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Michael P Clarke

Showing results (31-40 of 40) with videos related to

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Trials|October 18, 2012
Surgery versus Active Monitoring in Intermittent Exotropia (SamExo): study protocol for a pilot randomised controlled trialDeborah Buck, Elaine McColl, Christine J Powell, et al.
BMC Ophthalmology|January 20, 2012
The improving outcomes in intermittent exotropia study: outcomes at 2 years after diagnosis in an observational cohortDeborah Buck, Christine J Powell, Jugnoo Rahi, et al.
European Journal of Human Genetics : EJHG|April 5, 2007
Inherited PAX6, NF1 and OTX2 mutations in a child with microphthalmia and aniridiaR Alex Henderson, Kathy Williamson, Sally Cumming, et al.
Biochimica Et Biophysica Acta|April 17, 2003
Expression of ADAMTS metalloproteinases in the retinal pigment epithelium derived cell line ARPE-19: transcriptional regulation by TNFalphaDebra J Bevitt, Jeseem Mohamed, Jon B Catterall, et al.
Plos One|November 8, 2019
Characterizing the Randot Preschool stereotest: Testability, norms, reliability, specificity and sensitivity in children aged 2-11 yearsJenny C A Read, Sheima Rafiq, Jess Hugill, et al.
Ophthalmology|April 27, 2010
The prevalence and natural history of dominant optic atrophy due to OPA1 mutationsPatrick Yu-Wai-Man, Philip G Griffiths, Ailbhe Burke, et al.
Ophthalmology|June 13, 2013
A randomized trial of increasing patching for amblyopia, David K Wallace, Elizabeth L Lazar, et al.
Translational Vision Science & Technology|March 6, 2019
ASTEROID: A New Clinical Stereotest on an Autostereo 3D TabletKathleen Vancleef, Ignacio Serrano-Pedraza, Craig Sharp, et al.
American Journal of Human Genetics|October 18, 2003
Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardationKathryn P Burdon, James D McKay, Michèle M Sale, et al.
American Journal of Human Genetics|April 23, 2005
Heterozygous mutations of OTX2 cause severe ocular malformationsNicola K Ragge, Alison G Brown, Charlotte M Poloschek, et al.
Pageof 4

Showing results (31-40 of 40) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 40 results.
Trials|October 18, 2012
Surgery versus Active Monitoring in Intermittent Exotropia (SamExo): study protocol for a pilot randomised controlled trialDeborah Buck, Elaine McColl, Christine J Powell, et al.
BMC Ophthalmology|January 20, 2012
The improving outcomes in intermittent exotropia study: outcomes at 2 years after diagnosis in an observational cohortDeborah Buck, Christine J Powell, Jugnoo Rahi, et al.
European Journal of Human Genetics : EJHG|April 5, 2007
Inherited PAX6, NF1 and OTX2 mutations in a child with microphthalmia and aniridiaR Alex Henderson, Kathy Williamson, Sally Cumming, et al.
Biochimica Et Biophysica Acta|April 17, 2003
Expression of ADAMTS metalloproteinases in the retinal pigment epithelium derived cell line ARPE-19: transcriptional regulation by TNFalphaDebra J Bevitt, Jeseem Mohamed, Jon B Catterall, et al.
Plos One|November 8, 2019
Characterizing the Randot Preschool stereotest: Testability, norms, reliability, specificity and sensitivity in children aged 2-11 yearsJenny C A Read, Sheima Rafiq, Jess Hugill, et al.
Ophthalmology|April 27, 2010
The prevalence and natural history of dominant optic atrophy due to OPA1 mutationsPatrick Yu-Wai-Man, Philip G Griffiths, Ailbhe Burke, et al.
Ophthalmology|June 13, 2013
A randomized trial of increasing patching for amblyopia, David K Wallace, Elizabeth L Lazar, et al.
Translational Vision Science & Technology|March 6, 2019
ASTEROID: A New Clinical Stereotest on an Autostereo 3D TabletKathleen Vancleef, Ignacio Serrano-Pedraza, Craig Sharp, et al.
American Journal of Human Genetics|October 18, 2003
Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardationKathryn P Burdon, James D McKay, Michèle M Sale, et al.
American Journal of Human Genetics|April 23, 2005
Heterozygous mutations of OTX2 cause severe ocular malformationsNicola K Ragge, Alison G Brown, Charlotte M Poloschek, et al.
Pageof 4