(Q37445574)

20 August 2017

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title

Prognostic factors in chronic heart failure. A review of serum biomarkers, metabolic changes, symptoms, and scoring systems (English)

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20 August 2017

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chronic heart failure

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2

Stefan D Anker

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20 August 2017

1

Mitja Lainscak

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20 August 2017

1 March 2009

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20 August 2017

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20 August 2017

34

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20 August 2017

2

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20 August 2017

141-147

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Genotype, phenotype: upstairs, downstairs in the family of cardiomyopathies

20 August 2017

1 reference

https://api.crossref.org/works/10.1007%2FS00059-009-3211-Z

Molecular mechanisms of inherited cardiomyopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-009-3211-Z

Echocardiographic measurements in normal subjects from infancy to old age.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-009-3211-Z

Right ventricular dysplasia: a report of 24 adult cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-009-3211-Z

Prevalence of hypertrophic cardiomyopathy in a general population of young adults. Echocardiographic analysis of 4111 subjects in the CARDIA Study. Coronary Artery Risk Development in (Young) Adults

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-009-3211-Z

Experience from clinical genetics in hypertrophic cardiomyopathy: proposal for new diagnostic criteria in adult members of affected families

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-009-3211-Z

Idiopathic restrictive cardiomyopathy is part of the clinical expression of cardiac troponin I mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-009-3211-Z

Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-009-3211-Z

Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the Definition and Classification of cardiomyopathies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-009-3211-Z

21 January 2018

1 reference

12 December 2020

Left ventricular involvement in arrhythmogenic right ventricular cardiomyopathy - a scintigraphic and echocardiographic study.

1 reference

12 December 2020

Idiopathic Dilated Cardiomyopathy

1 reference

12 December 2020

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

12 December 2020

Hypertrophic cardiomyopathy: the interrelation of disarray, fibrosis, and small vessel disease

1 reference

12 December 2020

C-terminal titin deletions cause a novel early-onset myopathy with fatal cardiomyopathy.

1 reference

12 December 2020

Desmoglein-2 mutations in arrhythmogenic right ventricular cardiomyopathy: a genotype-phenotype characterization of familial disease

1 reference

12 December 2020

Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy

1 reference

12 December 2020

Restrictive Cardiomyopathy

1 reference

12 December 2020

Cardiac features of a novel autosomal recessive dilated cardiomyopathic syndrome due to defective importation of mitochondrial protein

1 reference

12 December 2020

The muscular dystrophies

1 reference

12 December 2020

Classification of the cardiomyopathies: a position statement from the European Society Of Cardiology Working Group on Myocardial and Pericardial Diseases.

1 reference

12 December 2020

Arrhythmogenic right ventricular dysplasia. Study of a selected population

1 reference

12 December 2020

Myocyte transdifferentiation: a possible pathogenetic mechanism for arrhythmogenic right ventricular cardiomyopathy

1 reference

12 December 2020

Biventricular involvement in a Turkish boy with palmoplantar hyperkeratosis and curly hair, an unusual presentation of Naxos-Carvajal syndrome

1 reference

12 December 2020

Regulatory mutations in transforming growth factor-beta3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1

1 reference

12 December 2020

Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy

1 reference

12 December 2020

Myofilament protein gene mutation screening and outcome of patients with hypertrophic cardiomyopathy

1 reference

12 December 2020

A cathepsin D-cleaved 16 kDa form of prolactin mediates postpartum cardiomyopathy.

1 reference

12 December 2020

Underlying causes and long-term survival in patients with initially unexplained cardiomyopathy

1 reference

12 December 2020

Proposal for contemporary screening strategies in families with hypertrophic cardiomyopathy

1 reference

12 December 2020

Age- and Training-Dependent Development of Arrhythmogenic Right Ventricular Cardiomyopathy in Heterozygous Plakoglobin-Deficient Mice

1 reference

12 December 2020

Epidermolytic palmoplantar keratoderma with woolly hair and dilated cardiomyopathy

1 reference

12 December 2020

Shared genetic causes of cardiac hypertrophy in children and adults

1 reference

12 December 2020

Frequency and phenotypes of familial dilated cardiomyopathy.

