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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2004 1
2005 2
2007 2
2009 1
2012 1
2013 1
2016 1
2017 1
2018 2
2019 3
2022 1
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16 results

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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: seidel h. J Clin Med. 2019 Nov 29;8(12):2079. doi: 10.3390/jcm8122079. J Clin Med. 2019. PMID: 31795342 Free PMC article.
Long-term outcomes of childhood onset Noonan compared to sarcomere hypertrophic cardiomyopathy.
Kaltenecker E, Schleihauf J, Meierhofer C, Shehu N, Mkrtchyan N, Hager A, Kühn A, Cleuziou J, Klingel K, Seidel H, Zenker M, Ewert P, Hessling G, Wolf CM. Kaltenecker E, et al. Among authors: seidel h. Cardiovasc Diagn Ther. 2019 Oct;9(Suppl 2):S299-S309. doi: 10.21037/cdt.2019.05.01. Cardiovasc Diagn Ther. 2019. PMID: 31737538 Free PMC article.
Hemostatic abnormalities in adult patients with Marfan syndrome.
Kornhuber KTI, Seidel H, Pujol C, Meierhofer C, Röschenthaler F, Pressler A, Stöckl A, Nagdyman N, Neidenbach RC, von Hundelshausen P, Halle M, Holdenrieder S, Ewert P, Kaemmerer H, Hauser M. Kornhuber KTI, et al. Among authors: seidel h. Cardiovasc Diagn Ther. 2019 Oct;9(Suppl 2):S209-S220. doi: 10.21037/cdt.2019.08.09. Cardiovasc Diagn Ther. 2019. PMID: 31737529 Free PMC article.
Corrigendum to: 'Clinical long-term outcome of septal myectomy for obstructive hypertrophic cardiomyopathy in infants' [Eur J Cardiothorac Surg 2018;53:538--44].
Schleihauf J, Cleuziou J, Pabst von Ohain J, Meierhofer C, Stern H, Shehu N, Mkrtchyan N, Kaltenecker E, Kühn A, Nagdyman N, Hager A, Seidel H, Lange R, Ewert P, Wolf CM. Schleihauf J, et al. Among authors: seidel h. Eur J Cardiothorac Surg. 2018 Mar 1;53(3):694. doi: 10.1093/ejcts/ezx441. Eur J Cardiothorac Surg. 2018. PMID: 29211880 No abstract available.
Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation.
Kouz K, Lissewski C, Spranger S, Mitter D, Riess A, Lopez-Gonzalez V, Lüttgen S, Aydin H, von Deimling F, Evers C, Hahn A, Hempel M, Issa U, Kahlert AK, Lieb A, Villavicencio-Lorini P, Ballesta-Martinez MJ, Nampoothiri S, Ovens-Raeder A, Puchmajerová A, Satanovskij R, Seidel H, Unkelbach S, Zabel B, Kutsche K, Zenker M. Kouz K, et al. Among authors: seidel h. Genet Med. 2016 Dec;18(12):1226-1234. doi: 10.1038/gim.2016.32. Epub 2016 Apr 21. Genet Med. 2016. PMID: 27101134 Free article.
16 results