factor Mobility
37%
ACTH Receptor
33%
Growth Failure
33%
Medicine and Dentistry
Endothelin Receptor Antagonist
100%
Steroid 21 Monooxygenase Deficiency
100%
Diabetes
100%
Pediatrics
86%
Pediatrics Patient
56%
Hypovitaminosis D
50%
Vitamin D Deficiency
50%
Oxidative Stress
50%
Thiazide Diuretic Agent
50%
Adrenal Cortex
50%
ABC Transporter Subfamily G
50%
Insulin Detemir
50%
Histidine Ammonialyase
50%
Neonatal Diabetes Mellitus
50%
Insulin Dependent Diabetes Mellitus
50%
Virilization
50%
Salt Wasting
50%
Laparoendoscopic Single Site Surgery
50%
Chromosome Mosaicism
50%
Turner Syndrome
50%
Gonadectomy
50%
Adolescent
50%
Monocarboxylate Transporter 8
50%
Congenital Hypothyroidism
50%
Kallmann Syndrome
50%
Nephrogenic Diabetes Insipidus
50%
Karyotype 45,X
50%
Mixed Gonadal Dysgenesis
50%
Hydroxyl Radical
50%
Fulminant
50%
Neonatal Sepsis
50%
Bartter Syndrome
50%
Insulin Treatment
50%
Shwachman Syndrome
50%
Syndrome CHARGE
50%
Kabuki Syndrome
50%
Desmopressin
50%
Patient with Diabetes
50%
Hypoglycemia
50%
Pediatric Endocrinology
41%
Disease
37%
Hydroperoxide
31%
Sitosterol
25%
Campesterol
25%
Interleukin 6
25%
Mass Screening
25%
Leydig Cell
25%
Trichlormethiazide
25%
Symptom
19%
Antioxidant
18%
Biochemistry, Genetics and Molecular Biology
Mouse
62%
Exon
58%
Glucokinase
50%
Thyroid Function
50%
Insulin Analog
50%
Monospecific Antibody
50%
ABCC8
50%
Testis Development
50%
Selected Ion Monitoring
50%
Aldosterone
50%
Thyrotropin Receptor
50%
Molecular Cloning
50%
21-Hydroxylase
50%
Virilization
50%
Molecular Genetics
50%
Annexin
50%
Glycemic Control
50%
Amnion Fluid
50%
Bartter Syndrome
50%
Genetic Disorder
50%
CHD7
50%
Thyroid Hormone Synthesis
50%
Receptor Gene
50%
Pendrin
50%
Uridine Monophosphate
50%
Desmopressin
50%
Shwachman-Diamond Syndrome
50%
Genetics
35%
Proband
33%
Genotype Phenotype Correlation
33%
ACTH Receptor
28%
Steroid Urine Level
25%
Drug Dose
25%
Recessive Gene
25%
Hemoglobin A
25%
Campesterol
21%
Infancy
20%
Thyroid Hormone
20%
SBDS
18%
Autosomal Recessive Disorder
16%
Next Generation Sequencing
16%
Pregnancy
16%
Autosomal Dominant Inheritance
16%
Gingiva
16%
Hypercalciuria
16%
Hyponatremia
16%
Enzyme Inactivation
16%
Hypomagnesemia
16%
Autosomal Recessive Inheritance
16%
Sanger Sequencing
16%
