Back to Search
PAUL S. CLAYTON M.D.
M.D.
Anesthesiology Physician
NPI: 1710055116Individual
Specialties, Licenses & Credentials
Anesthesiology PhysicianPrimary
Anesthesiology
Code: 207L00000X
ME25356(FL)
Research & Publications (20)
The pyrolysis of (-)-(S)-nicotine: racemization and decomposition.
PMID 19644958·Chirality·2010
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
Ten novel HMGCL mutations in 24 patients of different origin with 3-hydroxy-3-methyl-glutaric aciduria.
PMID 19177531·Hum Mutat·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
Analysis of mutant DNA polymerase gamma in patients with mitochondrial DNA depletion.
PMID 18828154·Hum Mutat·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
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
Candidate endophenotypes for genetic studies of suicidal behavior.
PMID 19201395·Biol Psychiatry·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
How the mid-Victorians worked, ate and died.
PMID 19440443·Int J Environ Res Public Health·2009
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
X-linked isolated growth hormone deficiency: expanding the phenotypic spectrum of SOX3 polyalanine tract expansions.
PMID 19654509·Clin Dysmorphol·2009
5-case
25-Hydroxyvitamin D levels in prevalent Australian dialysis patients.
PMID 19619182·Nephrology (Carlton)·2009
8-other
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
Genotype-phenotype correlation in PEX5-deficient peroxisome biogenesis defective cell lines.
PMID 18712838·Hum Mutat·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
Escitalopram: an open-label study of bereavement-related depression and grief.
PMID 18597854·J Affect Disord·2009
2-rct
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
Skewed X inactivation is associated with phenotype in a female with adrenal hypoplasia congenita.
PMID 18762570·J Med Genet·2008
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
- 6500 W NEWBERRY RD
GAINESVILLE, FL 32605 - Phone
- (352) 333-4180
Quick Facts
- NPI
- 1710055116
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
Are you this provider?
Claim Your Profile