Anne B. Fulton, MD, divides her time equally between research and clinical practice. As Principal Investigator, she has had continuous NIH funding for more than 30 years. She and her laboratory group study the development of retinal and visual function in infants and children using molecular and structural approaches. She recognized the rod photoreceptors as a site of critical immaturity for infants’ vision and determined the growth curve for the rod visual pigment, rhodopsin, among other milestones, and she went on to show that rhodopsin content scales the developmental increment in dark-adapted retinal and visual sensitivity. She brought first-rate visual electrophysiology and visual psychophysics to our department, perfected the noninvasive assessments of infant and child patients, and related the normal developmental changes in retinal and visual function to the underlying biochemistry of the retina and retinal structure, including the seminal demonstration that the rhodopsin content of the retina scales retinal sensitivity in the developing human retina. More recently, she brought adaptive optics imaging to the department to provide non-invasive retinal assessments at a cellular level. Her currently funded research studies apply these procedures and concepts to the study of retinal disorders, including retinopathy of prematurity.
Research Background
Anne Fulton is a graduate of Tufts University School of Medicine. She completed an internship at Grady Memorial Hospital in Atlanta and a residency at Yale University School of Medicine.
Education
Undergraduate School
Radcliffe College
1962
Cambridge
MA
Medical School
Tufts University School of Medicine
1996
Boston
MA
Internship
Grady Memorial Hospital
1967
New Haven
CT
Residency
Yale University School of Medicine
1976
New Haven
CT
Media
Caregiver Profile
Meet Dr. Anne Fulton
Publications
Characterising the refractive error in paediatric patients with congenital stationary night blindness: a multicentre study. Br J Ophthalmol. 2025 Jan 28; 109(2):286-292. View Abstract
Advancing Insights into Pediatric Macular Diseases: A Comprehensive Review. J Clin Med. 2025 Jan 18; 14(2). View Abstract
Evaluating the Utility of Initial Exams in Retinopathy of Prematurity: Proposal of FIRST-ROP Algorithm for a Medium-Risk Cohort. Ophthalmology. 2025 Jan 08. View Abstract
HBS1L deficiency causes retinal dystrophy in a child and in a mouse model associated with defective development of photoreceptor cells. Dis Model Mech. 2024 Aug 01; 17(8). View Abstract
Validation of the "TWO-ROP" Algorithm at a Multi-Neonatal Intensive Care Unit Tertiary Referral Center. Ophthalmol Retina. 2025 Jan; 9(1):63-68. View Abstract
The Surviving, Not Thriving, Photoreceptors in Patients with ABCA4 Stargardt Disease. Diagnostics (Basel). 2024 Jul 17; 14(14). View Abstract
Refractive errors in patients with Bardet Biedl syndrome. Ophthalmic Genet. 2024 Oct; 45(5):435-440. View Abstract
Vision Loss and Difficulty Walking in a Pediatric Sexual Assault Victim. J Neuroophthalmol. 2024 Sep 01; 44(3):e498-e499. View Abstract
KEARNS-SAYRE SYNDROME MASQUERADING AS MYASTHENIA GRAVIS. Retin Cases Brief Rep. 2024 May 01; 18(3):396-399. View Abstract
Ciliopathy patient variants reveal organelle-specific functions for TUBB4B in axonemal microtubules. Science. 2024 Apr 26; 384(6694):eadf5489. View Abstract
Characteristics of Eyes With CRB1-Associated EOSRD/LCA: Age-Related Changes. Am J Ophthalmol. 2024 07; 263:168-178. View Abstract
Genetic deficiency of ribosomal rescue factor HBS1L causes retinal dystrophy associated with Pelota and EDF1 depletion. bioRxiv. 2023 Oct 20. View Abstract
A Simplified Model of Activation and Deactivation of Human Rod Phototransduction-An Electroretinographic Study. Invest Ophthalmol Vis Sci. 2023 09 01; 64(12):36. View Abstract
