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

Year Number of Results
1991 1
1992 2
1993 1
1994 1
1996 1
1998 1
2001 5
2002 1
2004 1
2007 1
2010 2
2011 6
2012 3
2013 6
2014 4
2015 4
2017 4
2018 4
2019 8
2020 7
2021 8
2022 6
2023 5
2024 1

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72 results

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Page 1
Clinical findings associated with incomplete hemodynamic left ventricular unloading in patients with a left ventricular assist device.
Ruiz-Cano MJ, Schramm R, Paluszkiewicz L, Ramazyan L, Rojas SV, Lauenroth V, Krenz A, Gummert J, Morshuis M. Ruiz-Cano MJ, et al. Among authors: paluszkiewicz l. Rev Esp Cardiol (Engl Ed). 2022 Aug;75(8):626-635. doi: 10.1016/j.rec.2021.06.012. Epub 2021 Jul 22. Rev Esp Cardiol (Engl Ed). 2022. PMID: 34303643 English, Spanish.
A homozygous DSC2 deletion associated with arrhythmogenic cardiomyopathy is caused by uniparental isodisomy.
Brodehl A, Weiss J, Debus JD, Stanasiuk C, Klauke B, Deutsch MA, Fox H, Bax J, Ebbinghaus H, Gärtner A, Tiesmeier J, Laser T, Peterschröder A, Gerull B, Gummert J, Paluszkiewicz L, Milting H. Brodehl A, et al. Among authors: paluszkiewicz l. J Mol Cell Cardiol. 2020 Apr;141:17-29. doi: 10.1016/j.yjmcc.2020.03.006. Epub 2020 Mar 19. J Mol Cell Cardiol. 2020. PMID: 32201174 Free article.
The novel αB-crystallin (CRYAB) mutation p.D109G causes restrictive cardiomyopathy.
Brodehl A, Gaertner-Rommel A, Klauke B, Grewe SA, Schirmer I, Peterschröder A, Faber L, Vorgerd M, Gummert J, Anselmetti D, Schulz U, Paluszkiewicz L, Milting H. Brodehl A, et al. Among authors: paluszkiewicz l. Hum Mutat. 2017 Aug;38(8):947-952. doi: 10.1002/humu.23248. Epub 2017 Jun 21. Hum Mutat. 2017. PMID: 28493373
72 results