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Abnormal cholesterol metabolism in Smith-Lemli-Opitz syndrome
E. R. Elias
*
, M. Irons
*
Corresponding author for this work
Research output
:
Contribution to journal
›
Review article
›
peer-review
20
Scopus citations
Overview
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Dive into the research topics of 'Abnormal cholesterol metabolism in Smith-Lemli-Opitz syndrome'. Together they form a unique fingerprint.
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Medicine and Dentistry
Cholesterol
100%
Smith-Lemli-Opitz Syndrome
100%
Cholesterol Metabolism
100%
Patient
42%
Congenital Malformation
28%
Precursor
28%
7 Dehydrocholesterol
28%
Development
14%
Cell Function
14%
Diagnosis
14%
Water-Electrolyte Imbalance
14%
Clinical Finding
14%
Persistent Truncus Arteriosus
14%
Autosomal Recessive Disorder
14%
Biosynthesis
14%
Cleft Palate
14%
Association
14%
Child
14%
Health
14%
Childhood
14%
Human
14%
Limb
14%
Plasma
14%
Failure to Thrive
14%
INIS
metabolism
100%
cholesterol
100%
defects
50%
levels
37%
patients
37%
precursor
25%
congenital diseases
25%
humans
12%
children
12%
nervous system diseases
12%
failures
12%
usa
12%
plasma
12%
accumulation
12%
heart disease
12%
errors
12%
limbs
12%
europe
12%
birth
12%
Biochemistry, Genetics and Molecular Biology
Cholesterol
100%
Cholesterol Metabolism
100%
Precursor
40%
Cholesterol Level
40%
7-Dehydrocholesterol
40%
Development
20%
Cell Function
20%
Cholesterol Blood Level
20%
Human
20%
Anabolism
20%
Mental Retardation
20%
Health
20%
Association
20%
Childhood
20%
Birth
20%
Neuroscience
Cholesterol
100%
Smith Lemli Opitz Syndrome
100%
7 Dehydrocholesterol
25%
Cell Function
12%
Cardiovascular System
12%
Palate
12%
Cleft
12%