The Development of Retinal Function and Refractive Error in Children With Retinopathy of Prematurity. Invest Ophthalmol Vis Sci. 2023 08 01; 64(11):35. View Abstract
Do the retinal abnormalities in X-linked juvenile retinoschisis include impaired phototransduction? Exp Eye Res. 2023 09; 234:109591. View Abstract
Electroretinographic Responses in Retinopathy of Prematurity Treated Using Intravitreal Bevacizumab or Laser. Am J Ophthalmol. 2023 08; 252:275-285. View Abstract
Microcephaly and chorioretinopathy associated with TUBGCP4: a case report and a review of the literature. Ophthalmic Genet. 2023 Dec; 44(6):585-590. View Abstract
Modelling eye lengths and refractions in the periphery. Ophthalmic Physiol Opt. 2023 07; 43(4):815-826. View Abstract
Insights into the genotype-phenotype relationship of ocular manifestations in Kabuki syndrome. Am J Med Genet A. 2023 05; 191(5):1325-1338. View Abstract
Can Nerve Growth Factor (NGF) Be a Treatment Option for Pediatric Eye Diseases? Semin Ophthalmol. 2023 Jul; 38(5):427-432. View Abstract
The relation of the multifocal electroretinographic response to macular layer volume. Doc Ophthalmol. 2022 08; 145(1):1-10. View Abstract
Longitudinal Change of Refractive Error in Retinopathy of Prematurity Treated With Intravitreal Bevacizumab or Laser Photocoagulation. Am J Ophthalmol. 2022 08; 240:252-259. View Abstract
The Phenotypic and Mutational Spectrum of the FHONDA Syndrome and Oculocutaneous Albinism: Similarities and Differences. Invest Ophthalmol Vis Sci. 2022 01 03; 63(1):19. View Abstract
Evaluation of the Relationship Between Preferential Looking Testing and Visual Evoked Potentials as a Biomarker of Cerebral Visual Impairment. Front Hum Neurosci. 2021; 15:769259. View Abstract
Broadening INPP5E phenotypic spectrum: detection of rare variants in syndromic and non-syndromic IRD. NPJ Genom Med. 2021 Jun 29; 6(1):53. View Abstract
Fundus Pigmentary Whorls in a Patient With Mosaicism for Tetrasomy 3q. JAMA Ophthalmol. 2021 Jun 17. View Abstract
Cerebral visual impairment in CDKL5 deficiency disorder: vision as an outcome measure. Dev Med Child Neurol. 2021 11; 63(11):1308-1315. View Abstract
Artificial Intelligence (AI) Applications for Age-Related Macular Degeneration (AMD) and Other Retinal Dystrophies. Semin Ophthalmol. 2021 May 19; 36(4):304-309. View Abstract
Optical Coherence Tomography Angiography in Prematurity. Semin Ophthalmol. 2021 May 19; 36(4):264-269. View Abstract
Genetic causes of nystagmus, foveal hypoplasia and subnormal visual acuity- other than albinism. Ophthalmic Genet. 2021 06; 42(3):243-251. View Abstract
Dark-adapted threshold and electroretinogram for diagnosis of Usher syndrome. Doc Ophthalmol. 2021 08; 143(1):39-51. View Abstract
Homozygous deletion of 21q22.2 in a patient with hypotonia, developmental delay, cortical visual impairment, and retinopathy. Am J Med Genet A. 2021 02; 185(2):555-560. View Abstract
Carbonic anhydrase inhibition in X-linked retinoschisis: An eye on the photoreceptors. Exp Eye Res. 2021 01; 202:108344. View Abstract
The Fovea in Retinopathy of Prematurity. Invest Ophthalmol Vis Sci. 2020 09 01; 61(11):28. View Abstract
Retinal Function in X-Linked Juvenile Retinoschisis. Invest Ophthalmol Vis Sci. 2019 11 01; 60(14):4872-4881. View Abstract
Extracting the ON and OFF contributions to the full-field photopic flash electroretinogram using summed growth curves. Exp Eye Res. 2019 12; 189:107827. View Abstract
Impact of Obstructive Sleep Apnea on Optic Nerve Function in Patients With Craniosynostosis and Recurrent Intracranial Hypertension. Am J Ophthalmol. 2019 11; 207:356-362. View Abstract
Microperimetry in Three Inherited Retinal Disorders. Semin Ophthalmol. 2019; 34(4):334-339. View Abstract
