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HELEN MINTZ-HITTNER, M.D., F.A.C.S.
M.D., F.A.C.S.
Ophthalmology Physician
NPI: 1801993803Individual
Specialties, Licenses & Credentials
Ophthalmology PhysicianPrimary
Ophthalmology
Code: 207W00000X
D6034(TX)
Research & Publications (14)
Antivascular endothelial growth factor for retinopathy of prematurity.
PMID 19300261·Curr Opin Pediatr·2009
6-review
Intravitreal injection of bevacizumab (avastin) for treatment of stage 3 retinopathy of prematurity in zone I or posterior zone II.
PMID 18536599·Retina·2008
8-other
VSX1 (RINX) mutation with craniofacial anomalies, empty sella, corneal endothelial changes, and abnormal retinal and auditory bipolar cells.
PMID 15051220·Ophthalmology·2004
8-other
Successful amblyopia therapy initiated after age 7 years: compliance cures.
PMID 11074810·Arch Ophthalmol·2000
8-other
Intravitreous bevacizumab as anti-vascular endothelial growth factor therapy for retinopathy of prematurity: a morphologic study.
PMID 18695118·Arch Ophthalmol·2008
5-case
Further evidence of genetic heterogeneity in familial exudative vitreoretinopathy; exclusion of EVR1, EVR3, and EVR4 in a large autosomal dominant pedigree.
PMID 15665352·Br J Ophthalmol·2005
8-other
Laser in situ keratomileusis for treated anisometropic amblyopia in awake, autofixating pediatric and adolescent patients.
PMID 15617919·J Cataract Refract Surg·2004
8-other
Laser in situ keratomileusis for high hyperopia in awake, autofixating pediatric and adolescent patients with fully or partially accommodative esotropia.
PMID 15474825·J Cataract Refract Surg·2004
8-other
Traumatic optic nerve injury occurring after forceps delivery of a term newborn.
PMID 12736630·J AAPOS·2003
5-case
Microcornea and subluxated lenses due to a splicing error in the fibrillin-1 gene in a patient with Marfan syndrome.
PMID 12695261·Arch Ophthalmol·2003
5-case
Five novel RPGR mutations in families with X-linked retinitis pigmentosa.
PMID 11180598·Hum Mutat·2001
8-other
Mutations in the human forkhead transcription factor FOXE3 associated with anterior segment ocular dysgenesis and cataracts.
PMID 11159941·Hum Mol Genet·2001
7-preclinical
Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies.
PMID 11139241·Hum Mutat·2001
7-preclinical
Isolation and characterization of a novel human paired-like homeodomain-containing transcription factor gene, VSX1, expressed in ocular tissues.
PMID 10673340·Genomics·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
- 6400 FANNIN ST, SUITE 1800
HOUSTON, TX 77030 - Phone
- (713) 559-5200
Quick Facts
- NPI
- 1801993803
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 14
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