(Q83568905)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22388920%20AND%20SRC:MED&resulttype=core&format=json

24 January 2020

title

[Clinical and genetic aspects of hypertrophic and dilated cardiomyopathy] (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22388920%20AND%20SRC:MED&resulttype=core&format=json

24 January 2020

main subject

dilated cardiomyopathy

1 reference

2

H A Katus

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22388920%20AND%20SRC:MED&resulttype=core&format=json

24 January 2020

author name string

B Meder

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22388920%20AND%20SRC:MED&resulttype=core&format=json

24 January 2020

publication date

1 April 2012

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22388920%20AND%20SRC:MED&resulttype=core&format=json

24 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22388920%20AND%20SRC:MED&resulttype=core&format=json

24 January 2020

volume

53

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22388920%20AND%20SRC:MED&resulttype=core&format=json

24 January 2020

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22388920%20AND%20SRC:MED&resulttype=core&format=json

24 January 2020

page(s)

408-14, 417-8

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22388920%20AND%20SRC:MED&resulttype=core&format=json

Hypertrophic cardiomyopathy

24 January 2020

cites work

1 reference

12 December 2020

Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy

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12 December 2020

1 reference

12 December 2020

Prognostic role of high-sensitivity cardiac troponin T in patients with nonischemic dilated cardiomyopathy

1 reference

12 December 2020

Mechanisms of disease: hypertrophic cardiomyopathy

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12 December 2020

Prognostic impact of familial screening in dilated cardiomyopathy

1 reference

12 December 2020

Genetics of dilated cardiomyopathy

1 reference

12 December 2020

Genetic testing for potentially lethal, highly treatable inherited cardiomyopathies/channelopathies in clinical practice

1 reference

12 December 2020

Long-Term Outcome and Risk Stratification in Dilated Cardiolaminopathies

1 reference

12 December 2020

HBEGF, SRA1, and IK: Three cosegregating genes as determinants of cardiomyopathy

1 reference

12 December 2020

Safety and efficacy of recombinant human alpha-galactosidase A replacement therapy in Fabry's disease

1 reference

12 December 2020

Pharmacological inhibition of c-Jun N-terminal kinase signaling prevents cardiomyopathy caused by mutation in LMNA gene

1 reference

12 December 2020

Genome-based prediction of common diseases: advances and prospects

1 reference

12 December 2020

Prevalence of Anderson-Fabry disease in patients with hypertrophic cardiomyopathy: the European Anderson-Fabry Disease Survey

1 reference

12 December 2020

Role of cardiac MRI in evaluating patients with Anderson-Fabry disease: assessing cardiac effects of long-term enzyme replacement therapy.

1 reference

12 December 2020

Sex hormone receptor gene variation associated with phenotype in male hypertrophic cardiomyopathy patients

1 reference

12 December 2020

Review and metaanalysis of the frequency of familial dilated cardiomyopathy.

1 reference

12 December 2020

The influence of the angiotensin I converting enzyme genotype in familial hypertrophic cardiomyopathy varies with the disease gene mutation

1 reference

12 December 2020

Characteristics and clinical significance of late gadolinium enhancement by contrast-enhanced magnetic resonance imaging in patients with hypertrophic cardiomyopathy

1 reference

12 December 2020

Hypertrophic cardiomyopathy: histopathological features of sudden death in cardiac troponin T disease

1 reference

12 December 2020

Risk Factors for Malignant Ventricular Arrhythmias in Lamin A/C Mutation Carriers

1 reference

12 December 2020

Genome-wide mapping of modifier chromosomal loci for human hypertrophic cardiomyopathy

1 reference

12 December 2020

A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy

1 reference

12 December 2020

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

1 reference

12 December 2020

Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy

1 reference

12 December 2020

Targeted next-generation sequencing for the molecular genetic diagnostics of cardiomyopathies.

1 reference

12 December 2020

Genetic variation in the alternative splicing regulator RBM20 is associated with dilated cardiomyopathy.

1 reference

12 December 2020

Lamin A/C deficiency as a cause of familial dilated cardiomyopathy

1 reference

12 December 2020

Sustained alpha-sarcoglycan gene expression after gene transfer in limb-girdle muscular dystrophy, type 2D.

1 reference

12 December 2020

Nexilin mutations destabilize cardiac Z-disks and lead to dilated cardiomyopathy

1 reference

12 December 2020

Diagnostic, prognostic, and therapeutic implications of genetic testing for hypertrophic cardiomyopathy

1 reference

12 December 2020

Multiple mutations in genetic cardiovascular disease: a marker of disease severity?

1 reference

12 December 2020

Historical trends in reported survival rates in patients with hypertrophic cardiomyopathy

1 reference

12 December 2020

Next-generation sequencing entering the clinical arena

1 reference

12 December 2020

2011 ACCF/AHA Guideline for the Diagnosis and Treatment of Hypertrophic Cardiomyopathy: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines. Developed in collaboration with the Ameri

1 reference

12 December 2020

Mutations in NEXN, a Z-disc gene, are associated with hypertrophic cardiomyopathy

1 reference

12 December 2020

Clinical Features and Outcome of Hypertrophic Cardiomyopathy Associated With Triple Sarcomere Protein Gene Mutations

1 reference

12 December 2020

Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy

1 reference

12 December 2020

Treatment with selumetinib preserves cardiac function and improves survival in cardiomyopathy caused by mutation in the lamin A/C gene.

1 reference

12 December 2020

Use of cardiovascular magnetic resonance for risk stratification in chronic heart failure: prognostic value of late gadolinium enhancement in patients with non-ischaemic dilated cardiomyopathy

1 reference

12 December 2020

A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation

1 reference

12 December 2020

10.1007/S00108-011-2988-Z

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22388920%20AND%20SRC:MED&resulttype=core&format=json

24 January 2020

1 reference