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21-hydroxylase deficiency congenital adrenal hyperplasia
Maria I. New
Research output
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Contribution to journal
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Short survey
›
peer-review
39
Scopus citations
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Dive into the research topics of '21-hydroxylase deficiency congenital adrenal hyperplasia'. Together they form a unique fingerprint.
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Keyphrases
21-hydroxylase
14%
21-Hydroxylase Deficiency (21OHD)
100%
Autosomal Recessive
14%
Chorionic Villus Sampling
14%
Clinical Expression
14%
Clinical Presentation
14%
Common Disease
14%
Congenital Adrenal Hyperplasia
100%
Cortisol
14%
Decision Basis
14%
Disease Course
14%
Early Pregnancy
14%
Encoding Gene
14%
Endocrine Disorders
28%
Enzyme Deficiency
14%
Etiology
14%
Genotype
14%
Molecular Genetics
14%
Molecular Treatment
14%
Prenatal Diagnosis
14%
Prenatal Treatment
14%
Specific mutation
14%
Steroidogenic Enzymes
14%
Structural Genes
14%
Therapeutic Decision-making
14%
Medicine and Dentistry
21-Hydroxylase
14%
Autosomal Recessive Inheritance
14%
Chorionic Villus Sampling
14%
Clinician
14%
Congenital Adrenal Hyperplasia
100%
Disease
28%
Endocrine Disease
28%
Enzyme Defect
14%
First Trimester Pregnancy
14%
Hydrocortisone
14%
Molecular Diagnosis
14%
Prenatal Diagnosis
14%
Steroid 21 Monooxygenase Deficiency
100%
Steroidogenic Enzymes
14%
Structural Gene
14%
Biochemistry, Genetics and Molecular Biology
21-Hydroxylase
100%
Autosomal Recessive Inheritance
25%
Chorion Villus
25%
Cortisol
25%
Enzyme
25%
First Trimester Pregnancy
25%
Genotyping
25%
Molecular Genetics
25%
Steroidogenic Enzymes
25%
Structural Gene
25%
Pharmacology, Toxicology and Pharmaceutical Science
21-Hydroxylase
14%
Congenital Adrenal Hyperplasia
100%
Disease
28%
Endocrine Disease
28%
Enzyme Defect
14%
Hydrocortisone
14%
Steroid 21 Monooxygenase Deficiency
100%