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Saul Merin

Showing results (1-10 of 11) with videos related to

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Journal of Ocular Pharmacology and Therapeutics : the Official Journal of the Association for Ocular Pharmacology and Therapeutics|January 19, 2008
A pilot study of topical treatment with an alpha2-agonist in patients with retinal dystrophiesSaul Merin, Alexey Obolensky, Marilyn D Farber, et al.
Investigative Ophthalmology & Visual Science|March 12, 2010
Variable retinal phenotypes caused by mutations in the X-linked photopigment gene arrayLiliana Mizrahi-Meissonnier, Saul Merin, Eyal Banin, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 11, 2009
The spectrum of retinal diseases caused by NR2E3 mutations in Israeli and Palestinian patientsDikla Bandah, Saul Merin, Munther Ashhab, et al.
Journal of Cataract and Refractive Surgery|November 8, 2003
Wiping microkeratome blades with sterile 100% alcohol to prevent diffuse lamellar keratitis after laser in situ keratomileusisSamuel Levinger, David Landau, Israel Kremer, et al.
Plos One|December 20, 2012
Exome sequencing identifies a founder frameshift mutation in an alternative exon of USH1C as the cause of autosomal recessive retinitis pigmentosa with late-onset hearing lossSamer Khateb, Lina Zelinger, Tamar Ben-Yosef, et al.
Investigative Ophthalmology & Visual Science|March 2, 2013
Mutations in CRB1 are a relatively common cause of autosomal recessive early-onset retinal degeneration in the Israeli and Palestinian populationsAvigail Beryozkin, Lina Zelinger, Dikla Bandah-Rozenfeld, et al.
Investigative Ophthalmology & Visual Science|January 30, 2014
Identification of mutations causing inherited retinal degenerations in the israeli and palestinian populations using homozygosity mappingAvigail Beryozkin, Lina Zelinger, Dikla Bandah-Rozenfeld, et al.
American Journal of Human Genetics|August 14, 2010
Homozygosity mapping reveals null mutations in FAM161A as a cause of autosomal-recessive retinitis pigmentosaDikla Bandah-Rozenfeld, Liliana Mizrahi-Meissonnier, Chen Farhy, et al.
American Journal of Human Genetics|December 29, 2005
Comparative genomics and gene expression analysis identifies BBS9, a new Bardet-Biedl syndrome geneDarryl Y Nishimura, Ruth E Swiderski, Charles C Searby, et al.
American Journal of Human Genetics|February 8, 2011
A missense mutation in DHDDS, encoding dehydrodolichyl diphosphate synthase, is associated with autosomal-recessive retinitis pigmentosa in Ashkenazi JewsLina Zelinger, Eyal Banin, Alexey Obolensky, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Journal of Ocular Pharmacology and Therapeutics : the Official Journal of the Association for Ocular Pharmacology and Therapeutics|January 19, 2008
A pilot study of topical treatment with an alpha2-agonist in patients with retinal dystrophiesSaul Merin, Alexey Obolensky, Marilyn D Farber, et al.
Investigative Ophthalmology & Visual Science|March 12, 2010
Variable retinal phenotypes caused by mutations in the X-linked photopigment gene arrayLiliana Mizrahi-Meissonnier, Saul Merin, Eyal Banin, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 11, 2009
The spectrum of retinal diseases caused by NR2E3 mutations in Israeli and Palestinian patientsDikla Bandah, Saul Merin, Munther Ashhab, et al.
Journal of Cataract and Refractive Surgery|November 8, 2003
Wiping microkeratome blades with sterile 100% alcohol to prevent diffuse lamellar keratitis after laser in situ keratomileusisSamuel Levinger, David Landau, Israel Kremer, et al.
Plos One|December 20, 2012
Exome sequencing identifies a founder frameshift mutation in an alternative exon of USH1C as the cause of autosomal recessive retinitis pigmentosa with late-onset hearing lossSamer Khateb, Lina Zelinger, Tamar Ben-Yosef, et al.
Investigative Ophthalmology & Visual Science|March 2, 2013
Mutations in CRB1 are a relatively common cause of autosomal recessive early-onset retinal degeneration in the Israeli and Palestinian populationsAvigail Beryozkin, Lina Zelinger, Dikla Bandah-Rozenfeld, et al.
Investigative Ophthalmology & Visual Science|January 30, 2014
Identification of mutations causing inherited retinal degenerations in the israeli and palestinian populations using homozygosity mappingAvigail Beryozkin, Lina Zelinger, Dikla Bandah-Rozenfeld, et al.
American Journal of Human Genetics|August 14, 2010
Homozygosity mapping reveals null mutations in FAM161A as a cause of autosomal-recessive retinitis pigmentosaDikla Bandah-Rozenfeld, Liliana Mizrahi-Meissonnier, Chen Farhy, et al.
American Journal of Human Genetics|December 29, 2005
Comparative genomics and gene expression analysis identifies BBS9, a new Bardet-Biedl syndrome geneDarryl Y Nishimura, Ruth E Swiderski, Charles C Searby, et al.
American Journal of Human Genetics|February 8, 2011
A missense mutation in DHDDS, encoding dehydrodolichyl diphosphate synthase, is associated with autosomal-recessive retinitis pigmentosa in Ashkenazi JewsLina Zelinger, Eyal Banin, Alexey Obolensky, et al.
Pageof 2