The migraine eye: distinct rod-driven retinal pathways' response to dim light challenges the visual cortex hyperexcitability theory. Pain. 2019 Mar; 160(3):569-578. View Abstract
Neurobiology of Photophobia. J Neuroophthalmol. 2019 03; 39(1):94-102. View Abstract
High prevalence of strabismic visual field expansion in pediatric homonymous hemianopia. PLoS One. 2018; 13(12):e0209213. View Abstract
Color-selective photophobia in ictal vs interictal migraineurs and in healthy controls. Pain. 2018 Oct; 159(10):2030-2034. View Abstract
The importance of genetic testing as demonstrated by two cases of CACNA1F-associated retinal generation misdiagnosed as LCA. Mol Vis. 2017; 23:695-706. View Abstract
Increased Survival and Partly Preserved Cognition in a Patient With ACO2-Related Disease Secondary to a Novel Variant. J Child Neurol. 2017 08; 32(9):840-845. View Abstract
Multifocal ERG Responses in Subjects With a History of Preterm Birth. Invest Ophthalmol Vis Sci. 2017 05 01; 58(5):2603-2608. View Abstract
Progressive retinal degeneration in a girl with Knobloch syndrome who presented with signs of ocular albinism. Doc Ophthalmol. 2017 04; 134(2):135-140. View Abstract
Available Evidence on Leber Congenital Amaurosis and Gene Therapy. Semin Ophthalmol. 2017; 32(1):14-21. View Abstract
The neural retina in retinopathy of prematurity. Prog Retin Eye Res. 2017 01; 56:32-57. View Abstract
Reduced Left Lateralization of Language in Congenitally Blind Individuals. J Cogn Neurosci. 2017 Jan; 29(1):65-78. View Abstract
Retinal, visual, and refractive development in retinopathy of prematurity. Eye Brain. 2016; 8:103-111. View Abstract
Increment Threshold Functions in Retinopathy of Prematurity. Invest Ophthalmol Vis Sci. 2016 05 01; 57(6):2421-7. View Abstract
Expansion of phenotype and genotypic data in CRB2-related syndrome. Eur J Hum Genet. 2016 10; 24(10):1436-44. View Abstract
Differentiation of murine models of "negative ERG" by single and repetitive light stimuli. Doc Ophthalmol. 2016 Apr; 132(2):101-9. View Abstract
Extrafoveal Cone Packing in Eyes With a History of Retinopathy of Prematurity. Invest Ophthalmol Vis Sci. 2016 Feb; 57(2):467-75. View Abstract
Eye growth in term- and preterm-born eyes modeled from magnetic resonance images. Invest Ophthalmol Vis Sci. 2015 May; 56(5):3121-31. View Abstract
Vigabatrin can enhance electroretinographic responses in pigmented and albino rats. Doc Ophthalmol. 2015 Aug; 131(1):1-11. View Abstract
Temporal summation in children with a history of retinopathy of prematurity. Invest Ophthalmol Vis Sci. 2015 Jan 20; 56(2):914-7. View Abstract
Panel-based genetic diagnostic testing for inherited eye diseases is highly accurate and reproducible, and more sensitive for variant detection, than exome sequencing. Genet Med. 2015 Apr; 17(4):253-261. View Abstract
Effect of retinopathy of prematurity on scotopic spatial summation. Invest Ophthalmol Vis Sci. 2014 Apr 29; 55(5):3311-3. View Abstract
The rat with oxygen-induced retinopathy is myopic with low retinal dopamine. Invest Ophthalmol Vis Sci. 2013 Dec 19; 54(13):8275-84. View Abstract
The hermansky-pudlak syndrome: clinical features and imperatives from an ophthalmic perspective. Semin Ophthalmol. 2013 Sep-Nov; 28(5-6):387-91. View Abstract
CRB1: one gene, many phenotypes. Semin Ophthalmol. 2013 Sep-Nov; 28(5-6):397-405. View Abstract
Introduction to the special issue: vision after premature birth. Doc Ophthalmol. 2013 Aug; 127(1):1-2. View Abstract
Photoreceptor and postreceptor responses in congenital stationary night blindness. Invest Ophthalmol Vis Sci. 2013 Jul 10; 54(7):4648-58. View Abstract
Next-generation sequencing analysis of gene regulation in the rat model of retinopathy of prematurity. Doc Ophthalmol. 2013 Aug; 127(1):13-31. View Abstract
