Prevalence of HCM and long QT syndrome mutations in young sudden cardiac death-related cases. - sprookjes - yvandenbroek - TriplyDB

Prevalence of HCM and long QT syndrome mutations in young sudden cardiac death-related cases.

Prevalence of HCM and long QT syndrome mutations in young sudden cardiac death-related cases.

http://www.wikidata.org/entity/Q33159946

about

Genetic screening in sudden cardiac death in the young can save future lives Exercise restrictions trigger psychological difficulty in active and athletic adults with hypertrophic cardiomyopathy.Familial hypertrophic cardiomyopathy associated with a new mutation in gene MYBPC3.Genetics of hypertrophic cardiomyopathy: advances and pitfalls in molecular diagnosis and therapy.A comparison of genetic findings in sudden cardiac death victims and cardiac patients: the importance of phenotypic classification.Clinical interpretation of genetic variants in arrhythmogenic right ventricular cardiomyopathy.Detection of genetic variation in KCNQ1 gene by high-resolution melting analysis in a prospective-based series of postmortem negative sudden death: comparison of results obtained in fresh frozen and formalin-fixed paraffin-embedded tissues.Sequenom MassARRAY approach in the arrhythmogenic right ventricular cardiomyopathy post-mortem setting: clinical and forensic implications

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Prevalence of HCM and long QT syndrome mutations in young sudden cardiac death-related cases.

http://www.wikidata.org/entity/Q33159946

description

2011 nî lūn-bûn

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2011 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2011 թվականի ապրիլին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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Prevalence of HCM and long QT ...... n cardiac death-related cases.

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Prevalence of HCM and long QT ...... n cardiac death-related cases.

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Prevalence of HCM and long QT ...... n cardiac death-related cases.

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Prevalence of HCM and long QT ...... n cardiac death-related cases.

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Prevalence of HCM and long QT ...... n cardiac death-related cases.

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Prevalence of HCM and long QT ...... n cardiac death-related cases.

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International Journal of Legal Medicine

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Prevalence of HCM and long QT ...... n cardiac death-related cases.

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Alejandro Blanco-Verea

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Catarina Allegue

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Luis Concheiro

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Marisol Rodríguez-Calvo

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P2860

Single-gene mutations and increased left ventricular wall thickness in the community: the Framingham Heart Study

Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test

Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2

Coding sequence rare variants identified in MYBPC3, MYH6, TPM1, TNNC1, and TNNI3 from 312 patients with familial or idiopathic dilated cardiomyopathy

Sudden cardiac death with apparently normal heart.

Long QT syndrome in neonates: conduction disorders associated with HERG mutations and sinus bradycardia with KCNQ1 mutations.

Sudden arrhythmic death syndrome: familial evaluation identifies inheritable heart disease in the majority of families.

Risk stratification for sudden cardiac death in hypertrophic cardiomyopathy: systematic review of clinical risk markers.

A new approach to long QT syndrome mutation detection by Sequenom MassARRAY system.

Genomic structure of three long QT syndrome genes: KVLQT1, HERG, and KCNE1.

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4

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Angel Carracedo

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