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ELIAS TRABOULSI, MD
MD
Ophthalmology Physician
NPI: 1669414132IndividualAccepts Medicare
Specialties, Licenses & Credentials
Ophthalmology PhysicianPrimary
Ophthalmology
Code: 207W00000X
35072624(OH)
CMS Specialties
PrimaryOPHTHALMOLOGY
Education
OTHER
Class of 1982
Research & Publications (20)
Aniridia with preserved visual function: a report of four cases with no mutations in PAX6.
PMID 18243151·Am J Ophthalmol·2008
5-case
Vision First, a program to detect and treat eye diseases in young children: the first four years.
PMID 19277233·Trans Am Ophthalmol Soc·2008
8-other
Ocular manifestations of familial adenomatous polyposis (Gardner syndrome).
PMID 15763201·Ophthalmol Clin North Am·2005
8-other
Polychromasia capsulare (multicolored capsule): report of three families.
PMID 17057792·Trans Am Ophthalmol Soc·2005
5-case
Ocular findings in ichthyosis follicularis-alopecia-photophobia (IFAP) syndrome.
PMID 15370546·Ophthalmic Genet·2004
5-case
Congenital abnormalities of cranial nerve development: overview, molecular mechanisms, and further evidence of heterogeneity and complexity of syndromes with congenital limitation of eye movements.
PMID 15747768·Trans Am Ophthalmol Soc·2004
5-case
Microfibril abnormalities of the lens capsule in patients with Marfan syndrome and ectopia lentis.
PMID 10779844·Ophthalmic Genet·2000
8-other
Evidence of genetic heterogeneity in autosomal recessive congenital fibrosis of the extraocular muscles.
PMID 10844060·Am J Ophthalmol·2000
8-other
Coats' disease, megalopapilla and Cornelia de Lange syndrome.
PMID 19373684·Ophthalmic Genet·2009
5-case
Sequence alterations in RX in patients with microphthalmia, anophthalmia, and coloboma.
PMID 19158959·Mol Vis·2009
8-other
Novel ABCA4 compound heterozygous mutations cause severe progressive autosomal recessive cone-rod dystrophy presenting as Stargardt disease.
PMID 19352439·Mol Vis·2009
5-case
The value of keratometry and central corneal thickness measurements in the clinical diagnosis of Marfan syndrome.
PMID 18378212·Am J Ophthalmol·2008
4-observational
Descemet stripping automated endothelial keratoplasty in a 2-year-old child.
PMID 18589389·J AAPOS·2008
5-case
Functional analysis of an ADAMTS10 signal peptide mutation in Weill-Marchesani syndrome demonstrates a long-range effect on secretion of the full-length enzyme.
PMID 18567016·Hum Mutat·2008
7-preclinical
Giant intracavernous carotid aneurysm presenting as isolated sixth nerve palsy in an infant.
PMID 18369076·Br J Ophthalmol·2008
5-case
CNGA3 mutations in two United Arab Emirates families with achromatopsia.
PMID 18636117·Mol Vis·2008
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
- 9500 EUCLID AVE
CLEVELAND, OH 44195 - Phone
- (800) 223-2273
Quick Facts
- NPI
- 1669414132
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 44
- Publications
- 20
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