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(30) Annibale, Paolo Dr. (3) Bader, Michael Prof. Dr. (93) Bähring, Sylvia Dr. (4) Bartolomaeus, Hendrik (3) Baumann, Elisabeth (1) Begay-Müller, Valerie Dr. (2) Bernert, Carola (1) Beule, Dieter Dr. (7) Birchmeier, Walter Prof. Dr. (22) Birchmeier-Kohler, Carmen Prof. Dr. (16) Birol, Melissa Dr. (1) Blachut, Susanne (2) Blankenstein, Thomas Prof. Dr. (19) Blume, Alexander Dr. (1) Bock-Bierbaum, Tobias Dr. (2) Borodina, Tatiana Dr. (1) Braeuning, Caroline (1) Cakmak-Görür, Nese Dr. (1) Cano Rincon, Elena Dr. (1) Castilho de Barros, Carlos Prof. Dr. (1) Chekulaeva, Marina Dr. (4) Chen, Wei Prof. Dr. (18) Chu, Van Trung Dr. (6) Conrad, Thomas Dr. (1) Coralluzzo, Violeta (1) Coscia, Fabian Dr. (3) Dahlmann, Mathias Dr. (2) Daniel, Peter Prof. Dr. (7) Dartsch, Josephine (3) Daumke, Oliver Prof. Dr. (12) Dechend, Ralf Priv. Doz. 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(6) Luft, Friedrich Prof. Dr. (118) Luganskaja, Tatjana (1) Lupianez Garcia, Dario Jesus Dr. (2) Maatz, Henrike Dr. (2) Maglione, Marta (3) Mahmoodzadeh, Shokoufeh PD Dr. (2) Mais, Lisa (1) Malchin, Victoria (1) Marenholz, Ingo Dr. (2) Marg, Andreas Dr. (2) Marko, Lajos Dr. (10) Mastrobuoni, Guido Dr. (2) Mathas, Stephan Dr. (8) Meier, Katja (1) Merks, Anne Margarete Dr. (1) Mertins, Philipp Dr. (8) Metzger, Jakob Johannes Dr. (2) Meyer, Irmtraud Margret Prof. Dr. (10) Migueles Lozano, Oscar Arturo Dr. (1) Millward, Jason Dr. (2) Mittnenzweig, Markus Dr. (1) Morano, Ingo Prof. Dr. (9) Müller, Dominik Prof. Dr. (39) Müller, Gerd Dr. (1) Müller, Marion (1) Müller, Thomas Dr. (2) Müthel, Stefanie (2) Na, Il-Kang Dr. (7) Nazare, Marc (5) Neubert, Wilhelm (1) Neuendorf, Nancy (1) Nguyen, Tam Hoai Dr. (1) Niendorf, Thoralf Prof. Dr. (27) Nimptsch, Katharina Dr. (6) Noel, Jeffrey Dr. (4) Nolte, Christiane Dr. (7) Obermayer-Wasserscheid, Benedikt Dr. (1) Oertel, Frederike Cosima MD/PhD (5) Ofenbauer, Andreas Dr. (3) Ohler, Uwe Prof. Dr. (8) Patone, Giannino Dr. (5) Paul, Friedemann Prof. Dr. med. 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Januar 2004 / J Med Genet Clinical and genetic characteristics of a cardiac actin gene mutations in hypertrophic cardiomyopathy J. Mogensen A. Perrot P.S. Andersen O. Havndrup I.C. Klausen M. Christiansen P. Bross H. Egeblad H. Bundgaard K.J. Osterziel G. Haltern H. Lapp P. Reinecke N. Gregersen A.D. Borglum 15. Mai 2004 / Am J Med Effects of ACE gene insertion/deletion polymorphism on response to spironolactone in patients with chronic heart failure M. Cicoira A. Rossi S. Bonapace L. Zanolla A. Perrot D.P. Francis G. Golia L. Franceschini K.J. Osterziel P. Zardini 15. Januar 2008 / Am J Med Genet A Mutations in GATA4, NKX2.5, CRELD1, and BMP4 are infrequently found in patients with congenital cardiac septal defects M.G. Posch A. Perrot K. Schmitt S. Mittelhaus E.M. Esenwein B. Stiller C. Geier R. Dietz R. Gessner C. Oezcelik F. Berger 24. April 2008 / Oncogene Common tumour p53 mutations in immortalized cells from Hupki mice heterozygous at codon 72 M. Reinbold J.L. Luo T. Nedelko B. Jerchow M.E. Murphy C. Whibley Q. Wei M. Hollstein 01. Januar 2008 / Dis Markers Mitochondrial transcription factors TFA, TFB1 and TFB2: A search for DNA variants/haplotypes and the risk of cardiac hypertrophy C. Alonso-Montes M.G. Castro J.R. Reguero A. Perrot C. Oezcelik C. Geier M.G. Posch C. Moris V. Alvarez M. Ruiz-Ortega E. Coto 01. Juli 2008 / Med Sci Monit Sequence analysis of myozenin 2 in 438 European patients with familial hypertrophic cardiomyopathy M.G. Posch L. Thiemann P. Tomasov J. Veselka N. Cardim M. Garcia-Castro E. Coto A. Perrot