Ozcelik C - Search Results

1

Recurrent in-stent restenosis is not associated with the angiotensin-converting enzyme D/I, angiotensinogen Thr174Met and Met235Thr, and the angiotensin-II receptor 1 A1166C polymorphism.

Gross CM, Perrot A, Geier C, Posch MG, Hassfeld S, Kramer J, Schmidt S, Derer W, Dietz R, Ozcelik C. Gross CM, et al. Among authors: ozcelik c. J Invasive Cardiol. 2007 Jun;19(6):261-4. J Invasive Cardiol. 2007. PMID: 17541127

2

Subacute coronary stent thrombosis in cancer patients.

Gross CM, Posch MG, Geier C, Olthoff H, Krämer J, Dechend R, Dietz R, Ozcelik C. Gross CM, et al. Among authors: ozcelik c. J Am Coll Cardiol. 2008 Mar 25;51(12):1232-3. doi: 10.1016/j.jacc.2007.11.061. J Am Coll Cardiol. 2008. PMID: 18355663 Free article. No abstract available.

3

Angiotensin-converting enzyme inhibition, autonomic activity, and hemodynamics in patients with heart failure who perform isometric exercise.

Willenbrock R, Ozcelik C, Osterziel KJ, Dietz R. Willenbrock R, et al. Among authors: ozcelik c. Am Heart J. 1996 May;131(5):999-1006. doi: 10.1016/s0002-8703(96)90186-6. Am Heart J. 1996. PMID: 8615323 Clinical Trial.

4

Mutations in the EGF-CFC gene cryptic are an infrequent cause of congenital heart disease.

Ozcelik C, Bit-Avragim N, Panek A, Gaio U, Geier C, Lange PE, Dietz R, Posch MG, Perrot A, Stiller B. Ozcelik C, et al. Pediatr Cardiol. 2006 Nov-Dec;27(6):695-8. doi: 10.1007/s00246-006-1082-0. Epub 2006 Oct 27. Pediatr Cardiol. 2006. PMID: 17072672

5

Mutations in GATA4, NKX2.5, CRELD1, and BMP4 are infrequently found in patients with congenital cardiac septal defects.

Posch MG, Perrot A, Schmitt K, Mittelhaus S, Esenwein EM, Stiller B, Geier C, Dietz R, Gessner R, Ozcelik C, Berger F. Posch MG, et al. Among authors: ozcelik c. Am J Med Genet A. 2008 Jan 15;146A(2):251-3. doi: 10.1002/ajmg.a.32042. Am J Med Genet A. 2008. PMID: 18076106 No abstract available.

6

Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy.

Geier C, Gehmlich K, Ehler E, Hassfeld S, Perrot A, Hayess K, Cardim N, Wenzel K, Erdmann B, Krackhardt F, Posch MG, Osterziel KJ, Bublak A, Nägele H, Scheffold T, Dietz R, Chien KR, Spuler S, Fürst DO, Nürnberg P, Ozcelik C. Geier C, et al. Among authors: ozcelik c. Hum Mol Genet. 2008 Sep 15;17(18):2753-65. doi: 10.1093/hmg/ddn160. Epub 2008 May 27. Hum Mol Genet. 2008. PMID: 18505755

7

Connective tissue growth factor overexpression in cardiomyocytes promotes cardiac hypertrophy and protection against pressure overload.

Panek AN, Posch MG, Alenina N, Ghadge SK, Erdmann B, Popova E, Perrot A, Geier C, Dietz R, Morano I, Bader M, Ozcelik C. Panek AN, et al. Among authors: ozcelik c. PLoS One. 2009 Aug 25;4(8):e6743. doi: 10.1371/journal.pone.0006743. PLoS One. 2009. PMID: 19707545 Free PMC article.

8

Molecular genetics of congenital atrial septal defects.

Posch MG, Perrot A, Berger F, Ozcelik C. Posch MG, et al. Among authors: ozcelik c. Clin Res Cardiol. 2010 Mar;99(3):137-47. doi: 10.1007/s00392-009-0095-0. Epub 2009 Dec 11. Clin Res Cardiol. 2010. PMID: 20012542 Free PMC article. Review.

9

The G-231A polymorphism in the endothelin-A receptor gene is associated with lower aortic pressure in patients with dilated cardiomyopathy.

Telgmann R, Harb BA, Ozcelik C, Perrot A, Schönfelder J, Nonnenmacher A, Brand M, Schmidt-Petersen K, Dietz R, Kreutz R, Osterziel KJ, Paul M, Brand-Herrmann SM. Telgmann R, et al. Among authors: ozcelik c. Am J Hypertens. 2007 Jan;20(1):32-7. doi: 10.1016/j.amjhyper.2006.06.016. Am J Hypertens. 2007. PMID: 17198909

10

Sequence analysis of myozenin 2 in 438 European patients with familial hypertrophic cardiomyopathy.

Posch MG, Thiemann L, Tomasov P, Veselka J, Cardim N, Garcia-Castro M, Coto E, Perrot A, Geier C, Dietz R, Haverkamp W, Ozcelik C. Posch MG, et al. Among authors: ozcelik c. Med Sci Monit. 2008 Jul;14(7):CR372-4. Med Sci Monit. 2008. PMID: 18591919

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