Mir TS - Search Results

1

The transition of pediatric Marfan patients to adult care: a challenge and its risks.

Stark VC, Doering K, von Kodolitsch Y, Kozlik-Feldmann R, Mueller GC, Olfe J, Rybczynski M, Schueler H, Mir TS. Stark VC, et al. Among authors: mir ts. Cardiovasc Diagn Ther. 2018 Dec;8(6):698-704. doi: 10.21037/cdt.2018.09.13. Cardiovasc Diagn Ther. 2018. PMID: 30740317 Free PMC article.

2

The spectrum of syndromes and manifestations in individuals screened for suspected Marfan syndrome.

Rybczynski M, Bernhardt AM, Rehder U, Fuisting B, Meiss L, Voss U, Habermann C, Detter C, Robinson PN, Arslan-Kirchner M, Schmidtke J, Mir TS, Berger J, Meinertz T, von Kodolitsch Y. Rybczynski M, et al. Among authors: mir ts. Am J Med Genet A. 2008 Dec 15;146A(24):3157-66. doi: 10.1002/ajmg.a.32595. Am J Med Genet A. 2008. PMID: 19012347

3

Augmentation index relates to progression of aortic disease in adults with Marfan syndrome.

Mortensen K, Aydin MA, Rybczynski M, Baulmann J, Schahidi NA, Kean G, Kühne K, Bernhardt AM, Franzen O, Mir T, Habermann C, Koschyk D, Ventura R, Willems S, Robinson PN, Berger J, Reichenspurner H, Meinertz T, von Kodolitsch Y. Mortensen K, et al. Am J Hypertens. 2009 Sep;22(9):971-9. doi: 10.1038/ajh.2009.115. Epub 2009 Jul 2. Am J Hypertens. 2009. PMID: 19574960

4

Marfan syndrome and the evolving spectrum of heritable thoracic aortic disease: do we need genetics for clinical decisions?

von Kodolitsch Y, Rybczynski M, Bernhardt A, Mir TS, Treede H, Dodge-Khatami A, Robinson PN, Sheikhzadeh S, Reichenspurner H, Meinertz T. von Kodolitsch Y, et al. Among authors: mir ts. Vasa. 2010 Feb;39(1):17-32. doi: 10.1024/0301-1526/a000002. Vasa. 2010. PMID: 20186673 Review.

5

A novel innominate vein-to-common atrium fenestration at Fontan completion.

Mir TS, Arndt F, von Samson P, Philipp L, Schnegg C, Mueller G, Dodge-Khatami A. Mir TS, et al. Ann Thorac Surg. 2010 May;89(5):e38-40. doi: 10.1016/j.athoracsur.2010.02.105. Ann Thorac Surg. 2010. PMID: 20417742

6

Dural ectasia in individuals with Marfan-like features but exclusion of mutations in the genes FBN1, TGFBR1 and TGFBR2.

Sheikhzadeh S, Rybczynski M, Habermann CR, Bernhardt AM, Arslan-Kirchner M, Keyser B, Kaemmerer H, Mir TS, Staebler A, Oezdal N, Robinson PN, Berger J, Meinertz T, von Kodolitsch Y. Sheikhzadeh S, et al. Among authors: mir ts. Clin Genet. 2011 Jun;79(6):568-74. doi: 10.1111/j.1399-0004.2010.01494.x. Clin Genet. 2011. PMID: 20662850

7

[Analysis of costs and profits of ambulatory care of Marfan patients after initiation of a novel German legal directive (116 b SGB V)].

Manow ML, Paulsen N, Rybczynski M, Mir T, Bernhardt AM, Treede H, Ohm G, Fuisting B, Rehder U, Meier F, Vogler M, Meinertz T, Overlack K, von Kodolitsch Y. Manow ML, et al. Med Klin (Munich). 2010 Aug;105(8):529-37. doi: 10.1007/s00063-010-1090-y. Epub 2010 Sep 8. Med Klin (Munich). 2010. PMID: 20824410 German.

8

Frequency and age-related course of mitral valve dysfunction in the Marfan syndrome.

Rybczynski M, Mir TS, Sheikhzadeh S, Bernhardt AM, Schad C, Treede H, Veldhoen S, Groene EF, Kühne K, Koschyk D, Robinson PN, Berger J, Reichenspurner H, Meinertz T, von Kodolitsch Y. Rybczynski M, et al. Among authors: mir ts. Am J Cardiol. 2010 Oct 1;106(7):1048-53. doi: 10.1016/j.amjcard.2010.05.038. Am J Cardiol. 2010. PMID: 20854973

9

Predictors of outcome of mitral valve prolapse in patients with the Marfan syndrome.

Rybczynski M, Treede H, Sheikhzadeh S, Groene EF, Bernhardt AM, Hillebrand M, Mir TS, Kühne K, Koschyk D, Robinson PN, Berger J, Reichenspurner H, Meinertz T, von Kodolitsch Y. Rybczynski M, et al. Among authors: mir ts. Am J Cardiol. 2011 Jan 15;107(2):268-74. doi: 10.1016/j.amjcard.2010.08.070. Am J Cardiol. 2011. PMID: 21211604

10

Analysis of phenotype and genotype information for the diagnosis of Marfan syndrome.

Sheikhzadeh S, Kade C, Keyser B, Stuhrmann M, Arslan-Kirchner M, Rybczynski M, Bernhardt AM, Habermann CR, Hillebrand M, Mir T, Robinson PN, Berger J, Detter C, Blankenberg S, Schmidtke J, von Kodolitsch Y. Sheikhzadeh S, et al. Clin Genet. 2012 Sep;82(3):240-7. doi: 10.1111/j.1399-0004.2011.01771.x. Epub 2011 Oct 5. Clin Genet. 2012. PMID: 21883168

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