Helen Mintz-Hittner
Helen Mintz-Hittner
Professor of Ophthalmology and Visual Science, University of Texas Houston Medical School
Verified email at uth.tmc.edu
TitleCited byYear
Efficacy of intravitreal bevacizumab for stage 3+ retinopathy of prematurity
HA Mintz-Hittner, KA Kennedy, AZ Chuang
New England Journal of Medicine 364 (7), 603-615, 2011
9702011
A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD
EV Semina, RE Ferrell, HA Mintz-Hittner, P Bitoun, WLM Alward, ...
Nature genetics 19 (2), 167-170, 1998
3831998
A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor gene
MM Sohocki, LS Sullivan, HA Mintz-Hittner, D Birch, JR Heckenlively, ...
The American Journal of Human Genetics 63 (5), 1307-1315, 1998
2891998
Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies
MM Sohocki, SP Daiger, SJ Bowne, JA Rodriquez, H Northrup, ...
Human mutation 17 (1), 42-51, 2001
2852001
Intravitreal injection of bevacizumab (avastin) for treatment of stage 3 retinopathy of prematurity in zone I or posterior zone II
HA Mintz-Hittner, JR RONALD R KUFFEL
Retina 28 (6), 831-838, 2008
2582008
Mutations in the human forkhead transcription factor FOXE3 associated with anterior segment ocular dysgenesis and cataracts
EV Semina, I Brownell, HA Mintz-Hittner, JC Murray, M Jamrich
Human molecular genetics 10 (3), 231-236, 2001
1992001
Successful amblyopia therapy initiated after age 7 years: compliance cures
HA Mintz-Hittner, KM Fernandez
Archives of ophthalmology 118 (11), 1535-1541, 2000
1492000
Refractive outcomes following bevacizumab monotherapy compared with conventional laser treatment: a randomized clinical trial
MM Geloneck, AZ Chuang, WL Clark, MG Hunt, AA Norman, ...
JAMA ophthalmology 132 (11), 1327-1333, 2014
1392014
Intravitreous bevacizumab as anti–vascular endothelial growth factor therapy for retinopathy of prematurity: a morphologic study
L Kong, HA Mintz-Hittner, RL Penland, FL Kretzer, P Chévez-Barrios
Archives of Ophthalmology 126 (8), 1161-1163, 2008
1092008
Antivascular endothelial growth factor for retinopathy of prematurity
HA Mintz-Hittner, LM Best
Current opinion in pediatrics 21 (2), 182-187, 2009
902009
Isolation and characterization of a novel human paired-like homeodomain-containing transcription factor gene, VSX1, expressed in ocular tissues
EV Semina, HA Mintz-Hittner, JC Murray
Genomics 63 (2), 289-293, 2000
872000
A small foveal avascular zone may be an historic mark of prematurity
HA Mintz-Hittner, DM Knight-Nanan, DR Satriano, FL Kretzer
Ophthalmology 106 (7), 1409-1413, 1999
791999
Paired box mutations in familial and sporadic aniridia predicts truncated aniridia proteins.
A Martha, RE Ferrell, H Mintz-Hittner, LA Lyons, GF Saunders
American journal of human genetics 54 (5), 801, 1994
781994
Beat-ROP Cooperative Group
HA Mintz-Hittner, KA Kennedy, AZ Chuang
Efficacy of intravitreal bevacizumab for stage 3, 603-615, 2011
762011
Clinical management of recurrent retinopathy of prematurity after intravitreal bevacizumab monotherapy
HA Mintz-Hittner, MM Geloneck, AZ Chuang
Ophthalmology 123 (9), 1845-1855, 2016
732016
Treatment of retinopathy of prematurity with vascular endothelial growth factor inhibitors
HA Mintz-Hittner
Early human development 88 (12), 937-941, 2012
672012
Recessive mutations in TSPAN12 cause retinal dysplasia and severe familial exudative vitreoretinopathy (FEVR)
JA Poulter, AE Davidson, M Ali, DF Gilmour, DA Parry, HA Mintz-Hittner, ...
Investigative ophthalmology & visual science 53 (6), 2873-2879, 2012
652012
Laser in situ keratomileusis for treated anisometropic amblyopia in awake, autofixating pediatric and adolescent patients
CB Phillips, TC Prager, G McClellan, HA Mintz-Hittner
Journal of Cataract & Refractive Surgery 30 (12), 2522-2528, 2004
532004
VSX1 (RINX) mutation with craniofacial anomalies, empty sella, corneal endothelial changes, and abnormal retinal and auditory bipolar cells
HA Mintz-Hittner, EV Semina, LJ Frishman, TC Prager, JC Murray
Ophthalmology 111 (4), 828-836, 2004
472004
Resolution of the two loci for autosomal dominant aniridia, AN1 and AN2, to a single locus on chromosome 11p13
LA Lyons, A Martha, HA Mintz-Hittner, GF Saunders, RE Ferrell
Genomics 13 (4), 925-930, 1992
451992
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