Amyloid heart disease is the most frequent type of cardiomyopathy with restrictive physiology in Western countries. It is a complex entity with very varied pathophyiology. Even though a definitive diagnosis can readily be made from histological findings in involved tissues, amyloid heart disease is still frequently under diagnosed

Rapezzi C, Quarta CC, Riva L, Salvi F, Ciliberti P, Longhi S, et al. (2010). Familial Amyloidoses and the Heart. NEW YORK : Oxford University Press.

Familial Amyloidoses and the Heart

RAPEZZI, CLAUDIO;QUARTA, CANDIDA CRISTINA;RIVA, LETIZIA;SALVI, FABRIZIO;CILIBERTI, PAOLO;LONGHI, SIMONE;BIAGINI, ELENA;PERUGINI, ENRICA
2010

Abstract

Amyloid heart disease is the most frequent type of cardiomyopathy with restrictive physiology in Western countries. It is a complex entity with very varied pathophyiology. Even though a definitive diagnosis can readily be made from histological findings in involved tissues, amyloid heart disease is still frequently under diagnosed
2010
Principles and practice of Clinical Cardiovascular Genetics
441
458
Rapezzi C, Quarta CC, Riva L, Salvi F, Ciliberti P, Longhi S, et al. (2010). Familial Amyloidoses and the Heart. NEW YORK : Oxford University Press.
Rapezzi C; Quarta CC; Riva L; Salvi F; Ciliberti P; Longhi S; Biagini E; Perugini E.
File in questo prodotto:
Eventuali allegati, non sono esposti

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/89115
 Attenzione

Attenzione! I dati visualizzati non sono stati sottoposti a validazione da parte dell'ateneo

Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus ND
  • ???jsp.display-item.citation.isi??? ND
social impact