1 reference

12 December 2020

Diagnosis of arrhythmogenic right ventricular dysplasia/cardiomyopathy. Task Force of the Working Group Myocardial and Pericardial Disease of the European Society of Cardiology and of the Scientific Council on Cardiomyopathies of the International S

1 reference

12 December 2020

Novel mutation in desmoplakin causes arrhythmogenic left ventricular cardiomyopathy

1 reference

12 December 2020

Neonatal, lethal noncompaction of the left ventricular myocardium is allelic with Barth syndrome

1 reference

12 December 2020

Cardiomyopathies: is it time for a molecular classification?

1 reference

12 December 2020

Autosomal dominant myofibrillar myopathy with arrhythmogenic right ventricular cardiomyopathy linked to chromosome 10q

1 reference

12 December 2020

Histological evidence of left ventricular involvement in arrhythmogenic right ventricular dysplasia

1 reference

12 December 2020

Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathy

1 reference

12 December 2020

Cardiac arrest and sudden death in competitive athletes with arrhythmogenic right ventricular dysplasia

1 reference

12 December 2020

Mutations in ZASP define a novel form of muscular dystrophy in humans

1 reference

12 December 2020

American College of Cardiology/European Society of Cardiology clinical expert consensus document on hypertrophic cardiomyopathy. A report of the American College of Cardiology Foundation Task Force on Clinical Expert Consensus Documents and the Euro

1 reference

12 December 2020

Prevalence and etiology of idiopathic dilated cardiomyopathy (summary of a National Heart, Lung, and Blood Institute workshop

1 reference

12 December 2020

Cardiac abnormalities in familial palmoplantar keratosis

1 reference

12 December 2020

Isolated left ventricular non-compaction: increasing recognition of this distinct, yet 'unclassified' cardiomyopathy

1 reference

12 December 2020

Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene

1 reference

12 December 2020

Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease).

1 reference

12 December 2020

Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma

1 reference

12 December 2020

Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia.

1 reference

12 December 2020

Hypertrophic cardiomyopathy: a systematic review

1 reference

12 December 2020

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

1 reference

12 December 2020

"Auricularization' of right ventricular pressure curve

1 reference

12 December 2020

Familial dilated cardiomyopathy: cardiac abnormalities are common in asymptomatic relatives and may represent early disease

1 reference

12 December 2020

Gene for arrhythmogenic right ventricular cardiomyopathy with diffuse nonepidermolytic palmoplantar keratoderma and woolly hair (Naxos disease) maps to 17q21

1 reference

12 December 2020

Cardiovascular causes of sudden death in young individuals including athletes

1 reference

12 December 2020

Comparison of modes of death and cardiac necropsy findings in fatal acute myocardial infarction in men and women >75 years of age

1 reference

12 December 2020

Arrhythmogenic right ventricular cardiomyopathy due to a novel plakophilin 2 mutation: wide spectrum of disease in mutation carriers within a family

1 reference

12 December 2020

Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathy

1 reference

12 December 2020

Requirement of plakophilin 2 for heart morphogenesis and cardiac junction formation

1 reference

12 December 2020

Recessive arrhythmogenic right ventricular dysplasia due to novel cryptic splice mutation in PKP2.

1 reference

12 December 2020

Genetically determined myocarditis: clinical presentation and immunological characteristics

1 reference

12 December 2020

Left ventricular involvement in arrhythmogenic right ventricular cardiomyopathy demonstrated by multidetector-row computed tomography.

