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EKATERINI TSILOU, M.D.
M.D.
Ophthalmology Physician
NPI: 1598093908Individual
Specialties, Licenses & Credentials
Ophthalmology PhysicianPrimary
Ophthalmology
Code: 207W00000X
MD31284(DC)
Research & Publications (20)
Nephropathic cystinosis: posterior segment manifestations and effects of cysteamine therapy.
PMID 16603246·Ophthalmology·2006
8-other
Eyelid myxoma in Carney complex without PRKAR1A allelic loss.
PMID 15368482·Am J Med Genet A·2004
5-case
Milder ocular findings in Hermansky-Pudlak syndrome type 3 compared with Hermansky-Pudlak syndrome type 1.
PMID 15288994·Ophthalmology·2004
4-observational
Bilateral late posterior chamber intraocular lens dislocation with the capsular bag in a patient with gyrate atrophy.
PMID 15210246·J Cataract Refract Surg·2004
5-case
A multicentre randomised double masked clinical trial of a new formulation of topical cysteamine for the treatment of corneal cystine crystals in cystinosis.
PMID 12488257·Br J Ophthalmol·2003
3-trial
Retinal visualization in an eye with corneal crystals using indocyanine green videoangiography.
PMID 12095822·Am J Ophthalmol·2002
5-case
Usher syndrome clinical types I and II: could ocular symptoms and signs differentiate between the two types?
PMID 11952489·Acta Ophthalmol Scand·2002
8-other
Age-related prevalence of anterior segment complications in patients with infantile nephropathic cystinosis.
PMID 11862089·Cornea·2002
8-other
MKS3-related ciliopathy with features of autosomal recessive polycystic kidney disease, nephronophthisis, and Joubert Syndrome.
PMID 19540516·J Pediatr·2009
5-case
Dyskeratosis congenita: the first NIH clinical research workshop.
PMID 19415736·Pediatr Blood Cancer·2009
8-other
Hermansky-Pudlak syndrome type 1 in patients of Indian descent.
PMID 19398212·Mol Genet Metab·2009
5-case
Hermansky-Pudlak syndrome in two African-American brothers.
PMID 19334085·Am J Med Genet A·2009
5-case
Mutation spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual function.
PMID 18181211·Hum Mutat·2008
7-preclinical
Cellular defects in Chediak-Higashi syndrome correlate with the molecular genotype and clinical phenotype.
PMID 17554367·J Invest Dermatol·2007
5-case
Ocular pathologic features of Hermansky-Pudlak syndrome type 1 in an adult.
PMID 16832032·Arch Ophthalmol·2006
5-case
Rieger's anomaly and other ocular abnormalities in association with osteogenesis imperfecta and a COL1A1 mutation.
PMID 16272059·Ophthalmic Genet·2005
5-case
Stickler syndrome: clinical characteristics and diagnostic criteria.
PMID 16152640·Am J Med Genet A·2005
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
- NEI NIH 10 CENTER DR BLDG 10, RM 10N226
BETHESDA, MD 20892 - Phone
- (301) 402-2391
Quick Facts
- NPI
- 1598093908
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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