Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

793 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Case-matched Comparison of Cardiovascular Outcome in Loeys-Dietz Syndrome versus Marfan Syndrome.
Mühlstädt K, De Backer J, von Kodolitsch Y, Kutsche K, Muiño Mosquera L, Brickwedel J, Girdauskas E, Mir TS, Mahlmann A, Tsilimparis N, Staebler A, Schoof L, Seidel H, Berger J, Bernhardt AM, Blankenberg S, Kölbel T, Detter C, Szöcs K, Kaemmerer H. Mühlstädt K, et al. Among authors: blankenberg s. J Clin Med. 2019 Nov 29;8(12):2079. doi: 10.3390/jcm8122079. J Clin Med. 2019. PMID: 31795342 Free PMC article.
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: blankenberg s. 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: blankenberg s. 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: blankenberg s. 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: blankenberg s. PLoS One. 2013 Dec 13;8(12):e81281. doi: 10.1371/journal.pone.0081281. eCollection 2013. PLoS One. 2013. PMID: 24349050 Free PMC article.
Myeloperoxidase upregulates endothelin receptor type B expression.
Lau D, Szöcs K, Klinke A, Rudolph T, Rudolph V, Streichert T, Blankenberg S, Baldus S. Lau D, et al. Among authors: blankenberg s. J Mol Cell Cardiol. 2014 Apr;69:76-82. doi: 10.1016/j.yjmcc.2013.12.007. Epub 2014 Jan 10. J Mol Cell Cardiol. 2014. PMID: 24417960
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: blankenberg s. 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: blankenberg s. 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. Among authors: blankenberg s. 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.
793 results