Chowers I - Search Results

1

Novel null mutations in the EYS gene are a frequent cause of autosomal recessive retinitis pigmentosa in the Israeli population.

Bandah-Rozenfeld D, Littink KW, Ben-Yosef T, Strom TM, Chowers I, Collin RW, den Hollander AI, van den Born LI, Zonneveld MN, Merin S, Banin E, Cremers FP, Sharon D. Bandah-Rozenfeld D, et al. Among authors: chowers i. Invest Ophthalmol Vis Sci. 2010 Sep;51(9):4387-94. doi: 10.1167/iovs.09-4732. Epub 2010 Apr 7. Invest Ophthalmol Vis Sci. 2010. PMID: 20375346 Free article.

2

[Experimental therapeutic modalities for retinitis pigmentosa].

Chowers I, Banin E. Chowers I, et al. Harefuah. 2003 Apr;142(4):277-80, 317. Harefuah. 2003. PMID: 12754878 Review. Hebrew.

3

[Experimental therapeutic modalities for retinitis pigmentosa].

Banin E, Chowers I. Banin E, et al. Among authors: chowers i. Harefuah. 2004 May;143(5):368-71, 389. Harefuah. 2004. PMID: 15190851 Review. Hebrew.

4

Homozygosity mapping reveals null mutations in FAM161A as a cause of autosomal-recessive retinitis pigmentosa.

Bandah-Rozenfeld D, Mizrahi-Meissonnier L, Farhy C, Obolensky A, Chowers I, Pe'er J, Merin S, Ben-Yosef T, Ashery-Padan R, Banin E, Sharon D. Bandah-Rozenfeld D, et al. Among authors: chowers i. Am J Hum Genet. 2010 Sep 10;87(3):382-91. doi: 10.1016/j.ajhg.2010.07.022. Epub 2010 Aug 12. Am J Hum Genet. 2010. PMID: 20705279 Free PMC article.

5

Mutations in CRB1 are a relatively common cause of autosomal recessive early-onset retinal degeneration in the Israeli and Palestinian populations.

Beryozkin A, Zelinger L, Bandah-Rozenfeld D, Harel A, Strom TA, Merin S, Chowers I, Banin E, Sharon D. Beryozkin A, et al. Among authors: chowers i. Invest Ophthalmol Vis Sci. 2013 Mar 1;54(3):2068-75. doi: 10.1167/iovs.12-11419. Invest Ophthalmol Vis Sci. 2013. PMID: 23449718

6

The Genetics of Usher Syndrome in the Israeli and Palestinian Populations.

Khalaileh A, Abu-Diab A, Ben-Yosef T, Raas-Rothschild A, Lerer I, Alswaiti Y, Chowers I, Banin E, Sharon D, Khateb S. Khalaileh A, et al. Among authors: chowers i. Invest Ophthalmol Vis Sci. 2018 Feb 1;59(2):1095-1104. doi: 10.1167/iovs.17-22817. Invest Ophthalmol Vis Sci. 2018. PMID: 29490346

7

A novel intronic mutation of PDE6B is a major cause of autosomal recessive retinitis pigmentosa among Caucasus Jews.

Tatour Y, Tamaiev J, Shamaly S, Colombo R, Bril E, Rabinowitz T, Yaakobi A, Mezer E, Leibu R, Tiosano B, Shomron N, Chowers I, Banin E, Sharon D, Ben-Yosef T. Tatour Y, et al. Among authors: chowers i. Mol Vis. 2019 Feb 22;25:155-164. eCollection 2019. Mol Vis. 2019. PMID: 30820151 Free PMC article.

8

Unique combination of clinical features in a large cohort of 100 patients with retinitis pigmentosa caused by FAM161A mutations.

Beryozkin A, Khateb S, Idrobo-Robalino CA, Khan MI, Cremers FPM, Obolensky A, Hanany M, Mezer E, Chowers I, Newman H, Ben-Yosef T, Sharon D, Banin E. Beryozkin A, et al. Among authors: chowers i. Sci Rep. 2020 Sep 16;10(1):15156. doi: 10.1038/s41598-020-72028-0. Sci Rep. 2020. PMID: 32938956 Free PMC article.

9

A pilot study of topical treatment with an alpha2-agonist in patients with retinal dystrophies.

Merin S, Obolensky A, Farber MD, Chowers I. Merin S, et al. Among authors: chowers i. J Ocul Pharmacol Ther. 2008 Feb;24(1):80-6. doi: 10.1089/jop.2007.0022. J Ocul Pharmacol Ther. 2008. PMID: 18201138 Clinical Trial.

10

Retinal function and structure in the hypotransferrinemic mouse.

Lederman M, Obolensky A, Grunin M, Banin E, Chowers I. Lederman M, et al. Among authors: chowers i. Invest Ophthalmol Vis Sci. 2012 Feb 2;53(2):605-12. doi: 10.1167/iovs.11-7436. Invest Ophthalmol Vis Sci. 2012. PMID: 22159020

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