Alterations of the tunica vasculosa lentis in the rat model of retinopathy of prematurity. Doc Ophthalmol. 2013 Aug; 127(1):3-11. View Abstract
Multimodal adaptive optics retinal imager: design and performance. J Opt Soc Am A Opt Image Sci Vis. 2012 Dec 01; 29(12):2598-607. View Abstract
Electroretinographic (ERG) responses in pediatric patients using vigabatrin. Doc Ophthalmol. 2012 Jun; 124(3):197-209. View Abstract
Effect of carotenoid supplementation on plasma carotenoids, inflammation and visual development in preterm infants. J Perinatol. 2012 Jun; 32(6):418-24. View Abstract
Variations in NPHP5 in patients with nonsyndromic leber congenital amaurosis and Senior-Loken syndrome. Arch Ophthalmol. 2011 Jan; 129(1):81-7. View Abstract
Long-term effects of retinopathy of prematurity (ROP) on rod and rod-driven function. Doc Ophthalmol. 2011 Feb; 122(1):19-27. View Abstract
Cone ERG responses in patients with Smith-Lemli-Opitz Syndrome (SLOS). Doc Ophthalmol. 2010 Oct; 121(2):85-91. View Abstract
The cone electroretinogram in retinopathy of prematurity. Invest Ophthalmol Vis Sci. 2008 Feb; 49(2):814-9. View Abstract
Foveal fine structure in retinopathy of prematurity: an adaptive optics Fourier domain optical coherence tomography study. Invest Ophthalmol Vis Sci. 2008 May; 49(5):2061-70. View Abstract
The oscillatory potentials of the dark-adapted electroretinogram in retinopathy of prematurity. Invest Ophthalmol Vis Sci. 2007 Dec; 48(12):5788-97. View Abstract
Effects of desferoxamine on retinal and visual function. Arch Ophthalmol. 2007 Nov; 125(11):1581-2. View Abstract
Development of scotopic visual thresholds in retinopathy of prematurity. Invest Ophthalmol Vis Sci. 2007 Oct; 48(10):4854-60. View Abstract
The genetics and ocular findings of Alagille syndrome. Semin Ophthalmol. 2007 Oct-Dec; 22(4):205-10. View Abstract
Rod photoreceptor function predicts blood vessel abnormality in retinopathy of prematurity. Invest Ophthalmol Vis Sci. 2007 Sep; 48(9):4351-9. View Abstract
Retinal degeneration in children: dark adapted visual threshold and arteriolar diameter. Vision Res. 2008 Feb; 48(3):325-31. View Abstract
Development of the electroretinographic oscillatory potentials in normal and ROP rats. Invest Ophthalmol Vis Sci. 2006 Dec; 47(12):5447-52. View Abstract
Pediatric clinical visual electrophysiology: a survey of actual practice. Doc Ophthalmol. 2006 Nov; 113(3):193-204. View Abstract
The retinal vasculature and function of the neural retina in a rat model of retinopathy of prematurity. Invest Ophthalmol Vis Sci. 2006 Jun; 47(6):2639-47. View Abstract
Proceedings of the Third International Symposium on Retinopathy of Prematurity: an update on ROP from the lab to the nursery (November 2003, Anaheim, California). Mol Vis. 2006 May 23; 12:532-80. View Abstract
Multifocal ERG in subjects with a history of retinopathy of prematurity. Doc Ophthalmol. 2005 Jul; 111(1):7-13. View Abstract
X-linked creatine transporter defect: a report on two unrelated boys with a severe clinical phenotype. J Inherit Metab Dis. 2006 Feb; 29(1):214-9. View Abstract
Diagnosis of plus disease in retinopathy of prematurity using Retinal Image multiScale Analysis. Invest Ophthalmol Vis Sci. 2005 Dec; 46(12):4734-8. View Abstract
Development of the cone ERG in infants. Invest Ophthalmol Vis Sci. 2005 Sep; 46(9):3458-62. View Abstract
Development of visual acuity in children with cerebral visual impairment. Arch Ophthalmol. 2005 Sep; 123(9):1215-20. View Abstract
Maculopathy and retinal degeneration in cobalamin C methylmalonic aciduria and homocystinuria. Arch Ophthalmol. 2005 Aug; 123(8):1143-6. View Abstract
Early ametropia and rod photoreceptor function in retinopathy of prematurity. Optom Vis Sci. 2005 Apr; 82(4):307-17. View Abstract
Recovery of the rod photoresponse in infants. Invest Ophthalmol Vis Sci. 2005 Feb; 46(2):764-8. View Abstract
