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PAIGE CLAYTON, MD
MD
Family Medicine Physician
NPI: 1942792726IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
036157838(IL)
CMS Specialties
PrimaryFAMILY PRACTICE
Education
OTHER
Class of 2018
Research & Publications (20)
Comprehensive description of the phenotype of the first case of congenital disorder of glycosylation due to RFT1 deficiency (CDG In).
PMID 19267216·J Inherit Metab Dis·2009
5-case
How the mid-Victorians worked, ate and died.
PMID 19440443·Int J Environ Res Public Health·2009
8-other
An unsuitable and degraded diet? Part one: public health lessons from the mid-Victorian working class diet.
PMID 18515775·J R Soc Med·2008
8-other
Mutations in the sterol 27-hydroxylase gene (CYP27A) cause hepatitis of infancy as well as cerebrotendinous xanthomatosis.
PMID 12555943·J Inherit Metab Dis·2002
5-case
Applications of mass spectrometry in the study of inborn errors of metabolism.
PMID 11405336·J Inherit Metab Dis·2001
6-review
Hyperinsulinism in short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance of beta-oxidation in insulin secretion.
PMID 11489939·J Clin Invest·2001
5-case
Clinical consequences of defects in peroxisomal beta-oxidation.
PMID 11356171·Biochem Soc Trans·2001
6-review
Safety issues in children and adolescents during growth hormone therapy--a review.
PMID 11161961·Growth Horm IGF Res·2000
6-review
Diagnosis of growth hormone deficiency in childhood. On behalf of the Growth Hormone Research Society.
PMID 10971100·Horm Res·2000
8-other
The pyrolysis of (-)-(S)-nicotine: racemization and decomposition.
PMID 19644958·Chirality·2010
8-other
Inflammatory markers and growth in South Asian and European origin infants in Britain: the Manchester Children's Growth and Vascular Health Study.
PMID 19439300·Atherosclerosis·2009
4-observational
The primordial growth disorder 3-M syndrome connects ubiquitination to the cytoskeletal adaptor OBSL1.
PMID 19481195·Am J Hum Genet·2009
8-other
Expanding the spectrum of mutations in GH1 and GHRHR: genetic screening in a large cohort of patients with congenital isolated growth hormone deficiency.
PMID 19567534·J Clin Endocrinol Metab·2009
8-other
25-Hydroxyvitamin D levels in prevalent Australian dialysis patients.
PMID 19619182·Nephrology (Carlton)·2009
8-other
X-linked isolated growth hormone deficiency: expanding the phenotypic spectrum of SOX3 polyalanine tract expansions.
PMID 19654509·Clin Dysmorphol·2009
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 363 N WEST ST
OLNEY, IL 62450 - Phone
- (618) 392-9400
Quick Facts
- NPI
- 1942792726
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 8
- Publications
- 20
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