Lifshitz T - Search Results

1

COL11A2 mutation associated with autosomal recessive Weissenbacher-Zweymuller syndrome: molecular and clinical overlap with otospondylomegaepiphyseal dysplasia (OSMED).

Harel T, Rabinowitz R, Hendler N, Galil A, Flusser H, Chemke J, Gradstein L, Lifshitz T, Ofir R, Elbedour K, Birk OS. Harel T, et al. Among authors: lifshitz t. Am J Med Genet A. 2005 Jan 1;132A(1):33-5. doi: 10.1002/ajmg.a.30371. Am J Med Genet A. 2005. PMID: 15558753

2

Homozygous CRYBB1 deletion mutation underlies autosomal recessive congenital cataract.

Cohen D, Bar-Yosef U, Levy J, Gradstein L, Belfair N, Ofir R, Joshua S, Lifshitz T, Carmi R, Birk OS. Cohen D, et al. Among authors: lifshitz t. Invest Ophthalmol Vis Sci. 2007 May;48(5):2208-13. doi: 10.1167/iovs.06-1019. Invest Ophthalmol Vis Sci. 2007. PMID: 17460281

3

High myopia caused by a mutation in LEPREL1, encoding prolyl 3-hydroxylase 2.

Mordechai S, Gradstein L, Pasanen A, Ofir R, El Amour K, Levy J, Belfair N, Lifshitz T, Joshua S, Narkis G, Elbedour K, Myllyharju J, Birk OS. Mordechai S, et al. Among authors: lifshitz t. Am J Hum Genet. 2011 Sep 9;89(3):438-45. doi: 10.1016/j.ajhg.2011.08.003. Epub 2011 Sep 1. Am J Hum Genet. 2011. PMID: 21885030 Free PMC article.

4

Combined CNV, haplotyping and whole exome sequencing enable identification of two distinct novel EYS mutations causing RP in a single inbred tribe.

Wormser O, Gradstein L, Kadar E, Yogev Y, Perez Y, Mashkit E, Elbedour K, Drabkin M, Markus B, Kadir R, Halperin D, Khalaila S, Levy J, Lifshitz T, Manor E, Birk OS. Wormser O, et al. Among authors: lifshitz t. Am J Med Genet A. 2018 Dec;176(12):2695-2703. doi: 10.1002/ajmg.a.40668. Epub 2018 Dec 4. Am J Med Genet A. 2018. PMID: 30513137

5

The ocular manifestations of Weissenbacher-Zweymuller syndrome.

Rabinowitz R, Gradstein L, Galil A, Levy J, Lifshitz T. Rabinowitz R, et al. Among authors: lifshitz t. Eye (Lond). 2004 Dec;18(12):1258-63. doi: 10.1038/sj.eye.6701386. Eye (Lond). 2004. PMID: 15044941

6

Isolated foveal hypoplasia with secondary nystagmus and low vision is associated with a homozygous SLC38A8 mutation.

Perez Y, Gradstein L, Flusser H, Markus B, Cohen I, Langer Y, Marcus M, Lifshitz T, Kadir R, Birk OS. Perez Y, et al. Among authors: lifshitz t. Eur J Hum Genet. 2014 May;22(5):703-6. doi: 10.1038/ejhg.2013.212. Epub 2013 Sep 18. Eur J Hum Genet. 2014. PMID: 24045842 Free PMC article.

7

Novel GUCY2D mutation causes phenotypic variability of Leber congenital amaurosis in a large kindred.

Gradstein L, Zolotushko J, Sergeev YV, Lavy I, Narkis G, Perez Y, Guigui S, Sharon D, Banin E, Walter E, Lifshitz T, Birk OS. Gradstein L, et al. Among authors: lifshitz t. BMC Med Genet. 2016 Jul 30;17(1):52. doi: 10.1186/s12881-016-0314-2. BMC Med Genet. 2016. PMID: 27475985 Free PMC article.

8

Functional visual loss in patients with bilateral ocular coloboma.

Gradstein L, Belfair N, Ronen E, Lifshitz T, Biedner B. Gradstein L, et al. Among authors: lifshitz t. J AAPOS. 2002 Jun;6(3):195-7. doi: 10.1067/mpa.2002.122679. J AAPOS. 2002. PMID: 12075298 No abstract available.

9

Consecutive central retinal artery and vein occlusions in primary antiphospholipid syndrome.

Levy J, Baumgarten A, Rosenthal G, Rabinowitz R, Lifshitz T. Levy J, et al. Among authors: lifshitz t. Retina. 2002 Dec;22(6):784-6. doi: 10.1097/00006982-200212000-00016. Retina. 2002. PMID: 12476107 No abstract available.

10

Acinetobacter corneal graft ulcer and endophthalmitis: report of two cases.

Levy J, Oshry T, Rabinowitz R, Lifshitz T. Levy J, et al. Among authors: lifshitz t. Can J Ophthalmol. 2005 Feb;40(1):79-82. doi: 10.1016/S0008-4182(05)80123-1. Can J Ophthalmol. 2005. PMID: 15825536 No abstract available.

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