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Congenital adrenal hyperplasia owing to 11β-hydroxylase deficiency
Perrin C. White
Pediatrics
Endocrinology
Research output
:
Chapter in Book/Report/Conference proceeding
›
Chapter
4
Scopus citations
Overview
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Dive into the research topics of 'Congenital adrenal hyperplasia owing to 11β-hydroxylase deficiency'. Together they form a unique fingerprint.
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Medicine & Life Sciences
Cytochrome P-450 CYP11B2
100%
Steroid 11-beta-Hydroxylase
89%
Congenital Adrenal Hyperplasia
88%
Mixed Function Oxygenases
75%
Desoxycorticosterone
29%
Aldosterone
23%
Oxidoreductases
20%
Glucocorticoid-Remediable Aldosteronism
19%
Hydrocortisone
19%
Cortodoxone
17%
Genetic Crossing Over
15%
Hyperkalemia
13%
Genes
13%
Hyponatremia
13%
Nucleic Acid Regulatory Sequences
12%
Mutation
12%
Enzymes
12%
Corticosterone
11%
Isoenzymes
11%
Adrenocorticotropic Hormone
11%
Angiotensin II
10%
Potassium
10%
Shock
9%
Hypertension
7%
Chemical Compounds
Aldosterone
94%
Cortisol
34%
Steroid
24%
Mutation
22%
11-Deoxycorticosterone
22%
11-Deoxycortisol
22%
Corticosterone
18%
Angiotensin II
16%
Disorder
11%