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

98 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Blood-based microRNA signatures differentiate various forms of cardiac hypertrophy.
Derda AA, Thum S, Lorenzen JM, Bavendiek U, Heineke J, Keyser B, Stuhrmann M, Givens RC, Kennel PJ, Schulze PC, Widder JD, Bauersachs J, Thum T. Derda AA, et al. Among authors: keyser b. Int J Cardiol. 2015 Oct 1;196:115-22. doi: 10.1016/j.ijcard.2015.05.185. Epub 2015 Jun 5. Int J Cardiol. 2015. PMID: 26086795 Free PMC article.
High-density oligonucleotide-based resequencing assay for mutations causing syndromic and non-syndromic forms of thoracic aortic aneurysms and dissections.
Kathiravel U, Keyser B, Hoffjan S, Kötting J, Müller M, Sivalingam S, Bonin M, Arslan-Kirchner M, von Kodolitsch Y, Binner P, Scheffold T, Stuhrmann M, Waldmüller S. Kathiravel U, et al. Among authors: keyser b. Mol Cell Probes. 2013 Apr;27(2):103-8. doi: 10.1016/j.mcp.2012.10.002. Epub 2012 Nov 6. Mol Cell Probes. 2013. PMID: 23142374
Intrinsic MYH7 expression regulation contributes to tissue level allelic imbalance in hypertrophic cardiomyopathy.
Montag J, Syring M, Rose J, Weber AL, Ernstberger P, Mayer AK, Becker E, Keyser B, Dos Remedios C, Perrot A, van der Velden J, Francino A, Navarro-Lopez F, Ho CY, Brenner B, Kraft T. Montag J, et al. Among authors: keyser b. J Muscle Res Cell Motil. 2017 Aug;38(3-4):291-302. doi: 10.1007/s10974-017-9486-4. Epub 2017 Nov 3. J Muscle Res Cell Motil. 2017. PMID: 29101517 Free PMC article.
FBN1 gene mutation characteristics and clinical features for the prediction of mitral valve disease progression.
Kühne K, Keyser B, Groene EF, Sheikhzadeh S, Detter C, Lorenzen V, Hillebrand M, Bernhardt AM, Hoffmann B, Mir TS, Robinson PN, Berger J, Reichenspurner H, von Kodolitsch Y, Rybczynski M. Kühne K, et al. Among authors: keyser b. Int J Cardiol. 2013 Sep 30;168(2):953-9. doi: 10.1016/j.ijcard.2012.10.044. Epub 2012 Nov 22. Int J Cardiol. 2013. PMID: 23176764
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: keyser b. 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
Mitral valve prolapse syndrome and MASS phenotype: Stability of aortic dilatation but progression of mitral valve prolapse.
Rippe M, De Backer J, Kutsche K, Mosquera LM, Schüler H, Rybczynski M, Bernhardt AM, Keyser B, Hillebrand M, Mir TS, Berger J, Blankenberg S, Koschyk D, von Kodolitsch Y. Rippe M, et al. Among authors: keyser b. Int J Cardiol Heart Vasc. 2016 Jan 21;10:39-46. doi: 10.1016/j.ijcha.2016.01.002. eCollection 2016 Mar. Int J Cardiol Heart Vasc. 2016. PMID: 28616514 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: keyser b. 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.
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: keyser b. PLoS One. 2013 Dec 13;8(12):e81281. doi: 10.1371/journal.pone.0081281. eCollection 2013. PLoS One. 2013. PMID: 24349050 Free PMC article.
98 results