Comparison of ERGs recorded with skin and corneal-contact electrodes in normal children and adults. Doc Ophthalmol. 2004 Jul; 109(1):43-55. View Abstract
Recovery of the rod photoresponse in infant rats. Vision Res. 2003 Dec; 43(28):3081-5. View Abstract
Rod photoreceptor responses in children with Smith-Lemli-Opitz syndrome. Arch Ophthalmol. 2003 Dec; 121(12):1738-43. View Abstract
Development of ERG responses: the ISCEV rod, maximal and cone responses in normal subjects. Doc Ophthalmol. 2003 Nov; 107(3):235-41. View Abstract
Effects of telazol and nembutal on retinal responses. Doc Ophthalmol. 2003 Jul; 107(1):45-51. View Abstract
Retinal function in carriers of Bardet-Biedl syndrome. Arch Ophthalmol. 2003 Jun; 121(6):804-10. View Abstract
Evaluation of complex inheritance involving the most common Bardet-Biedl syndrome locus (BBS1). Am J Hum Genet. 2003 Feb; 72(2):429-37. View Abstract
Rod photoreceptor function in children with mitochondrial disorders. Arch Ophthalmol. 2002 Aug; 120(8):1055-62. View Abstract
Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome. Nat Genet. 2002 Aug; 31(4):435-8. View Abstract
Fundus photography for measurement of macular pigment density distribution in children. Invest Ophthalmol Vis Sci. 2002 May; 43(5):1450-5. View Abstract
Background adaptation in a rat model of retinopathy of prematurity. Doc Ophthalmol. 2002 Jan; 104(1):97-105. View Abstract
Novel frameshift mutations in CRX associated with Leber congenital amaurosis. Hum Mutat. 2001 Dec; 18(6):550-1. View Abstract
Cycloplegic refractions in healthy children aged 1 through 48 months. Arch Ophthalmol. 2001 Nov; 119(11):1625-8. View Abstract
Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2). Hum Mol Genet. 2001 Apr 01; 10(8):865-74. View Abstract
The rod photoreceptors in retinopathy of prematurity: an electroretinographic study. Arch Ophthalmol. 2001 Apr; 119(4):499-505. View Abstract
Mutations in the CRB1 gene cause Leber congenital amaurosis. Arch Ophthalmol. 2001 Mar; 119(3):415-20. View Abstract
Cortical visual impairment in infants and children. Int Ophthalmol Clin. 2001; 41(1):159-69. View Abstract
Rod-mediated increment threshold functions in infants. Invest Ophthalmol Vis Sci. 2000 Dec; 41(13):4347-52. View Abstract
The development of scotopic sensitivity. Invest Ophthalmol Vis Sci. 2000 May; 41(6):1588-96. View Abstract
Background adaptation in children with a history of mild retinopathy of prematurity. Invest Ophthalmol Vis Sci. 2000 Jan; 41(1):320-4. View Abstract
The rhodopsin content of human eyes. Invest Ophthalmol Vis Sci. 1999 Jul; 40(8):1878-83. View Abstract
The course of maturation of rod-mediated visual thresholds in infants. Invest Ophthalmol Vis Sci. 1999 Jul; 40(8):1883-6. View Abstract
Rod photoreceptor maturation does not vary with retinal eccentricity in mammalian retina. Curr Eye Res. 1999 Jun; 18(6):393-402. View Abstract
Genetic defects and clinical characteristics of patients with a form of oculocutaneous albinism (Hermansky-Pudlak syndrome) [correction of (Hennansky-Pudlak)]. Arch Ophthalmol. 1999 Feb; 117(2):251-2. View Abstract
Rod photoreceptors in infant rats with a history of oxygen exposure. Invest Ophthalmol Vis Sci. 1999 Jan; 40(1):168-74. View Abstract
Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis. Proc Natl Acad Sci U S A. 1998 Mar 17; 95(6):3088-93. View Abstract
Rod and rod mediated function in patients with beta-thalassemia major. Doc Ophthalmol. 1998-1999; 96(4):333-45. View Abstract
Central retinal vein occlusion in a young child with cyanotic heart disease. Arch Ophthalmol. 1997 Aug; 115(8):1077. View Abstract
Dark-adapted thresholds in children with histories of mild retinopathy of prematurity. Invest Ophthalmol Vis Sci. 1997 May; 38(6):1175-83. View Abstract
