Matrix remodelling in dilated cardiomyopathy entails the occurrence of oncofetal fibronectin molecular variants.

Author:

Gabler U.,Berndt A.,Kosmehl H.,Mandel U.,Zardi L.,Muller S.,Stelzner A.,Katenkamp D.

Publisher

BMJ

Subject

Cardiology and Cardiovascular Medicine

Reference46 articles.

1. The challenge of cardiomyopathy;Abelmann, W.H.; Lorell, B.H.;Am Coll Cardiol,1989

2. The causes of dilated cardiomyopathy: a clinicopathologic review of 673 consecutive patients;Kasper, E.K.; Agema, W.R.P.; Hutchins, G.M.; Deckers, J.W.; Gabler, Berndt; Kosmehl, Mandel; Zardi, Maller;JAm Coll Cardiol,1994

3. Idiopathic dilated cardiomyopathy: analysis of 152 necropsy patients;Roberts, W.C.; Siegel, R.J.; McManus, B.M.;Am J Cardiol,1987

4. The morphologic spectrum of dilated cardiomyopathy and its relation to immune-response genes;Arbustini, E.; Gavazzi, A.; Pozzi, R.;Am J Cardiol,1989

5. Experimental induced murine rhabdomyosarcoma-correlation between cellular contacts, matrix formation and cellular differentiation;Langbein, L.; Kosmehl, H.; Katenkamp, D.; Neupert, G.; Stiller, K.-J.;Differentiation,1990

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