Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1983 1
1990 1
1999 1
2000 1
2005 1
2009 1
2011 1
2012 3
2015 1
2018 1
2020 1
2022 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

13 results

Results by year

Filters applied: . Clear all
Quoted phrase not found in phrase index: "Abnormal kinetic perimetry test"
Page 1
Natural history of Usher type 2 with the c.2299delG mutation of USH2A in a large cohort.
Meunier A, Zanlonghi X, Roux AF, Fils JF, Caspers L, Migeotte I, Abramowicz M, Meunier I. Meunier A, et al. Ophthalmic Genet. 2022 Aug;43(4):470-475. doi: 10.1080/13816810.2022.2051191. Epub 2022 Mar 28. Ophthalmic Genet. 2022. PMID: 35345973
MATERIALS AND METHODS: We compared the ocular and auditory phenotypes in a retrospective cohort of 169 Usher type 2 patients, with and without the c.2299delG allele, including visual acuity, slit-lamp examination, optical coherence tomography, kinetic perimetry …
MATERIALS AND METHODS: We compared the ocular and auditory phenotypes in a retrospective cohort of 169 Usher type 2 patients, with and witho …
Clinical and electroretinographic findings of female carriers and affected males in a progressive X-linked cone-rod dystrophy (COD-1) pedigree.
Brown J Jr, Kimura AE, Gorin MB. Brown J Jr, et al. Ophthalmology. 2000 Jun;107(6):1104-10. doi: 10.1016/s0161-6420(00)00086-5. Ophthalmology. 2000. PMID: 10857830
METHODS: A history of visual impairment including age at onset, loss of acuity, color vision abnormalities, photophobia, and nyctalopia was obtained. A complete ophthalmologic examination was performed, including kinetic perimetry with a Goldmann perim …
METHODS: A history of visual impairment including age at onset, loss of acuity, color vision abnormalities, photophobia, and n …
Efficacy Outcome Measures for Clinical Trials of USH2A Caused by the Common c.2299delG Mutation.
Calzetti G, Levy RA, Cideciyan AV, Garafalo AV, Roman AJ, Sumaroka A, Charng J, Heon E, Jacobson SG. Calzetti G, et al. Am J Ophthalmol. 2018 Sep;193:114-129. doi: 10.1016/j.ajo.2018.06.017. Epub 2018 Jun 25. Am J Ophthalmol. 2018. PMID: 29953849
PURPOSE: To determine the change in vision and retinal structure in patients with the common c.2299delG mutation in the USH2A gene in anticipation of clinical trials of therapy. DESIGN: Retrospective observational case series. METHODS: Eighteen patients, homozygotes …
PURPOSE: To determine the change in vision and retinal structure in patients with the common c.2299delG mutation in the USH2A gene in antici …
Autosomal Dominant Retinal Dystrophy With Electronegative Waveform Associated With a Novel RAX2 Mutation.
Yang P, Chiang PW, Weleber RG, Pennesi ME. Yang P, et al. JAMA Ophthalmol. 2015 Jun;133(6):653-61. doi: 10.1001/jamaophthalmol.2015.0357. JAMA Ophthalmol. 2015. PMID: 25789692 Free PMC article.
OBJECTIVES: To clinically evaluate 4 patients and 5 unaffected family members, characterize the disease phenotype over time, and identify the associated genetic mutation. DESIGN, SETTING, AND PARTICIPANTS: A prospective, longitudinal, observational, case-series anal …
OBJECTIVES: To clinically evaluate 4 patients and 5 unaffected family members, characterize the disease phenotype over time, and identify th …
Visual function in epilepsy patients treated with initial valproate monotherapy.
Sorri I, Rissanen E, Mäntyjärvi M, Kälviäinen R. Sorri I, et al. Seizure. 2005 Sep;14(6):367-70. doi: 10.1016/j.seizure.2005.04.010. Seizure. 2005. PMID: 15939631 Free article. Clinical Trial.
RESULTS: None had vigabatrin-type, concentric visual field defect with the kinetic Goldmann or automated Humphrey perimetries. ...CONCLUSIONS: The use of VPA in the treatment of epilepsy is not associated with visual field defects similar …
