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GILLIAN WOODRUFF, MD
MD
Internal Medicine Physician
NPI: 1598394496Individual
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
A192204(CA)
Research & Publications (20)
The prevalence of nystagmus: the Leicestershire nystagmus survey.
PMID 19458336·Invest Ophthalmol Vis Sci·2009
8-other
Phenotypical characteristics of idiopathic infantile nystagmus with and without mutations in FRMD7.
PMID 18372314·Brain·2008
4-observational
Sequential leukemic infiltration and human herpesvirus optic neuropathy in acute lymphoblastic leukemia.
PMID 18329931·J AAPOS·2008
5-case
Ethnic variations in the incidence and outcome of severe retinopathy of prematurity.
PMID 17891200·Can J Ophthalmol·2007
8-other
Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus.
PMID 17013395·Nat Genet·2006
8-other
Ophthalmic pathology of genotypically confirmed von Hippel Lindau disease type 1.
PMID 16424542·Br J Ophthalmol·2006
5-case
The importance of seeking ALMS1 mutations in infants with dilated cardiomyopathy.
PMID 15689433·J Med Genet·2005
8-other
Bilateral retinal phototoxic injury during cataract surgery in a child.
PMID 15226731·J AAPOS·2004
5-case
Immune recovery disease: a case of interstitial keratitis and tonic pupil following bone marrow transplantation.
PMID 15548824·Br J Ophthalmol·2004
5-case
Ocular manifestations of mosaic trisomy 22: a case report and review of the literature.
PMID 15255116·Ophthalmic Genet·2004
5-case
Trends in the incidence of severe retinopathy of prematurity in a geographically defined population over a 10-year period.
PMID 15173486·Pediatrics·2004
8-other
Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11q.
PMID 15024691·Am J Hum Genet·2004
8-other
Identification of a fourth locus (EVR4) for familial exudative vitreoretinopathy (FEVR).
PMID 14737064·Mol Vis·2004
8-other
Rapid onset childhood cataracts leading to the diagnosis of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy.
PMID 14597064·Am J Ophthalmol·2003
5-case
An early-onset autosomal dominant macular dystrophy (MCDR3) resembling North Carolina macular dystrophy maps to chromosome 5.
PMID 12714659·Invest Ophthalmol Vis Sci·2003
8-other
Central retinal vein occlusion associated with Sturge Weber syndrome.
PMID 12194091·Eye (Lond)·2002
5-case
Exogenous Pseudomonas endophthalmitis: a cause of lens enucleation.
PMID 11978756·Arch Dis Child Fetal Neonatal Ed·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
Via practice · 2 locations total
- Address
- 5800 Hollis St
Emeryville, CA 94608 - Phone
- (510) 806-2549
Quick Facts
- NPI
- 1598394496
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 2
- Publications
- 20
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