Mardin CY - Search Results

1

Exploring functional candidate genes for genetic association in german patients with pseudoexfoliation syndrome and pseudoexfoliation glaucoma.

Krumbiegel M, Pasutto F, Mardin CY, Weisschuh N, Paoli D, Gramer E, Zenkel M, Weber BH, Kruse FE, Schlötzer-Schrehardt U, Reis A. Krumbiegel M, et al. Among authors: mardin cy. Invest Ophthalmol Vis Sci. 2009 Jun;50(6):2796-801. doi: 10.1167/iovs.08-2339. Epub 2009 Jan 31. Invest Ophthalmol Vis Sci. 2009. PMID: 19182256 Free article.

2

Morphometry of the human lamina cribrosa surface.

Jonas JB, Mardin CY, Schlötzer-Schrehardt U, Naumann GO. Jonas JB, et al. Among authors: mardin cy. Invest Ophthalmol Vis Sci. 1991 Feb;32(2):401-5. Invest Ophthalmol Vis Sci. 1991. PMID: 1993592

3

[Early diagnosis of pseudoexfoliation syndrome. A clinical electron microscopy correlation of the central, anterior lens capsule].

Mardin CY, Schlötzer-Schrehardt U, Naumann GO. Mardin CY, et al. Klin Monbl Augenheilkd. 1997 Nov;211(5):296-300. doi: 10.1055/s-2008-1035138. Klin Monbl Augenheilkd. 1997. PMID: 9527586 German.

4

Expression of cyclooxygenase-1 and -2 in normal and glaucomatous human eyes.

Maihöfner C, Schlötzer-Schrehardt U, Gühring H, Zeilhofer HU, Naumann GO, Pahl A, Mardin C, Tamm ER, Brune K. Maihöfner C, et al. Invest Ophthalmol Vis Sci. 2001 Oct;42(11):2616-24. Invest Ophthalmol Vis Sci. 2001. PMID: 11581208 Free article.

5

"Masked" pseudoexfoliation syndrome in unoperated eyes with circular posterior synechiae: clinical-electron microscopic correlation.

Mardin CY, Schlötzer-Schrehardt U, Naumann GO. Mardin CY, et al. Arch Ophthalmol. 2001 Oct;119(10):1500-3. doi: 10.1001/archopht.119.10.1500. Arch Ophthalmol. 2001. PMID: 11594951

6

Monitoring glaucoma progression with visual evoked potentials of the blue-sensitive pathway.

Horn FK, Jonas JB, Budde WM, Jünemann AM, Mardin CY, Korth M. Horn FK, et al. Among authors: mardin cy. Invest Ophthalmol Vis Sci. 2002 Jun;43(6):1828-34. Invest Ophthalmol Vis Sci. 2002. PMID: 12036986

7

Novel mutations in the MYOC/GLC1A gene in a large group of glaucoma patients.

Michels-Rautenstrauss K, Mardin C, Wakili N, Jünemann AM, Villalobos L, Mejia C, Soley GC, Azofeifa J, Ozbey S, Naumann GO, Reis A, Rautenstrauss B. Michels-Rautenstrauss K, et al. Hum Mutat. 2002 Dec;20(6):479-80. doi: 10.1002/humu.9092. Hum Mutat. 2002. PMID: 12442283

8

[Impact of prostaglandin-F(2alpha)-analogues and carbonic anhydrase inhibitors on central corneal thickness -- a cross-sectional study on 403 eyes].

Viestenz A, Martus P, Schlötzer-Schrehardt U, Langenbucher A, Mardin CY. Viestenz A, et al. Among authors: mardin cy. Klin Monbl Augenheilkd. 2004 Sep;221(9):753-6. doi: 10.1055/s-2004-81361. Klin Monbl Augenheilkd. 2004. PMID: 15459842 Clinical Trial. German.

9

Primary congenital glaucoma and Rieger's anomaly: extended haplotypes reveal founder effects for eight distinct CYP1B1 mutations.

Chavarria-Soley G, Michels-Rautenstrauss K, Pasutto F, Flikier D, Flikier P, Cirak S, Bejjani B, Winters DL, Lewis RA, Mardin C, Reis A, Rautenstrauss B. Chavarria-Soley G, et al. Mol Vis. 2006 May 22;12:523-31. Mol Vis. 2006. PMID: 16735994 Free article.

10

Profiling of WDR36 missense variants in German patients with glaucoma.

Pasutto F, Mardin CY, Michels-Rautenstrauss K, Weber BH, Sticht H, Chavarria-Soley G, Rautenstrauss B, Kruse F, Reis A. Pasutto F, et al. Among authors: mardin cy. Invest Ophthalmol Vis Sci. 2008 Jan;49(1):270-4. doi: 10.1167/iovs.07-0500. Invest Ophthalmol Vis Sci. 2008. PMID: 18172102 Free article.

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