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PAUL MATTHEW CLAYTON MD
MD
Emergency Medicine Physician
NPI: 1144884701IndividualAccepts Medicare
Specialties, Licenses & Credentials
Emergency Medicine PhysicianPrimary
Emergency Medicine
Code: 207P00000X
LL82313(SC)
Education
UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL SCHOOL OF MEDICINE
Class of 2019
Research & Publications (20)
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
An unsuitable and degraded diet? Part two: realities of the mid-Victorian diet.
PMID 18591688·J R Soc Med·2008
8-other
Growth hormone replacement throughout life: insights into age-related responses to treatment.
PMID 17560153·Growth Horm IGF Res·2007
6-review
Consensus statement on the management of the GH-treated adolescent in the transition to adult care.
PMID 15745921·Eur J Endocrinol·2005
6-review
Difficulties in patient management associated with the transition period.
PMID 16286777·Horm Res·2005
8-other
Growth hormone signal transduction and possible defects in children.
PMID 12511008·J Pediatr Endocrinol Metab·2002
8-other
The pyrolysis of (-)-(S)-nicotine: racemization and decomposition.
PMID 19644958·Chirality·2010
8-other
Analysis of mutant DNA polymerase gamma in patients with mitochondrial DNA depletion.
PMID 18828154·Hum Mutat·2009
8-other
A pilot study to evaluate gene expression profiles in peripheral blood mononuclear cells (PBMCs) from children with GH deficiency and Turner syndrome in response to GH treatment.
PMID 19018778·Clin Endocrinol (Oxf)·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
Commentary: Out of the silence: confronting depression in medical students and residents.
PMID 19174657·Acad Med·2009
8-other
Genotype-phenotype correlation in PEX5-deficient peroxisome biogenesis defective cell lines.
PMID 18712838·Hum Mutat·2009
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
Candidate endophenotypes for genetic studies of suicidal behavior.
PMID 19201395·Biol Psychiatry·2009
8-other
Escitalopram: an open-label study of bereavement-related depression and grief.
PMID 18597854·J Affect Disord·2009
2-rct
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
A PEX10 defect in a patient with no detectable defect in peroxisome assembly or metabolism in cultured fibroblasts.
PMID 19127411·J Inherit Metab Dis·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
- EMERGENCY MEDICINE DEPARTMENT, 14 MEDICAL PARK, STE 350
COLUMBIA, SC 29203 - Phone
- (803) 434-7088
Quick Facts
- NPI
- 1144884701
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 7
- Publications
- 20
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