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KIMBERLY DRENSER, MD
MD
Retina Specialist (Ophthalmology) Physician
NPI: 1508894643IndividualAccepts Medicare
Specialties, Licenses & Credentials
Ophthalmology Physician
Ophthalmology
Code: 207W00000X
4301081731(MI)
Retina Specialist (Ophthalmology) PhysicianPrimary
Ophthalmology — Retina Specialist
Code: 207WX0107X
4301081731(MI)
CMS Specialties
PrimaryOPHTHALMOLOGY
Education
UNIVERSITY OF FLORIDA COLLEGE OF MEDICINE
Class of 1999
Research & Publications (20)
Elevated levels of cystatin C and tenascin-C in schisis cavities of patients with congenital X-linked retinoschisis.
PMID 18040250·Retina·2007
8-other
Genetic evaluation to establish the diagnosis of X-linked familial exudative vitreoretinopathy.
PMID 17050281·Ophthalmic Genet·2006
8-other
Diagnostic and therapeutic challenges. Progressive bilateral visual loss over the last seven years.
PMID 16141868·Retina·2005
5-case
Norrin attenuates protease-mediated death of transformed retinal ganglion cells.
PMID 19137075·Mol Vis·2009
7-preclinical
Anti-angiogenic therapy in the management of retinopathy of prematurity.
PMID 19494656·Dev Ophthalmol·2009
6-review
Surgical outcomes of epiretinal membranes associated with combined hamartoma of the retina and retinal pigment epithelium.
PMID 19276871·Retina·2009
8-other
Repair of primary rhegmatogenous retinal detachment using 25-gauge transconjunctival sutureless vitrectomy.
PMID 18463517·Retina·2008
8-other
Treatment of vascularly active familial exudative vitreoretinopathy with pegaptanib sodium (Macugen).
PMID 18317351·Retina·2008
5-case
Plasmin enzyme-assisted vitrectomy for primary and reoperated eyes with stage 5 retinopathy of prematurity.
PMID 18317350·Retina·2008
8-other
Vitreous levels of stromal cell-derived factor 1 and vascular endothelial growth factor in patients with retinopathy of prematurity.
PMID 18031819·Ophthalmology·2008
8-other
Plasmin enzyme-assisted vitreoretinal surgery in congenital X-linked retinoschisis: surgical techniques based on a new classification system.
PMID 18040249·Retina·2007
8-other
Pediatric traumatic macular hole: results of autologous plasmin enzyme-assisted vitrectomy.
PMID 17870044·Am J Ophthalmol·2007
8-other
Familial exudative vitreoretinopathy and osteoporosis-pseudoglioma syndrome caused by a mutation in the LRP5 gene.
PMID 17353424·Arch Ophthalmol·2007
8-other
Retinal phenotype-genotype correlation of pediatric patients expressing mutations in the Norrie disease gene.
PMID 17296899·Arch Ophthalmol·2007
8-other
Intraschisis cavity fluid composition in congenital X-linked retinoschisis.
PMID 16946681·Retina·2006
5-case
Ribozyme rescue of photoreceptor cells in P23H transgenic rats: long-term survival and late-stage therapy.
PMID 11005848·Proc Natl Acad Sci U S A·2000
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 3555 W 13 MILE RD, LL-20
ROYAL OAK, MI 48073 - Phone
- (248) 288-2280
Quick Facts
- NPI
- 1508894643
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 27
- Publications
- 20
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