Genetic and phenotypic analysis of dilated cardiomyopathy with conduction system disease: demand for strategies in the management of presymptomatic lamin A/C mutant carriers. (Q52935374)

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scientific article published on 4 January 2006

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English	Genetic and phenotypic analysis of dilated cardiomyopathy with conduction system disease: demand for strategies in the management of presymptomatic lamin A/C mutant carriers.	scientific article published on 4 January 2006

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15 January 2020

Genetic and phenotypic analysis of dilated cardiomyopathy with conduction system disease: demand for strategies in the management of presymptomatic lamin A/C mutant carriers (English)

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Europe PubMed Central

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15 January 2020

dilated cardiomyopathy

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Holger H Sigusch

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15 January 2020

Herbert Nägele

3

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15 January 2020

Janine Genschel

4

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15 January 2020

Hans Lehmkuhl

5

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15 January 2020

Christian Geier

7

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15 January 2020

Veronica Leon Perez

8

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15 January 2020

Dirk Reinhard

9

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15 January 2020

Rainer Dietz

10

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15 January 2020

Karl Josef Osterziel

11

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15 January 2020

Hartmut H-J Schmidt

12

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15 January 2020

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4 January 2006

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15 January 2020

European Journal of Heart Failure

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15 January 2020

8

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15 January 2020

5

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15 January 2020

484-493

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15 January 2020

The Frequency of Familial Dilated Cardiomyopathy in a Series of Patients with Idiopathic Dilated Cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FJ.EJHEART.2005.11.004

21 January 2018

Familial dilated cardiomyopathy in the United Kingdom

1 reference

https://api.crossref.org/works/10.1016%2FJ.EJHEART.2005.11.004

21 January 2018

Frequency and phenotypes of familial dilated cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1016%2FJ.EJHEART.2005.11.004

21 January 2018

The Genetic Basis for Cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FJ.EJHEART.2005.11.004

21 January 2018

Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease

1 reference

https://api.crossref.org/works/10.1016%2FJ.EJHEART.2005.11.004

21 January 2018

LMNA mutations in cardiac transplant recipients.

1 reference

https://api.crossref.org/works/10.1016%2FJ.EJHEART.2005.11.004

21 January 2018

Lamins: building blocks or regulators of gene expression?

1 reference

https://api.crossref.org/works/10.1016%2FJ.EJHEART.2005.11.004

21 January 2018

Laminopathies: from the heart of the cell to the clinics

1 reference

https://api.crossref.org/works/10.1016%2FJ.EJHEART.2005.11.004

21 January 2018

Echocardiographic measurements in normal subjects from infancy to old age.

1 reference

https://api.crossref.org/works/10.1016%2FJ.EJHEART.2005.11.004

21 January 2018

Distribution and categorization of echocardiographic measurements in relation to reference limits: the Framingham Heart Study: formulation of a height- and sex-specific classification and its prospective validation

1 reference

https://api.crossref.org/works/10.1016%2FJ.EJHEART.2005.11.004

21 January 2018

Guidelines for the study of familial dilated cardiomyopathies. Collaborative Research Group of the European Human and Capital Mobility Project on Familial Dilated Cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1016%2FJ.EJHEART.2005.11.004

21 January 2018

Autosomal dominant dilated cardiomyopathy with atrioventricular block: a lamin A/C defect-related disease

1 reference

https://api.crossref.org/works/10.1016%2FJ.EJHEART.2005.11.004

21 January 2018

Loss of lamin A/C expression revealed by immuno-electron microscopy in dilated cardiomyopathy with atrioventricular block caused by LMNA gene defects.

1 reference

https://api.crossref.org/works/10.1016%2FJ.EJHEART.2005.11.004

21 January 2018

Defects in nuclear structure and function promote dilated cardiomyopathy in lamin A/C-deficient mice

1 reference

https://api.crossref.org/works/10.1016%2FJ.EJHEART.2005.11.004

21 January 2018

How do mutations in lamins A and C cause disease?

1 reference

https://api.crossref.org/works/10.1016%2FJ.EJHEART.2005.11.004

21 January 2018

Functional consequences of an LMNA mutation associated with a new cardiac and non-cardiac phenotype

1 reference

https://api.crossref.org/works/10.1016%2FJ.EJHEART.2005.11.004

21 January 2018

Idiopathic Dilated Cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FJ.EJHEART.2005.11.004

21 January 2018

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