Genotype-phenotype relationship in patients with arrhythmogenic right ventricular cardiomyopathy caused by desmosomal gene mutations: A systematic review and meta-analysis. (Q37605121)

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scientific article published on 25 January 2017

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English	Genotype-phenotype relationship in patients with arrhythmogenic right ventricular cardiomyopathy caused by desmosomal gene mutations: A systematic review and meta-analysis.	scientific article published on 25 January 2017

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scholarly article

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9 April 2020

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6 November 2020

Genotype-phenotype relationship in patients with arrhythmogenic right ventricular cardiomyopathy caused by desmosomal gene mutations: A systematic review and meta-analysis (English)

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9 April 2020

arrhythmogenic right ventricular cardiomyopathy

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19 September 2019

6 November 2020

genetic variation

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14 September 2019

biomedical investigative technique

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19 September 2019

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6 November 2020

systematic review

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based on heuristic

inferred from title

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based on heuristic

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2

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Zhenyan Xu

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Cen Wang

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9 April 2020

Lin Huang

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Qiongqiong Zhou

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Jinzhu Hu

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9 April 2020

Xiaoshu Cheng

7

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Kui Hong

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25 January 2017

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6 November 2020

Scientific Reports

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6 November 2020

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9 April 2020

41387

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9 April 2020

copyright license

Creative Commons Attribution 4.0 International

7 references

Europe PubMed Central

22 March 2019

Europe PubMed Central

20 June 2019

Europe PubMed Central

30 June 2019

Europe PubMed Central

17 June 2019

Europe PubMed Central

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Europe PubMed Central

19 September 2019

Europe PubMed Central

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copyright status

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on focus list of Wikimedia project

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https://scigraph.springernature.com/pub.10.1038/srep41387

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High Arrhythmic Burden but Low Mortality during Long-term Follow-up in Arrhythmogenic Right Ventricular Cardiomyopathy

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23 August 2017

Arrhythmogenic right ventricular cardiomyopathy, clinical manifestations, and diagnosis

1 reference

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23 August 2017

Phenotypic expression is a prerequisite for malignant arrhythmic events and sudden cardiac death in arrhythmogenic right ventricular cardiomyopathy.

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23 August 2017

Titin and desmosomal genes in the natural history of arrhythmogenic right ventricular cardiomyopathy

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23 August 2017

Stop-gain mutations in PKP2 are associated with a later age of onset of arrhythmogenic right ventricular cardiomyopathy

1 reference

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23 August 2017

Compound and digenic heterozygosity predicts lifetime arrhythmic outcome and sudden cardiac death in desmosomal gene-related arrhythmogenic right ventricular cardiomyopathy

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23 August 2017

Desmin mutations and arrhythmogenic right ventricular cardiomyopathy

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23 August 2017

Phospholamban R14del mutation in patients diagnosed with dilated cardiomyopathy or arrhythmogenic right ventricular cardiomyopathy: evidence supporting the concept of arrhythmogenic cardiomyopathy

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23 August 2017

Clinical phenotype and diagnosis of arrhythmogenic right ventricular cardiomyopathy in pediatric patients carrying desmosomal gene mutations.

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23 August 2017

Arrhythmogenic right ventricular dysplasia/cardiomyopathy: pathogenic desmosome mutations in index-patients predict outcome of family screening: Dutch arrhythmogenic right ventricular dysplasia/cardiomyopathy genotype-phenotype follow-up study

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23 August 2017

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

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23 August 2017

De novo desmin-mutation N116S is associated with arrhythmogenic right ventricular cardiomyopathy

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23 August 2017

Desmosomal gene analysis in arrhythmogenic right ventricular dysplasia/cardiomyopathy: spectrum of mutations and clinical impact in practice

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23 August 2017

Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the Task Force Criteria

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23 August 2017

Comprehensive desmosome mutation analysis in north americans with arrhythmogenic right ventricular dysplasia/cardiomyopathy

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5264593

23 August 2017

Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement

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23 August 2017

Genetic evaluation of cardiomyopathy--a Heart Failure Society of America practice guideline

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23 August 2017

Clinical and genetic characterization of families with arrhythmogenic right ventricular dysplasia/cardiomyopathy provides novel insights into patterns of disease expression

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23 August 2017

Trends in sudden cardiovascular death in young competitive athletes after implementation of a preparticipation screening program

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23 August 2017

Ultrastructural evidence of intercalated disc remodelling in arrhythmogenic right ventricular cardiomyopathy: an electron microscopy investigation on endomyocardial biopsies

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23 August 2017

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

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23 August 2017

Clinical features of arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in plakophilin-2

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23 August 2017

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

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23 August 2017

Cardiac MR findings and potential diagnostic pitfalls in patients evaluated for arrhythmogenic right ventricular cardiomyopathy

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6 September 2017

Genetics of arrhythmogenic right ventricular cardiomyopathy: a practical guide for physicians

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HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA).

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Approach to family screening in arrhythmogenic right ventricular dysplasia/cardiomyopathy.

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Clinical Presentation, Long-Term Follow-Up, and Outcomes of 1001 Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Patients and Family Members

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LMNA cardiomyopathy detected in Japanese arrhythmogenic right ventricular cardiomyopathy cohort.

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Age-dependent clinical and genetic characteristics in Japanese patients with arrhythmogenic right ventricular cardiomyopathy/dysplasia

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Genome-wide association identifies a deletion in the 3' untranslated region of striatin in a canine model of arrhythmogenic right ventricular cardiomyopathy

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Arrhythmogenic right ventricular cardiomyopathy: implications of next-generation sequencing in appropriate diagnosis.

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Relationships Between Clinical Characteristics and Decreased Plakoglobin and Connexin 43 Expressions in Myocardial Biopsies From Patients With Arrhythmogenic Right Ventricular Cardiomyopathy.

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Function of a novel plakophilin-2 mutation in the abnormal expression of connexin43 in a patient with arrhythmogenic right ventricular cardiomyopathy

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Electrocardiographic predictors of electroanatomic scar size in arrhythmogenic right ventricular cardiomyopathy: implications for arrhythmic risk stratification

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Comparison of clinical features of arrhythmogenic right ventricular cardiomyopathy in men versus women.

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1 September 2018

Prevalence and significance of rare RYR2 variants in arrhythmogenic right ventricular cardiomyopathy/dysplasia: Results of a systematic screening

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Impact of genotype on clinical course in arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated mutation carriers

1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Desmoglein-2 and desmocollin-2 mutations in dutch arrhythmogenic right ventricular dysplasia/cardiomypathy patients: results from a multicenter study

1 reference

https://pubmed.ncbi.nlm.nih.gov/28120905

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prolonged Electromechanical Interval Unmasks Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy in the Subclinical Stage

1 reference

https://pubmed.ncbi.nlm.nih.gov/28120905

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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10.1038/SREP41387

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9 April 2020

1 reference

Europe PubMed Central

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9 April 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28120905%20AND%20SRC:MED&resulttype=core&format=json

9 April 2020

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