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Page 1
Pregnancy in adults with congenital heart disease.
Zengin E, Mueller G, Blankenberg S, von Kodolitsch Y, Rickers C, Sinning C. Zengin E, et al. Among authors: von kodolitsch y. Cardiovasc Diagn Ther. 2019 Oct;9(Suppl 2):S416-S423. doi: 10.21037/cdt.2019.07.01. Cardiovasc Diagn Ther. 2019. PMID: 31737546 Free PMC article. Review.
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. Among authors: von kodolitsch y. 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
A simple clinical model to estimate the probability of Marfan syndrome.
Sheikhzadeh S, Kusch ML, Rybczynski M, Kade C, Keyser B, Bernhardt AM, Hillebrand M, Mir TS, Fuisting B, Robinson PN, Berger J, Lorenzen V, Schmidtke J, Blankenberg S, von Kodolitsch Y. Sheikhzadeh S, et al. Among authors: von kodolitsch y. QJM. 2012 Jun;105(6):527-35. doi: 10.1093/qjmed/hcs008. Epub 2012 Feb 1. QJM. 2012. PMID: 22301820 Clinical Trial.
Comprehensive analysis of dural ectasia in 150 patients with a causative FBN1 mutation.
Sheikhzadeh S, Sondermann C, Rybczynski M, Habermann CR, Brockstaedt L, Keyser B, Kaemmerer H, Mir T, Staebler A, Robinson PN, Kutsche K, Berger J, Blankenberg S, von Kodolitsch Y. Sheikhzadeh S, et al. Among authors: von kodolitsch y. Clin Genet. 2014 Sep;86(3):238-45. doi: 10.1111/cge.12264. Epub 2013 Sep 23. Clin Genet. 2014. PMID: 23991918
Observational cohort study of ventricular arrhythmia in adults with Marfan syndrome caused by FBN1 mutations.
Aydin A, Adsay BA, Sheikhzadeh S, Keyser B, Rybczynski M, Sondermann C, Detter C, Steven D, Robinson PN, Berger J, Schmidtke J, Blankenberg S, Willems S, von Kodolitsch Y, Hoffmann BA. Aydin A, et al. Among authors: von kodolitsch y. PLoS One. 2013 Dec 13;8(12):e81281. doi: 10.1371/journal.pone.0081281. eCollection 2013. PLoS One. 2013. PMID: 24349050 Free PMC article.
Total serum transforming growth factor-β1 is elevated in the entire spectrum of genetic aortic syndromes.
Hillebrand M, Millot N, Sheikhzadeh S, Rybczynski M, Gerth S, Kölbel T, Keyser B, Kutsche K, Robinson PN, Berger J, Mir TS, Zeller T, Blankenberg S, von Kodolitsch Y, Goldmann B. Hillebrand M, et al. Among authors: von kodolitsch y. Clin Cardiol. 2014 Nov;37(11):672-9. doi: 10.1002/clc.22320. Epub 2014 Aug 11. Clin Cardiol. 2014. PMID: 25113270 Free PMC article.
The main pulmonary artery in adults: a controlled multicenter study with assessment of echocardiographic reference values, and the frequency of dilatation and aneurysm in Marfan syndrome.
Sheikhzadeh S, De Backer J, Gorgan NR, Rybczynski M, Hillebrand M, Schüler H, Bernhardt AM, Koschyk D, Bannas P, Keyser B, Mortensen K, Radke RM, Mir TS, Kölbel T, Robinson PN, Schmidtke J, Berger J, Blankenberg S, von Kodolitsch Y. Sheikhzadeh S, et al. Among authors: von kodolitsch y. Orphanet J Rare Dis. 2014 Dec 10;9:203. doi: 10.1186/s13023-014-0203-8. Orphanet J Rare Dis. 2014. PMID: 25491897 Free PMC article.
Perspectives on the revised Ghent criteria for the diagnosis of Marfan syndrome.
von Kodolitsch Y, De Backer J, Schüler H, Bannas P, Behzadi C, Bernhardt AM, Hillebrand M, Fuisting B, Sheikhzadeh S, Rybczynski M, Kölbel T, Püschel K, Blankenberg S, Robinson PN. von Kodolitsch Y, et al. Appl Clin Genet. 2015 Jun 16;8:137-55. doi: 10.2147/TACG.S60472. eCollection 2015. Appl Clin Genet. 2015. PMID: 26124674 Free PMC article. Review.
202 results