1 reference

12 December 2020

Arrhythmogenic right ventricular cardiomyopathy with left ventricular involvement and aortic dissection

1 reference

12 December 2020

Isolated noncompaction of the myocardium

1 reference

12 December 2020

Genetic testing and genetic counseling in cardiovascular genetic medicine: overview and preliminary recommendations

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

Report of the WHO/ISFC task force on the definition and classification of cardiomyopathies

1 reference

12 December 2020

Hypertrophic cardiomyopathy and sudden death in the young: pathologic evidence of myocardial ischemia.

1 reference

12 December 2020

Clinical indications for genetic testing in familial sudden cardiac death syndromes: an HRUK position statement

1 reference

12 December 2020

Genetics of dilated cardiomyopathy

1 reference

12 December 2020

Evolution of left ventricular involvement in arrhythmogenic right ventricular cardiomyopathy

1 reference

12 December 2020

Long-term follow-up of 34 adults with isolated left ventricular noncompaction: a distinct cardiomyopathy with poor prognosis

1 reference

12 December 2020

Historical trends in reported survival rates in patients with hypertrophic cardiomyopathy

1 reference

12 December 2020

Homozygous mutation of desmocollin-2 in arrhythmogenic right ventricular cardiomyopathy with mild palmoplantar keratoderma and woolly hair.

1 reference

12 December 2020

Isolated ventricular non-compaction of the myocardium in adults

1 reference

12 December 2020

Prevalence, Clinical Significance, and Genetic Basis of Hypertrophic Cardiomyopathy With Restrictive Phenotype

1 reference

12 December 2020

Review on the genetics of arrhythmogenic right ventricular dysplasia.

1 reference

12 December 2020

Novel mutation in cardiac troponin I in recessive idiopathic dilated cardiomyopathy.

1 reference

12 December 2020

A novel dominant mutation in plakoglobin causes arrhythmogenic right ventricular cardiomyopathy

1 reference

12 December 2020

Mechanisms of disease: molecular genetics of arrhythmogenic right ventricular dysplasia/cardiomyopathy

1 reference

12 December 2020

Isolated noncompaction of ventricular myocardium associated with fatal ventricular fibrillation.

1 reference

12 December 2020

Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy

1 reference

12 December 2020

ARVC with left ventricular involvement in a young woman.

1 reference

12 December 2020

Clinical presentation and genetic analysis of a five generation Chinese family with isolated left ventricular noncompaction

1 reference

12 December 2020

[Right ventricular tachyarrhythmias--diagnostics and therapy]

1 reference

12 December 2020

Right ventricular cardiomyopathy and sudden death in young people

1 reference

12 December 2020

Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)

1 reference

12 December 2020

Naxos disease and Carvajal syndrome: cardiocutaneous disorders that highlight the pathogenesis and broaden the spectrum of arrhythmogenic right ventricular cardiomyopathy

1 reference

12 December 2020

Changes in myocardial cytoskeletal intermediate filaments and myocyte contractile dysfunction in dilated cardiomyopathy: an in vivo study in humans

1 reference

12 December 2020

Role of genetic analysis in the management of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy

1 reference

12 December 2020

Hypertrophic cardiomyopathy: the genetic determinants of clinical disease expression

1 reference

12 December 2020

A recessive mutation in desmoplakin causes arrhythmogenic right ventricular dysplasia, skin disorder, and woolly hair

1 reference

12 December 2020

Isolated noncompaction of the myocardium in adults

1 reference

12 December 2020

Familial dilated cardiomyopathy

1 reference

12 December 2020

Arrhythmogenic right ventricular cardiomyopathy with an initial manifestation of severe left ventricular impairment and normal contraction of the right ventricle

1 reference

12 December 2020

Isolated noncompaction of the ventricular myocardium in a patient presenting with subarachnoid hemorrhage

1 reference

12 December 2020

Clinical expression of plakophilin-2 mutations in familial arrhythmogenic right ventricular cardiomyopathy

1 reference

12 December 2020

10.1007/S00059-009-3211-Z

Identifiers

DOI

1 reference

20 August 2017

1 reference

PubMed ID

19370331