(Q83426303)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21327842%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

title

Sudden cardiac death in a patient with lamin A/C mutation in the absence of dilated cardiomyopathy or conduction disease (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21327842%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

main subject

dilated cardiomyopathy

1 reference

5

Martin Borggrefe

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21327842%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

7

Rainer Schimpf

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21327842%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

3

Theano Papavassiliu

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21327842%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

6

Hugo A Katus

1 reference

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22 January 2020

4

Benjamin Meder

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21327842%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

author name string

Philipp Ehlermann

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21327842%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

Stephanie Lehrke

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21327842%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

publication date

16 February 2011

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21327842%20AND%20SRC:MED&resulttype=core&format=json

Clinical Research in Cardiology

22 January 2020

published in

1 reference

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22 January 2020

volume

100

1 reference

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22 January 2020

issue

6

1 reference

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22 January 2020

page(s)

547-551

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21327842%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s00392-011-0289-0

22 January 2020

exact match

0 references

cites work

Malignant mutation in the lamin A/C gene causing progressive conduction system disease and early sudden death in a family with mild form of limb-girdle muscular dystrophy

1 reference

12 December 2020

Lamin A/C truncation in dilated cardiomyopathy with conduction disease

1 reference

12 December 2020

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

1 reference

12 December 2020

Laminopathy presenting as familial atrial fibrillation

1 reference

12 December 2020

Natural history of dilated cardiomyopathy due to lamin A/C gene mutations

1 reference

12 December 2020

Images in cardiovascular medicine. Cardiomyopathy in a Duchenne muscular dystrophy carrier and her diseased son: similar pattern revealed by cardiovascular MRI

1 reference

12 December 2020

Clinical and genetic issues in familial dilated cardiomyopathy

1 reference

12 December 2020

Long-Term Outcome and Risk Stratification in Dilated Cardiolaminopathies

1 reference

12 December 2020

Frequency and phenotypes of familial dilated cardiomyopathy.

1 reference

12 December 2020

Differentiation of heart failure related to dilated cardiomyopathy and coronary artery disease using gadolinium-enhanced cardiovascular magnetic resonance

1 reference

12 December 2020

Myocardial delayed enhancement by magnetic resonance imaging in patients with muscular dystrophy

1 reference

12 December 2020

Genetic and ultrastructural studies in dilated cardiomyopathy patients: a large deletion in the lamin A/C gene is associated with cardiomyocyte nuclear envelope disruption

1 reference

12 December 2020

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

1 reference

12 December 2020

Human laminopathies: nuclei gone genetically awry

1 reference

12 December 2020

Clinical characteristics of sudden death victims in heritable (chromosome 1p1-1q1) conduction and myocardial disease

1 reference

12 December 2020

Primary prevention of sudden death in patients with lamin A/C gene mutations.

1 reference

12 December 2020

Identification of mutational hot spots in LMNA encoding lamin A/C in patients with familial dilated cardiomyopathy

1 reference

12 December 2020

Meta-analysis of clinical characteristics of 299 carriers of LMNA gene mutations: do lamin A/C mutations portend a high risk of sudden death?

1 reference

12 December 2020

Familial cardiomyopathy: Autosomally, dominantiy inherited congestive cardiomyopathy with two cases of septal hypertrophy in one family

1 reference

12 December 2020

In vivo and in vitro examination of the functional significances of novel lamin gene mutations in heart failure patients

1 reference

12 December 2020

Delayed enhancement cardiovascular magnetic resonance assessment of non-ischaemic cardiomyopathies

1 reference

12 December 2020

Late gadolinium enhanced cardiovascular magnetic resonance in Becker muscular dystrophy

1 reference

12 December 2020

Reviews of translational medicine and genomics in cardiovascular disease: new disease taxonomy and therapeutic implications cardiomyopathies: therapeutics based on molecular phenotype

1 reference

12 December 2020

A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1

1 reference

12 December 2020

Evolution of a hereditary cardiac conduction and muscle disorder: a study involving a family with six generations affected

1 reference

12 December 2020

Mid-myocardial fibrosis by cardiac magnetic resonance in patients with lamin A/C cardiomyopathy: possible substrate for diastolic dysfunction

1 reference

12 December 2020

Late gadolinium enhancement by cardiovascular magnetic resonance heralds an adverse prognosis in nonischemic cardiomyopathy

1 reference

12 December 2020

Lamin A/C and cardiac diseases

1 reference

12 December 2020

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

1 reference

12 December 2020

Familial dilated cardiomyopathy

1 reference

12 December 2020

10.1007/S00392-011-0289-0

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21327842%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

1 reference