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Results: 1 to 20 of 161

Related Citations for PubMed (Select 18254956)

1.

DNA sequence variants in the LOXL1 gene are associated with pseudoexfoliation glaucoma in a U.S. clinic-based population with broad ethnic diversity.

Fan BJ, Pasquale L, Grosskreutz CL, Rhee D, Chen T, DeAngelis MM, Kim I, del Bono E, Miller JW, Li T, Haines JL, Wiggs JL.

BMC Med Genet. 2008 Feb 6;9:5. doi: 10.1186/1471-2350-9-5.

2.
3.

Exfoliation syndrome and exfoliation glaucoma-associated LOXL1 variations are not involved in pigment dispersion syndrome and pigmentary glaucoma.

Rao KN, Ritch R, Dorairaj SK, Kaur I, Liebmann JM, Thomas R, Chakrabarti S.

Mol Vis. 2008 Jul 9;14:1254-62.

4.

Association of LOXL1 polymorphisms with pseudoexfoliation in the Chinese.

Lee KY, Ho SL, Thalamuthu A, Venkatraman A, Venkataraman D, Pek DC, Aung T, Vithana EN.

Mol Vis. 2009 Jun 4;15:1120-6.

5.

Association of LOXL1 polymorphisms with pseudoexfoliation, glaucoma, intraocular pressure, and systemic diseases in a Greek population. The Thessaloniki eye study.

Anastasopoulos E, Coleman AL, Wilson MR, Sinsheimer JS, Yu F, Katafigiotis S, Founti P, Salonikiou A, Pappas T, Koskosas A, Katopodi T, Lambropoulos A, Topouzis F.

Invest Ophthalmol Vis Sci. 2014 Jun 10;55(7):4238-43. doi: 10.1167/iovs.14-13991.

6.

Association of LOXL1 common sequence variants in German and Italian patients with pseudoexfoliation syndrome and pseudoexfoliation glaucoma.

Pasutto F, Krumbiegel M, Mardin CY, Paoli D, Lämmer R, Weber BH, Kruse FE, Schlötzer-Schrehardt U, Reis A.

Invest Ophthalmol Vis Sci. 2008 Apr;49(4):1459-63. doi: 10.1167/iovs.07-1449.

7.

LOXL1 variants in elderly Japanese patients with exfoliation syndrome/glaucoma, primary open-angle glaucoma, normal tension glaucoma, and cataract.

Tanito M, Minami M, Akahori M, Kaidzu S, Takai Y, Ohira A, Iwata T.

Mol Vis. 2008;14:1898-905. Epub 2008 Oct 27.

8.

Evaluation of LOXL1 gene polymorphisms in exfoliation syndrome and exfoliation glaucoma.

Aragon-Martin JA, Ritch R, Liebmann J, O'Brien C, Blaaow K, Mercieca F, Spiteri A, Cobb CJ, Damji KF, Tarkkanen A, Rezaie T, Child AH, Sarfarazi M.

Mol Vis. 2008 Mar 17;14:533-41.

9.

Association of lysyl oxidase-like 1 gene common sequence variants in Greek patients with pseudoexfoliation syndrome and pseudoexfoliation glaucoma.

Metaxaki I, Constantoulakis P, Papadimitropoulos M, Filiou E, Georgopoulos G, Chamchougia A, Papakonstantinou D, Markomichelakis N, Koutsandrea C, Halkiadakis I.

Mol Vis. 2013 Jul 12;19:1446-52. Print 2013.

10.

LOXL1 promoter haplotypes are associated with exfoliation syndrome in a U.S. Caucasian population.

Fan BJ, Pasquale LR, Rhee D, Li T, Haines JL, Wiggs JL.

Invest Ophthalmol Vis Sci. 2011 Apr 12;52(5):2372-8. doi: 10.1167/iovs.10-6268. Print 2011 Apr.

11.

Prevalence of high-risk alleles in the LOXL1 gene and its association with pseudoexfoliation syndrome and exfoliation glaucoma in a Latin American population.

Jaimes M, Rivera-Parra D, Miranda-Duarte A, Valdés G, Zenteno JC.

Ophthalmic Genet. 2012 Mar;33(1):12-7. doi: 10.3109/13816810.2011.615078. Epub 2011 Oct 4.

PMID:
21970694
12.

Association of LOXL1 gene polymorphisms with exfoliation syndrome/glaucoma and primary open angle glaucoma in a Turkish population.

Kasım B, İrkeç M, Alikaşifoğlu M, Orhan M, Mocan MC, Aktaş D.

Mol Vis. 2013;19:114-20. Epub 2013 Jan 28.

13.

Lysyl oxidase-like 1 polymorphisms and exfoliation syndrome in the Japanese population.

Hayashi H, Gotoh N, Ueda Y, Nakanishi H, Yoshimura N.

Am J Ophthalmol. 2008 Mar;145(3):582-585. doi: 10.1016/j.ajo.2007.10.023. Epub 2008 Jan 16.

PMID:
18201684
14.

Lack of association between LOXL1 variants and primary open-angle glaucoma in three different populations.

Liu Y, Schmidt S, Qin X, Gibson J, Hutchins K, Santiago-Turla C, Wiggs JL, Budenz DL, Akafo S, Challa P, Herndon LW, Hauser MA, Allingham RR.

Invest Ophthalmol Vis Sci. 2008 Aug;49(8):3465-8. doi: 10.1167/iovs.08-1850. Epub 2008 Apr 17.

16.

Role of Lysyl oxidase-like 1 gene polymorphisms in Pakistani patients with pseudoexfoliative glaucoma.

Micheal S, Khan MI, Akhtar F, Ali M, Ahmed A, den Hollander AI, Qamar R.

Mol Vis. 2012;18:1040-4. Epub 2012 Apr 25.

17.

Association of LOXL1 gene polymorphisms with pseudoexfoliation in the Japanese.

Ozaki M, Lee KY, Vithana EN, Yong VH, Thalamuthu A, Mizoguchi T, Venkatraman A, Aung T.

Invest Ophthalmol Vis Sci. 2008 Sep;49(9):3976-80. doi: 10.1167/iovs.08-1805. Epub 2008 Apr 30.

18.

Evaluation of LOXL1 polymorphisms in eyes with exfoliation glaucoma in Japanese.

Fuse N, Miyazawa A, Nakazawa T, Mengkegale M, Otomo T, Nishida K.

Mol Vis. 2008 Jul 21;14:1338-43.

19.

Association of LOXL1 gene with Finnish exfoliation syndrome patients.

Lemmelä S, Forsman E, Onkamo P, Nurmi H, Laivuori H, Kivelä T, Puska P, Heger M, Eriksson A, Forsius H, Järvelä I.

J Hum Genet. 2009 May;54(5):289-97. doi: 10.1038/jhg.2009.28. Epub 2009 Apr 3.

PMID:
19343041
20.

Evaluation of LOXL1 polymorphisms in primary open-angle glaucoma in southern and northern Chinese.

Gong WF, Chiang SW, Chen LJ, Tam PO, Jia LY, Leung DY, Geng YQ, Tham CC, Lam DS, Ritch R, Wang N, Pang CP.

Mol Vis. 2008;14:2381-9. Epub 2008 Dec 19.

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