RESULTS: None had vigabatrin-type, concentric visual field defect with the kinetic Goldmann or automated Humphrey pe …
Retinal function in Stargardt's disease and fundus flavimaculatus.
Moloney JB, Mooney DJ, O'Connor MA. Moloney JB, et al. Am J Ophthalmol. 1983 Jul;96(1):57-65. doi: 10.1016/0002-9394(83)90455-5. Am J Ophthalmol. 1983. PMID: 6869480
Visual acuity and color discrimination were reduced in all patients (mean visual acuity, 20/120; mean error score, 365). On electroretinography all patients had some significant abnormality of cone function and 24 eyes had abnormal rod function …
Visual acuity and color discrimination were reduced in all patients (mean visual acuity, 20/120; mean error score, 365) …
Baseline Visual Field Findings in the RUSH2A Study: Associated Factors and Correlation With Other Measures of Disease Severity.
Duncan JL, Liang W, Maguire MG, Audo I, Ayala AR, Birch DG, Carroll J, Cheetham JK, Esposti SD, Durham TA, Erker L, Farsiu S, Ferris FL 3rd, Heon E, Hufnagel RB, Iannaccone A, Jaffe GJ, Kay CN, Michaelides M, Pennesi ME, Sahel JA; Foundation Fighting Blindness Consortium Investigator Group. Duncan JL, et al. Am J Ophthalmol. 2020 Nov;219:87-100. doi: 10.1016/j.ajo.2020.05.024. Epub 2020 May 22. Am J Ophthalmol. 2020. PMID: 32446738 Free PMC article.
STUDY POPULATION: Usher syndrome type 2 (USH2) (n = 80) or autosomal recessive nonsyndromic retinitis pigmentosa (ARRP) (n = 47) associated with biallelic disease-causing sequence variants in USH2A. OBSERVATION PROCEDURES: Repeatability of full-field static perim …
STUDY POPULATION: Usher syndrome type 2 (USH2) (n = 80) or autosomal recessive nonsyndromic retinitis pigmentosa (ARRP) (n = 47) associated …
Comparison of central and peripheral visual field properties in the optic neuritis treatment trial.
Keltner JL, Johnson CA, Spurr JO, Beck RW. Keltner JL, et al. Am J Ophthalmol. 1999 Nov;128(5):543-53. doi: 10.1016/s0002-9394(99)00304-9. Am J Ophthalmol. 1999. PMID: 10577521 Clinical Trial.
PURPOSE: To compare the results of peripheral kinetic visual field testing and central static perimetry for patients enrolled in the Optic Neuritis Treatment Trial to determine (1) whether loss and recovery of visual field sensitivity in …
PURPOSE: To compare the results of peripheral kinetic visual field testing and central static perimetry for pati …
A hand-held OKP chart for the screening of glaucoma: preliminary evaluation.
Damato BE, Chyla J, McClure E, Jay JL, Allan D. Damato BE, et al. Eye (Lond). 1990;4 ( Pt 4):632-7. doi: 10.1038/eye.1990.88. Eye (Lond). 1990. PMID: 2226995
Oculo-kinetic perimetry (OKP) uses controlled movements of the patient's eye to position a static test stimulus in the visual field. ...Ninety-eight eyes of 54 patients attending a hospital glaucoma clinic were tested with a prototype OKP glauco …
Oculo-kinetic perimetry (OKP) uses controlled movements of the patient's eye to position a static test stimulus in the …
Patterns of peripapillary retinal nerve fiber layer thinning in vigabatrin-exposed individuals.
Clayton LM, Devile M, Punte T, de Haan GJ, Sander JW, Acheson JF, Sisodiya SM. Clayton LM, et al. Ophthalmology. 2012 Oct;119(10):2152-60. doi: 10.1016/j.ophtha.2012.05.009. Epub 2012 Jul 30. Ophthalmology. 2012. PMID: 22853973
PURPOSE: To explore the relationship of peripapillary retinal nerve fiber layer (ppRNFL) thinning in individuals exposed to the antiepileptic drug vigabatrin with respect to 2 separate variables: cumulative vigabatrin exposure and severity of vigabatrin-associated visual …
PURPOSE: To explore the relationship of peripapillary retinal nerve fiber layer (ppRNFL) thinning in individuals exposed to the antiepilepti …
13 results