C. Geier R. Dietz W. Haverkamp C. Oezcelik 01. September 2008 / Mol Genet Metab A missense variant in desmoglein-2 predisposes to dilated cardiomyopathy M.G. Posch M.J. Posch C. Geier B. Erdmann W. Mueller A. Richter V. Ruppert S. Pankuweit B. Maisch A. Perrot J. Buttgereit R. Dietz W. Haverkamp C. Oezcelik 01. Mai 2008 / J Med Genet We need a detailed phenome in the phenomenon of genetics and congenital heart disease M.G. Posch F. Berger A. Perrot C. Oezcelik 15. September 2008 / Hum Mol Genet Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy C. Geier K. Gehmlich E. Ehler S. Hassfeld A. Perrot K. Hayess N. Cardim K. Wenzel B. Erdmann F. Krackhardt M.G. Posch A. Bublak H. Naegele T. Scheffold R. Dietz K.R. Chien S. Spuler D.O. Fuerst P. Nuernberg C. Oezcelik 01. Dezember 2008 / Nat Clin Pract Cardiovasc Med Variations in DSG2: V56M, V158G and V920G are not pathogenic for arrhythmogenic right ventricular dysplasia/cardiomyopathy M.G. Posch M.J. Posch A. Perrot R. Dietz C. Oezcelik Seitennummerierung Aktuelle Seite 1 Seite 2 Seite 3 Nächste Seite Next › Letzte Seite Last »
01. Januar 2004 / J Med Genet Clinical and genetic characteristics of a cardiac actin gene mutations in hypertrophic cardiomyopathy J. Mogensen A. Perrot P.S. Andersen O. Havndrup I.C. Klausen M. Christiansen P. Bross H. Egeblad H. Bundgaard K.J. Osterziel G. Haltern H. Lapp P. Reinecke N. Gregersen A.D. Borglum
15. Mai 2004 / Am J Med Effects of ACE gene insertion/deletion polymorphism on response to spironolactone in patients with chronic heart failure M. Cicoira A. Rossi S. Bonapace L. Zanolla A. Perrot D.P. Francis G. Golia L. Franceschini K.J. Osterziel P. Zardini
15. Januar 2008 / Am J Med Genet A Mutations in GATA4, NKX2.5, CRELD1, and BMP4 are infrequently found in patients with congenital cardiac septal defects M.G. Posch A. Perrot K. Schmitt S. Mittelhaus E.M. Esenwein B. Stiller C. Geier R. Dietz R. Gessner C. Oezcelik F. Berger
24. April 2008 / Oncogene Common tumour p53 mutations in immortalized cells from Hupki mice heterozygous at codon 72 M. Reinbold J.L. Luo T. Nedelko B. Jerchow M.E. Murphy C. Whibley Q. Wei M. Hollstein
01. Januar 2008 / Dis Markers Mitochondrial transcription factors TFA, TFB1 and TFB2: A search for DNA variants/haplotypes and the risk of cardiac hypertrophy C. Alonso-Montes M.G. Castro J.R. Reguero A. Perrot C. Oezcelik C. Geier M.G. Posch C. Moris V. Alvarez M. Ruiz-Ortega E. Coto
01. Juli 2008 / Med Sci Monit Sequence analysis of myozenin 2 in 438 European patients with familial hypertrophic cardiomyopathy M.G. Posch L. Thiemann P. Tomasov J. Veselka N. Cardim M. Garcia-Castro E. Coto A. Perrot C. Geier R. Dietz W. Haverkamp C. Oezcelik
01. September 2008 / Mol Genet Metab A missense variant in desmoglein-2 predisposes to dilated cardiomyopathy M.G. Posch M.J. Posch C. Geier B. Erdmann W. Mueller A. Richter V. Ruppert S. Pankuweit B. Maisch A. Perrot J. Buttgereit R. Dietz W. Haverkamp C. Oezcelik
01. Mai 2008 / J Med Genet We need a detailed phenome in the phenomenon of genetics and congenital heart disease M.G. Posch F. Berger A. Perrot C. Oezcelik
15. September 2008 / Hum Mol Genet Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy C. Geier K. Gehmlich E. Ehler S. Hassfeld A. Perrot K. Hayess N. Cardim K. Wenzel B. Erdmann F. Krackhardt M.G. Posch A. Bublak H. Naegele T. Scheffold R. Dietz K.R. Chien S. Spuler D.O. Fuerst P. Nuernberg C. Oezcelik
01. Dezember 2008 / Nat Clin Pract Cardiovasc Med Variations in DSG2: V56M, V158G and V920G are not pathogenic for arrhythmogenic right ventricular dysplasia/cardiomyopathy M.G. Posch M.J. Posch A. Perrot R. Dietz C. Oezcelik