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Prevalence of cardiac beta-myosin heavy chain gene mutations in patients with hypertrophic cardiomyopathy.
Perrot A, Schmidt-Traub H, Hoffmann B, Prager M, Bit-Avragim N, Rudenko RI, Usupbaeva DA, Kabaeva Z, Imanov B, Mirrakhimov MM, Dietz R, Wycisk A, Tendera M, Gessner R, Osterziel KJ. Perrot A, et al. Among authors: dietz r. J Mol Med (Berl). 2005 Jun;83(6):468-77. doi: 10.1007/s00109-005-0635-7. Epub 2005 Apr 22. J Mol Med (Berl). 2005. PMID: 15856146
Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy.
Geier C, Gehmlich K, Ehler E, Hassfeld S, Perrot A, Hayess K, Cardim N, Wenzel K, Erdmann B, Krackhardt F, Posch MG, Osterziel KJ, Bublak A, Nägele H, Scheffold T, Dietz R, Chien KR, Spuler S, Fürst DO, Nürnberg P, Ozcelik C. Geier C, et al. Among authors: dietz r. Hum Mol Genet. 2008 Sep 15;17(18):2753-65. doi: 10.1093/hmg/ddn160. Epub 2008 May 27. Hum Mol Genet. 2008. PMID: 18505755
Mutations in the human muscle LIM protein gene in families with hypertrophic cardiomyopathy.
Geier C, Perrot A, Ozcelik C, Binner P, Counsell D, Hoffmann K, Pilz B, Martiniak Y, Gehmlich K, van der Ven PF, Fürst DO, Vornwald A, von Hodenberg E, Nürnberg P, Scheffold T, Dietz R, Osterziel KJ. Geier C, et al. Among authors: dietz r. Circulation. 2003 Mar 18;107(10):1390-5. doi: 10.1161/01.cir.0000056522.82563.5f. Circulation. 2003. PMID: 12642359
Genetic and phenotypic analysis of dilated cardiomyopathy with conduction system disease: demand for strategies in the management of presymptomatic lamin A/C mutant carriers.
Perrot A, Sigusch HH, Nägele H, Genschel J, Lehmkuhl H, Hetzer R, Geier C, Leon Perez V, Reinhard D, Dietz R, Josef Osterziel K, Schmidt HH. Perrot A, et al. Among authors: dietz r. Eur J Heart Fail. 2006 Aug;8(5):484-93. doi: 10.1016/j.ejheart.2005.11.004. Epub 2006 Jan 4. Eur J Heart Fail. 2006. PMID: 16386954 Free article.
914 results