A B Fulton
Overview
Explore the profile of A B Fulton including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
144
Citations
2578
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0
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Recent Articles
1.
Rubin L, Chan G, Barrett-Reis B, Fulton A, Hansen R, Ashmeade T, et al.
J Perinatol
. 2011 Jul;
32(6):418-24.
PMID: 21760585
Objective: Dietary carotenoids (lutein, lycopene and β-carotene) may be important in preventing or ameliorating prematurity complications. Little is known about carotenoid status or effects of supplementation. Study Design: This randomized...
2.
Marmor M, Fulton A, Holder G, Miyake Y, Brigell M, Bach M
Doc Ophthalmol
. 2008 Nov;
118(1):69-77.
PMID: 19030905
This document, from the International Society for Clinical Electrophysiology of Vision (ISCEV), presents an updated and revised ISCEV Standard for clinical electroretinography (ERG). The parameters for flash stimulation and background...
3.
Anselm I, Anselm I, Alkuraya F, Salomons G, Jakobs C, Fulton A, et al.
J Inherit Metab Dis
. 2006 Apr;
29(1):214-9.
PMID: 16601897
We report two unrelated boys with the X-linked creatine transporter defect (CRTR) and clinical features more severe than those previously described with this disorder. These two boys presented at ages...
4.
Rivolta C, Peck N, Fulton A, Fishman G, Berson E, Dryja T
Hum Mutat
. 2001 Dec;
18(6):550-1.
PMID: 11748859
Mutations in CRX, a photoreceptor-specific transcription factor, can cause Leber congenital amaurosis (LCA), cone-rod dystrophy (CORD), and retinitis pigmentosa (RP), all of which feature severe visual impairment. Upon screening 55...
5.
Mayer D, Hansen R, Moore B, Kim S, Fulton A
Arch Ophthalmol
. 2001 Nov;
119(11):1625-8.
PMID: 11709012
Objectives: To provide a description of refractive errors in healthy, term-born children, aged 1 through 48 months, and to test the hypotheses that spherical equivalent becomes significantly less hyperopic and...
6.
Fulton A, Hansen R, Petersen R, VanderVeen D
Arch Ophthalmol
. 2001 Apr;
119(4):499-505.
PMID: 11296015
Objective: To test the hypothesis that the more severe the acute phase retinopathy of prematurity (ROP) was in the preterm weeks, the more severely compromised is rod photoreceptor function after...
7.
Nishimura D, Searby C, Carmi R, Elbedour K, Van Maldergem L, Fulton A, et al.
Hum Mol Genet
. 2001 Apr;
10(8):865-74.
PMID: 11285252
Bardet-Biedl syndrome (BBS) is a genetically heterogeneous autosomal recessive disorder with the primary clinical features of obesity, pigmented retinopathy, polydactyly, hypogenitalism, mental retardation and renal anomalies. Associated features of the...
8.
Lotery A, Jacobson S, Fishman G, Weleber R, Fulton A, Namperumalsamy P, et al.
Arch Ophthalmol
. 2001 Mar;
119(3):415-20.
PMID: 11231775
Objectives: To test the hypothesis that mutations in the CRB1 gene cause Leber congenital amaurosis (LCA) and, if so, to describe the ocular phenotype of patients with LCA who harbor...
9.
Afshari M, Afshari N, Fulton A
Int Ophthalmol Clin
. 2001 Feb;
41(1):159-69.
PMID: 11198143
No abstract available.
10.
Hansen R, Fulton A
Invest Ophthalmol Vis Sci
. 2000 Nov;
41(13):4347-52.
PMID: 11095637
Purpose: To obtain and analyze scotopic increment threshold functions to test the hypothesis that rod photoreceptor immaturity accounts for the elevation of infants' over controls' dark-adapted thresholds and elevation of...