Juvenile sudden death in a family with polymorphic ventricular arrhythmias caused by a novel RyR2 gene mutation: evidence of specific morphological substrates-Reference-Cited by-同舟云学术

Juvenile sudden death in a family with polymorphic ventricular arrhythmias caused by a novel RyR2 gene mutation: evidence of specific morphological substrates

Published:2005-07 Issue:7 Volume:36 Page:761-767
ISSN:0046-8177
Container-title:Human Pathology
language:en
Short-container-title:Human Pathology

Author:

d'Amati Giulia,Bagattin Alessia,Bauce Barbara,Rampazzo Alessandra,Autore Camillo,Basso Cristina,King Kathy,Romeo Maria Daniela,Gallo Pietro,Thiene Gaetano,Danieli Gian Antonio,Nava Andrea

Publisher

Elsevier BV

Subject

Pathology and Forensic Medicine

Reference25 articles.

1. Postmortem diagnosis in sudden cardiac death victims: macroscopic, microscopic and molecular findings;Basso;Cardiovasc Res,2001

2. Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2);Tiso;Hum Mol Genet,2001

3. Screening for ryanodine receptor type 2 mutations in families with effort-induced polymorphic ventricular arrhythmias and sudden death: early diagnosis of asymptomatic carriers;Bauce;J Am Coll Cardiol,2002

4. Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia;Priori;Circulation,2001

5. Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia;Laitinen;Circulation,2001

Cited by 59 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. RYR2 receptor gene mutation associated with catecholaminergic polymorphic ventricular tachycardia in children: a case report & literature review;Translational Pediatrics;2024-02

2. Increased Ca ²⁺ Transient Underlies RyR2-Related Left Ventricular Noncompaction;Circulation Research;2023-07-07

3. RyR2 Serine-2030 PKA Site Governs Ca ²⁺ Release Termination and Ca ²⁺ Alternans;Circulation Research;2023-01-20

4. Correction: “Ryanopathies” and RyR2 dysfunctions: can we further decipher them using in vitro human disease models?;Cell Death & Disease;2022-11-30

5. A novel mutation in ryanodine receptor 2 (RYR2) genes at c.12670G>T associated with focal epilepsy in a 3-year-old child;Frontiers in Pediatrics;2022-10-19