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KRISTIN WULFF, MD
MD
Surgery Physician
NPI: 1285771444IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine Physician
Family Medicine
Code: 207Q00000X
ME104612(FL)
Surgery PhysicianPrimary
Surgery
Code: 208600000X
ME104612(FL)
CMS Specialties
PrimaryFAMILY PRACTICE
Additional
PERIPHERAL VASCULAR DISEASE
Education
PENNSYLVANIA STATE UNIVERSITY COLLEGE OF MEDICINE
Class of 2002
Research & Publications (20)
Identification of a novel large F9 gene mutation-an insertion of an Alu repeated DNA element in exon e of the factor 9 gene.
PMID 10679958·Hum Mutat·2000
8-other
Sleep and circadian rhythm disturbances: multiple genes and multiple phenotypes.
PMID 19423332·Curr Opin Genet Dev·2009
6-review
Blue light-filtering intraocular lenses: review of potential benefits and side effects.
PMID 19545821·J Cataract Refract Surg·2009
6-review
Factor VII deficiency: clinical manifestation of 717 subjects from Europe and Latin America with mutations in the factor 7 gene.
PMID 18976247·Haemophilia·2009
4-observational
Hereditary angioedema caused by missense mutations in the factor XII gene: clinical features, trigger factors, and therapy.
PMID 19477491·J Allergy Clin Immunol·2009
8-other
Delayed sleep phase in severe obsessive-compulsive disorder: a systematic case-report survey.
PMID 18496478·CNS Spectr·2008
5-case
Variability of clinical manifestation of factor VII-deficiency in homozygous and heterozygous subjects of the European F7 gene mutation A294V.
PMID 18556408·Haematologica·2008
8-other
An adaptive system identification approach to optical trap calibration.
PMID 18542538·Opt Express·2008
8-other
Three-dimensional parallel holographic micropatterning using a spatial light modulator.
PMID 18825231·Opt Express·2008
8-other
Analysis of the novel factor X gene mutation Glu51Lys in two families with factor X-Riyadh anomaly.
PMID 17393015·Thromb Haemost·2007
8-other
Short-wavelength light sensitivity of circadian, pupillary, and visual awareness in humans lacking an outer retina.
PMID 18082405·Curr Biol·2007
5-case
Long-term FVII substitution in a preterm infant with severe gastrointestinal bleeding and FVII deficiency due to a homozygous donor splice mutation IVS4+1G-->A.
PMID 16651241·Pediatr Hematol Oncol·2006
5-case
Common polymorphisms and cardiovascular factors in patients with myocardial infarction of Costa Rica.
PMID 18457169·Rev Biol Trop·2006
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
- 1630 MASON AVE STE C
DAYTONA BEACH, FL 32117 - Phone
- (386) 238-9064
Quick Facts
- NPI
- 1285771444
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 24
- Publications
- 20
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