Familial dilated cardiomyopathy.

نویسندگان

  • L Mestroni
  • M Krajinovic
  • G M Severini
  • B Pinamonti
  • A Di Lenarda
  • M Giacca
  • A Falaschi
  • F Camerini
چکیده

We are delighted to announce that Circulation is now receiving manuscripts and reviews electronically. We had attempted to avail our readers and supporters of an online system more than two years ago, but the existing systems were not sufficient to handle the large volume of manuscripts that we were receiving and reviewing at Circulation. We are pleased that with the advancement of technology, we can now make available to our readership the ease of electronic submission of manuscripts via Bench Press. Manuscripts will be reviewed and decisions communicated to authors electronically as well. We believe that this represents a step forward in expediting Circulation’s workflow as we receive and review manuscripts and communicate with authors. We hope that the system will be widely used. Please let us know your suggestions for improving our efforts.

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Idiopathic dilated cardiomyopathy: familial prevalence and HLA distribution.

OBJECTIVES To compare HLA distribution in familial and non-familial dilated cardiomyopathy, because a serum marker that could identify families at risk of developing dilated cardiomyopathy should be of use in screening for the disease. PATIENTS 100 patients with dilated cardiomyopathy. METHODS 200 first degree relatives from 56 of the proband families were screened for dilated cardiomyopath...

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Clinical and genetic issues in familial dilated cardiomyopathy.

Idiopathic dilated cardiomyopathy (IDC) is characterized by left ventricular dilatation and systolic dysfunction after known causes have been excluded. Idiopathic dilated cardiomyopathy occurring in families, or familial dilated cardiomyopathy (FDC), may occur in 20% to 50% of IDC cases. Sixteen genes have been shown to cause autosomal dominant FDC, but collectively may account for only a fract...

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Histopathology of Familial Versus Nonfamilial Dilated Cardiomyopathy

Idiopathic dilated cardiomyopathy is most likely a heterogenous group of diseases characterized by ventricular dilatation and dysfunction. Approximately 20% of patients with idiopathic dilated cardiomyopathy have familial disease, which may be inapparent by review of the family history alone. It has been suggested that histopathologic features, particularly the presence of bizarrely shaped mito...

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Familial dilated (congestive) cardiomyopathy. Occurrence in two brothers and an overview of the literature.

Two young White brothers had dilated (congestive) cardiomyopathy. The elder came to autopsy after a chronic course of congestive cardiac failure, the younger underwent repeated cardiac catheterization and transvenous right ventricular endomyocardial biopsy specimens demonstrated histopathological features in keeping with a diagnosis of idiopathic dilated cardiomyopathy. These brothers may have ...

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CARDIOVASCULAR MEDICINE Progression of familial and non-familial dilated cardiomyopathy: long term follow up

Background: It is unknown whether progression of familial idiopathic dilated cardiomyopathy differs from progression in the non-familial form. It has been suggested that familial disease indicates a worse prognosis, and that this should be considered when planning the timing of heart transplantation. Objective: To compare five year survival or time to heart transplantation in an unselected seri...

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Progression of familial and non-familial dilated cardiomyopathy: long term follow up.

BACKGROUND It is unknown whether progression of familial idiopathic dilated cardiomyopathy differs from progression in the non-familial form. It has been suggested that familial disease indicates a worse prognosis, and that this should be considered when planning the timing of heart transplantation. OBJECTIVE To compare five year survival or time to heart transplantation in an unselected seri...

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عنوان ژورنال:
  • British heart journal

دوره 72 6 Suppl  شماره 

صفحات  -

تاریخ انتشار 1994