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ELIZABETH NAYLOR, MD
MD
Dermatology Physician
NPI: 1376702761Individual
Specialties, Licenses & Credentials
Dermatology PhysicianPrimary
Dermatology
Code: 207N00000X
35.132169(OH)01087959A(IN)
Research & Publications (20)
A limited spectrum of phenylalanine hydroxylase mutations is observed in phenylketonuria patients in western Poland and implications for treatment with 6R tetrahydrobiopterin.
PMID 19444284·J Hum Genet·2009
8-other
Identification of a chemical probe for NAADP by virtual screening.
PMID 19234453·Nat Chem Biol·2009
7-preclinical
Biochemical characterization of mutant phenylalanine hydroxylase enzymes and correlation with clinical presentation in hyperphenylalaninaemic patients.
PMID 18937047·J Inherit Metab Dis·2009
8-other
Nephrogenic systemic fibrosis with septal panniculitis mimicking erythema nodosum.
PMID 18158925·J Am Acad Dermatol·2008
5-case
Mutations in the phenylalanine hydroxylase gene identified in 95 patients with phenylketonuria using novel systems of mutation scanning and specific genotyping based upon thermal melt profiles.
PMID 17502162·Mol Genet Metab·2007
8-other
Haemophilus influenzae induces neutrophil necrosis: a role in chronic obstructive pulmonary disease?
PMID 17363778·Am J Respir Cell Mol Biol·2007
8-other
The use of filter paper-dried blood spots for thyroid-antibody screening in adults.
PMID 15614253·J Lab Clin Med·2004
8-other
A high throughput beta-globin genotyping method by multiplexed melting temperature analysis.
PMID 14972330·Mol Genet Metab·2004
8-other
Effect of expanded newborn screening for biochemical genetic disorders on child outcomes and parental stress.
PMID 14625333·JAMA·2003
8-other
Use of tandem mass spectrometry for multianalyte screening of dried blood specimens from newborns.
PMID 14578311·Clin Chem·2003
6-review
Assays for thyroid-stimulating hormone using dried blood spotted filter paper specimens to screen for hypothyroidism in older children and adults.
PMID 12790308·J Med Screen·2003
8-other
How do people with Type 2 diabetes perceive and respond to cardiovascular risk?
PMID 12752483·Diabet Med·2003
8-other
Real time PCR assays to detect common mutations in the biotinidase gene and application of mutational analysis to newborn screening for biotinidase deficiency.
PMID 12618081·Mol Genet Metab·2003
8-other
Neonatal blood carnitine concentrations: normative data by electrospray tandem mass spectometry.
PMID 12612202·Pediatr Res·2003
8-other
Analysis of common mutations in the galactose-1-phosphate uridyl transferase gene: new assays to increase the sensitivity and specificity of newborn screening for galactosemia.
PMID 12552079·J Mol Diagn·2003
8-other
Superior venocaval obstruction secondary to central venous catheter-related thromboses in two patients with metastatic colorectal carcinoma receiving weekly 5-flurouracil. Should adjusted-dose warfarin be used as thromboprophylaxis?
PMID 12441915·Blood Coagul Fibrinolysis·2002
5-case
Mitochondrial fatty acid oxidation disorders in Thai infants: a report of 3 cases.
PMID 12403251·J Med Assoc Thai·2002
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
- 2111 E STATE ST
ATHENS, OH 45701 - Phone
- (740) 566-4621
Quick Facts
- NPI
- 1376702761
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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