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Extensive clinical experience: Nonclassical 21-hydroxylase deficiency
Maria I. New
Friedman Brain Institute
Genetics and Genomic Sciences
Icahn School of Medicine at Mount Sinai
Pediatrics
Research output
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Contribution to journal
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Article
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peer-review
290
Scopus citations
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Keyphrases
Hyperandrogenic
100%
Congenital Adrenal Hyperplasia
100%
21-Hydroxylase Deficiency (21OHD)
100%
Clinical Experience
100%
Hirsutism
50%
Nonclassical Congenital Adrenal Hyperplasia
50%
Ashkenazi Jews
50%
New York City
50%
Autosomal Recessive
50%
Ambiguous Genitalia
50%
Male Patients
50%
Female Patients
50%
Moderate to Severe
50%
Short Stature
50%
Ethnic Groups
50%
Non-associated
50%
Infertility
50%
Adult Female
50%
Precocious Puberty
50%
Genetic Disease
50%
Hyperandrogenism
50%
Acne
50%
Polycystic Ovary
50%
Adult Male
50%
Tall Stature
50%
Endocrine Abnormalities
50%
Child Growth
50%
Dexamethasone Treatment
50%
City Population
50%
Pubic Hair
50%
Testicular Adrenal Rest Tumors
50%
Menstrual Period
50%
Classical Form
50%
Advanced Bone Age
50%
Medicine and Dentistry
Congenital Adrenal Hyperplasia
100%
Steroid 21 Monooxygenase Deficiency
100%
Disease
33%
Dexamethasone
33%
Hirsutism
33%
Polycystic Ovary Syndrome
33%
Neonatal Infant
33%
Ambiguous Genitalia
33%
Short Stature
33%
Autosomal Recessive Inheritance
33%
Ethnic Group
33%
Bone Age
33%
Genetic Disorder
33%
Physical Disease by Body Function
33%
Hyperandrogenism
33%
Menstrual Cycle
33%
Urban Population
33%
Tall Stature
33%
Precocious Puberty
33%
Acne Cystica
33%
Pharmacology, Toxicology and Pharmaceutical Science
Congenital Adrenal Hyperplasia
100%
Steroid 21 Monooxygenase Deficiency
100%
Disease
33%
Dexamethasone
33%
Ovary Polycystic Disease
33%
Hirsutism
33%
Ambiguous Genitalia
33%
Precocious Puberty
33%
Physical Disease by Body Function
33%
Hyperandrogenism
33%
Genetic Disorder
33%
Short Stature
33%
Tall Stature
33%
Acne Cystica
33%