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PAUL CLAYTON, MD
MD
Anesthesiology Physician
NPI: 1821191701Individual
Specialties, Licenses & Credentials
Anesthesiology PhysicianPrimary
Anesthesiology
Code: 207L00000X
165462-1205(UT)
Research & Publications (20)
The pyrolysis of (-)-(S)-nicotine: racemization and decomposition.
PMID 19644958·Chirality·2010
8-other
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
Physician use of electronic medical records: issues and successes with direct data entry and physician productivity.
PMID 16779018·AMIA Annu Symp Proc·2005
8-other
Building a comprehensive clinical information system from components. The approach at Intermountain Health Care.
PMID 12695790·Methods Inf Med·2003
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
Clinical consequences of defects in peroxisomal beta-oxidation.
PMID 11356171·Biochem Soc Trans·2001
6-review
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
25-Hydroxyvitamin D levels in prevalent Australian dialysis patients.
PMID 19619182·Nephrology (Carlton)·2009
8-other
The primordial growth disorder 3-M syndrome connects ubiquitination to the cytoskeletal adaptor OBSL1.
PMID 19481195·Am J Hum Genet·2009
8-other
Likelihood of persistent GH deficiency into late adolescence: relationship to the presence of an ectopic or normally sited posterior pituitary gland.
PMID 19226266·Clin Endocrinol (Oxf)·2009
8-other
A nonsense mutation in COQ9 causes autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency: a potentially treatable form of mitochondrial disease.
PMID 19375058·Am J Hum Genet·2009
8-other
Congenital disorder of glycosylation type Ia: heterogeneity in the clinical presentation from multivisceral failure to hyperinsulinaemic hypoglycaemia as leading symptoms in three infants with phosphomannomutase deficiency.
PMID 19396570·J Inherit Metab Dis·2009
5-case
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
How the mid-Victorians worked, ate and died.
PMID 19440443·Int J Environ Res Public Health·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
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
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 9660 S 1300E
SANDY, UT 84094 - Phone
- (801) 993-9582
Quick Facts
- NPI
- 1821191701
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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