Rhodopsin in immature rod outer segments. Invest Ophthalmol Vis Sci. 1996 Sep; 37(10):1951-6. View Abstract
Photoreceptor function in infants and children with a history of mild retinopathy of prematurity. J Opt Soc Am A Opt Image Sci Vis. 1996 Mar; 13(3):566-71. View Abstract
Effect of prior oxygen exposure on the electroretinographic responses of infant rats. Invest Ophthalmol Vis Sci. 1995 Sep; 36(10):2071-9. View Abstract
The effects of acetazolamide on the electroretinographic responses in rats. Invest Ophthalmol Vis Sci. 1995 May; 36(6):1019-26. View Abstract
The development of the rod photoresponse from dark-adapted rats. Invest Ophthalmol Vis Sci. 1995 May; 36(6):1038-45. View Abstract
The course of myopia in children with mild retinopathy of prematurity. Vision Res. 1995 May; 35(9):1329-35. View Abstract
Dark-adapted thresholds at 10- and 30-deg eccentricities in 10-week-old infants. Vis Neurosci. 1995 May-Jun; 12(3):509-12. View Abstract
The VEP thresholds for full-field stimuli in dark-adapted infants. Vis Neurosci. 1995 Mar-Apr; 12(2):223-8. View Abstract
Electroretinogram responses and refractive errors in patients with a history of retinopathy prematurity. Doc Ophthalmol. 1995-1996; 91(2):87-100. View Abstract
Scotopic optokinetic nystagmus thresholds in 10-week-old infants. Invest Ophthalmol Vis Sci. 1994 Mar; 35(3):1246-9. View Abstract
Scotopic center surround organization in 10-week-old infants. Vision Res. 1994 Mar; 34(5):621-4. View Abstract
Foveal cone pigments and sensitivity in young patients with Usher's syndrome. Am J Ophthalmol. 1987 Feb 15; 103(2):150-60. View Abstract
Intramuscular vitamin E repletion in children with chronic cholestasis. Am J Dis Child. 1987 Feb; 141(2):170-4. View Abstract
Concurrence of congenital ocular motor apraxia and other motor problems: an expanded syndrome. Dev Med Child Neurol. 1987 Feb; 29(1):85-90. View Abstract
The relationship of retinal sensitivity and rhodopsin in human infants. Vision Res. 1987; 27(5):697-704. View Abstract
"Self-screening" of rhodopsin in rod outer segments. Vision Res. 1987; 27(9):1459-70. View Abstract
Pupillary changes during dark adaptation in human infants. Invest Ophthalmol Vis Sci. 1986 Dec; 27(12):1726-9. View Abstract
Assessment of acuity of amblyopic subjects using face, grating, and recognition stimuli. Invest Ophthalmol Vis Sci. 1986 Jul; 27(7):1184-7. View Abstract
Background adaptation in human infants. Vision Res. 1986; 26(5):771-9. View Abstract
Electroretinography: application to clinical studies of infants. J Pediatr Ophthalmol Strabismus. 1985 Nov-Dec; 22(6):251-5. View Abstract
Assessment of young amblyopes. Array vs. single picture acuities. Ophthalmology. 1985 Sep; 92(9):1197-202. View Abstract
Retinal degenerations and brain abnormalities in infants and young children. Doc Ophthalmol. 1985 Aug 30; 60(2):133-40. View Abstract
Visual acuity of infants and children with retinal degenerations. Ophthalmic Paediatr Genet. 1985 Feb; 5(1-2):51-6. View Abstract
Preferential looking grating acuities of infants at risk of amblyopia. Trans Ophthalmol Soc U K (1962). 1985; 104 ( Pt 8):903-11. View Abstract
Grating and recognition acuities of pediatric patients. Ophthalmology. 1984 Aug; 91(8):947-53. View Abstract
Assessment of acuity in human infants using face and grating stimuli. Invest Ophthalmol Vis Sci. 1984 Jul; 25(7):782-6. View Abstract
The relation of retinal sensitivity and rhodopsin in developing rat retina. Invest Ophthalmol Vis Sci. 1984 Jun; 25(6):647-51. View Abstract
Retinal degeneration in vitamin B12 disorder associated with methylmalonic aciduria and sulfur amino acid abnormalities. Am J Ophthalmol. 1984 Jun; 97(6):691-6. View Abstract
Cycloplegic refractions of infants and young children: the axis of astigmatism. Invest Ophthalmol Vis Sci. 1984 Jan; 25(1):83-7. View Abstract
