Banin E - Search Results

1

Nonsyndromic Early-Onset Cone-Rod Dystrophy and Limb-Girdle Muscular Dystrophy in a Consanguineous Israeli Family are Caused by Two Independent yet Linked Mutations in ALMS1 and DYSF.

Lazar CH, Kimchi A, Namburi P, Mutsuddi M, Zelinger L, Beryozkin A, Ben-Simhon S, Obolensky A, Ben-Neriah Z, Argov Z, Pikarsky E, Fellig Y, Marks-Ohana D, Ratnapriya R, Banin E, Sharon D, Swaroop A. Lazar CH, et al. Among authors: banin e. Hum Mutat. 2015 Sep;36(9):836-41. doi: 10.1002/humu.22822. Epub 2015 Jul 14. Hum Mutat. 2015. PMID: 26077327 Free PMC article.

2

Gene delivery by viral vectors in primary cultures of lacrimal gland tissue.

Banin E, Obolensky A, Piontek E, Falk H, Pikarsky E, Pe'er J, Panet A, Chowers I. Banin E, et al. Invest Ophthalmol Vis Sci. 2003 Apr;44(4):1529-33. doi: 10.1167/iovs.02-0529. Invest Ophthalmol Vis Sci. 2003. PMID: 12657589

3

Retinal function abnormalities in patients treated with vigabatrin.

Banin E, Shalev RS, Obolensky A, Neis R, Chowers I, Gross-Tsur V. Banin E, et al. Arch Ophthalmol. 2003 Jun;121(6):811-6. doi: 10.1001/archopht.121.6.811. Arch Ophthalmol. 2003. PMID: 12796251

4

Injury induced by chemical warfare agents: characterization and treatment of ocular tissues exposed to nitrogen mustard.

Banin E, Morad Y, Berenshtein E, Obolensky A, Yahalom C, Goldich J, Adibelli FM, Zuniga G, DeAnda M, Pe'er J, Chevion M. Banin E, et al. Invest Ophthalmol Vis Sci. 2003 Jul;44(7):2966-72. doi: 10.1167/iovs.02-1164. Invest Ophthalmol Vis Sci. 2003. PMID: 12824239

5

Retinal incorporation and differentiation of neural precursors derived from human embryonic stem cells.

Banin E, Obolensky A, Idelson M, Hemo I, Reinhardtz E, Pikarsky E, Ben-Hur T, Reubinoff B. Banin E, et al. Stem Cells. 2006 Feb;24(2):246-57. doi: 10.1634/stemcells.2005-0009. Epub 2005 Aug 25. Stem Cells. 2006. PMID: 16123388

6

Phenotypic variability among adult siblings with Sjögren-Larsson syndrome.

Lossos A, Khoury M, Rizzo WB, Gomori JM, Banin E, Zlotogorski A, Jaber S, Abramsky O, Argov Z, Rosenmann H. Lossos A, et al. Among authors: banin e. Arch Neurol. 2006 Feb;63(2):278-80. doi: 10.1001/archneur.63.2.278. Arch Neurol. 2006. PMID: 16476818 Free PMC article.

7

Novel USH2A mutations in Israeli patients with retinitis pigmentosa and Usher syndrome type 2.

Kaiserman N, Obolensky A, Banin E, Sharon D. Kaiserman N, et al. Among authors: banin e. Arch Ophthalmol. 2007 Feb;125(2):219-24. doi: 10.1001/archopht.125.2.219. Arch Ophthalmol. 2007. PMID: 17296898

8

A non-ancestral RPGR missense mutation in families with either recessive or semi-dominant X-linked retinitis pigmentosa.

Banin E, Mizrahi-Meissonnier L, Neis R, Silverstein S, Magyar I, Abeliovich D, Roepman R, Berger W, Rosenberg T, Sharon D. Banin E, et al. Am J Med Genet A. 2007 Jun 1;143A(11):1150-8. doi: 10.1002/ajmg.a.31642. Am J Med Genet A. 2007. PMID: 17480003

9

A complex expression pattern of Pax6 in the pigeon retina.

Bandah D, Swissa T, Ben-Shlomo G, Banin E, Ofri R, Sharon D. Bandah D, et al. Among authors: banin e. Invest Ophthalmol Vis Sci. 2007 Jun;48(6):2503-9. doi: 10.1167/iovs.06-1014. Invest Ophthalmol Vis Sci. 2007. PMID: 17525177

10

Homozygosity for a novel ABCA4 founder splicing mutation is associated with progressive and severe Stargardt-like disease.

Beit-Ya'acov A, Mizrahi-Meissonnier L, Obolensky A, Landau C, Blumenfeld A, Rosenmann A, Banin E, Sharon D. Beit-Ya'acov A, et al. Among authors: banin e. Invest Ophthalmol Vis Sci. 2007 Sep;48(9):4308-14. doi: 10.1167/iovs.07-0244. Invest Ophthalmol Vis Sci. 2007. PMID: 17724221

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