Maisch B - Search Results

1

Novel mutations in the sarcomeric protein myopalladin in patients with dilated cardiomyopathy.

Meyer T, Ruppert V, Ackermann S, Richter A, Perrot A, Sperling SR, Posch MG, Maisch B, Pankuweit S; German Competence Network Heart Failure. Meyer T, et al. Among authors: maisch b. Eur J Hum Genet. 2013 Mar;21(3):294-300. doi: 10.1038/ejhg.2012.173. Epub 2012 Aug 15. Eur J Hum Genet. 2013. PMID: 22892539 Free PMC article.

2

Evidence for CTLA4 as a susceptibility gene for dilated cardiomyopathy.

Ruppert V, Meyer T, Struwe C, Petersen J, Perrot A, Posch MG, Ozcelik C, Richter A, Maisch B, Pankuweit S; German Heart Failure Network. Ruppert V, et al. Among authors: maisch b. Eur J Hum Genet. 2010 Jun;18(6):694-9. doi: 10.1038/ejhg.2010.3. Epub 2010 Feb 10. Eur J Hum Genet. 2010. PMID: 20145677 Free PMC article.

3

Identification of a missense mutation in the melusin-encoding ITGB1BP2 gene in a patient with dilated cardiomyopathy.

Ruppert V, Meyer T, Richter A, Maisch B, Pankuweit S; German Competence Network of Heart Failure. Ruppert V, et al. Among authors: maisch b. Gene. 2013 Jan 10;512(2):206-10. doi: 10.1016/j.gene.2012.10.055. Epub 2012 Nov 1. Gene. 2013. PMID: 23124043 Clinical Trial.

4

Detection of a large duplication mutation in the myosin-binding protein C3 gene in a case of hypertrophic cardiomyopathy.

Meyer T, Pankuweit S, Richter A, Maisch B, Ruppert V. Meyer T, et al. Among authors: maisch b. Gene. 2013 Sep 15;527(1):416-20. doi: 10.1016/j.gene.2013.06.025. Epub 2013 Jun 29. Gene. 2013. PMID: 23816408

5

Novel point mutations in the mitochondrial DNA detected in patients with dilated cardiomyopathy by screening the whole mitochondrial genome.

Ruppert V, Nolte D, Aschenbrenner T, Pankuweit S, Funck R, Maisch B. Ruppert V, et al. Among authors: maisch b. Biochem Biophys Res Commun. 2004 May 28;318(2):535-43. doi: 10.1016/j.bbrc.2004.04.061. Biochem Biophys Res Commun. 2004. PMID: 15120634

6

Inflammation in dilated cardiomyopathy.

Pankuweit S, Ruppert V, Maisch B. Pankuweit S, et al. Among authors: maisch b. Herz. 2004 Dec;29(8):788-93. doi: 10.1007/s00059-004-2626-9. Herz. 2004. PMID: 15599676 Review.

7

Inflammatory dilated cardiomyopathy (DCMI).

Maisch B, Richter A, Sandmöller A, Portig I, Pankuweit S; BMBF-Heart Failure Network. Maisch B, et al. Herz. 2005 Sep;30(6):535-44. doi: 10.1007/s00059-005-2730-5. Herz. 2005. PMID: 16170686 Review.

8

Familial inflammatory dilated cardiomyopathy.

Portig I, Wilke A, Freyland M, Wolf MJ, Richter A, Ruppert V, Pankuweit S, Maisch B. Portig I, et al. Among authors: maisch b. Eur J Heart Fail. 2006 Dec;8(8):816-25. doi: 10.1016/j.ejheart.2006.02.010. Epub 2006 Mar 6. Eur J Heart Fail. 2006. PMID: 16713338 Free article.

9

Mutations in MYOZ1 as well as MYOZ2 encoding the calsarcins are not associated with idiopathic and familial dilated cardiomyopathy.

Posch MG, Perrot A, Dietz R, Ozcelik C, Pankuweit S, Ruppert V, Richter A, Maisch B. Posch MG, et al. Among authors: maisch b. Mol Genet Metab. 2007 Jun;91(2):207-8. doi: 10.1016/j.ymgme.2007.02.014. Epub 2007 Apr 16. Mol Genet Metab. 2007. PMID: 17434779 No abstract available.

10

A missense variant in desmoglein-2 predisposes to dilated cardiomyopathy.

Posch MG, Posch MJ, Geier C, Erdmann B, Mueller W, Richter A, Ruppert V, Pankuweit S, Maisch B, Perrot A, Buttgereit J, Dietz R, Haverkamp W, Ozcelik C. Posch MG, et al. Among authors: maisch b. Mol Genet Metab. 2008 Sep-Oct;95(1-2):74-80. doi: 10.1016/j.ymgme.2008.06.005. Epub 2008 Aug 3. Mol Genet Metab. 2008. PMID: 18678517

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