Retinal sensitivity and adaptation in pediatric patients. Behav Brain Res. 1983 Oct; 10(1):59-70. View Abstract
Preferential looking acuity of pediatric patients with developmental disabilities. Behav Brain Res. 1983 Oct; 10(1):189-97. View Abstract
Background adaptation in RCS rats. Invest Ophthalmol Vis Sci. 1983 Jan; 24(1):72-6. View Abstract
Preferential looking vision testing: application to evaluation of high-risk, prematurely born infants and children. J Pediatr Ophthalmol Strabismus. 1982 Nov-Dec; 19(6):286-93. View Abstract
Preferential looking acuity obtained with a staircase procedure in pediatric patients. Invest Ophthalmol Vis Sci. 1982 Oct; 23(4):538-43. View Abstract
Scotopic thresholds and plasma retinol in cystic fibrosis. Invest Ophthalmol Vis Sci. 1982 Sep; 23(3):364-70. View Abstract
The relation of myopia and astigmatism in developing eyes. Ophthalmology. 1982 Apr; 89(4):298-302. View Abstract
Dark-adapted sensitivity, rhodopsin content, and background adaptation in pcd/pcd mice. Invest Ophthalmol Vis Sci. 1982 Mar; 22(3):386-93. View Abstract
Development of the outer plexiform layer in albino rats. Curr Eye Res. 1982-1983; 2(5):295-9. View Abstract
Retinal degeneration in the delayed amelanotic (DAM) chicken: an electroretinographic study. Curr Eye Res. 1982-1983; 2(11):757-63. View Abstract
Behavioral measurement of background adaptation in infants. Invest Ophthalmol Vis Sci. 1981 Oct; 21(4):625-9. View Abstract
Cycloplegic refractions of premature infants. Am J Ophthalmol. 1981 Apr; 91(4):490-5. View Abstract
Cone pigments in acute posterior multifocal placoid pigment epitheliopathy. Am J Ophthalmol. 1981 Apr; 91(4):465-8. View Abstract
Cycloplegic refractions in infants and young children. Am J Ophthalmol. 1980 Aug; 90(2):239-47. View Abstract
Increased incidence of choroidal malignant melanoma occurring in a single population of chemical workers. Am J Ophthalmol. 1980 Mar; 89(3):323-37. View Abstract
Background adaptation in developing rat retina: an electroretinographic study. Vision Res. 1980; 20(10):819-26. View Abstract
Retinal anomalies in trisomy 18. Albrecht Von Graefes Arch Klin Exp Ophthalmol. 1980; 213(3):195-205. View Abstract
Epidemikological investigation of increased incidence of choroidal melanoma in a single population of chemical workers. Int Ophthalmol Clin. 1980; 20(2):71-92. View Abstract
Infant vision testing by a behavioral method. Ophthalmology. 1979 Mar; 86(3):431-9. View Abstract
A behavioral method for efficient screening of visual acuity in young infants. II. Clinical application. Invest Ophthalmol Vis Sci. 1978 Dec; 17(12):1151-7. View Abstract
Human retinal dysplasia. Am J Ophthalmol. 1978 May; 85(5 Pt 1):690-8. View Abstract
Human albinism. Light and electron microscopy study. Arch Ophthalmol. 1978 Feb; 96(2):305-10. View Abstract
Rod ERG of the mudpuppy: effect of dim red backgrounds. Vision Res. 1978; 18(7):785-92. View Abstract
The human rod ERG: correlation with psychophysical responses in light and dark adaptation. Vision Res. 1978; 18(7):793-800. View Abstract
Ocular findings in triploidy. Am J Ophthalmol. 1977 Dec; 84(6):859-67. View Abstract
Spontaneous anophthalmia and microphthalmia in white-tailed deer. J Comp Pathol. 1977 Oct; 87(4):557-68. View Abstract
Active giant cell arteritis with cerebral involvement. Findings following four years of corticosteroid therapy. Arch Ophthalmol. 1976 Dec; 94(12):2068-71. View Abstract
Gastrointestinal sarcoidosis diagnosed by conjunctival biopsy. Am J Ophthalmol. 1976 Jul; 82(1):102-4. View Abstract
Dark adaptation and the rate of pigment regeneration. Vision Res. 1969 Dec; 9(12):1473-9. View Abstract
Dark adaptation: free opsin or regeneration rate? J Physiol. 1969 Oct; 204(2):124P+. View Abstract