Clinical Spectrum of PRKAG2 Syndrome-Reference-Cited by-同舟云学术

Clinical Spectrum of PRKAG2 Syndrome

Published:2016-01 Issue:1 Volume:9 Page:
ISSN:1941-3149
Container-title:Circulation: Arrhythmia and Electrophysiology
language:en
Short-container-title:Circ: Arrhythmia and Electrophysiology

Author:

Porto Andrea Giuseppe¹,Brun Francesca¹,Severini Giovanni Maria¹,Losurdo Pasquale¹,Fabris Enrico¹,Taylor Matthew R.G.¹,Mestroni Luisa¹,Sinagra Gianfranco¹

Affiliation:

1. From the Cardiovascular Department “Ospedali Riuniti and University of Trieste,” Trieste, Italy (A.G.P., F.B., P.L., E.F., G.S.); Molecular Medicine Department, Institute for Maternal and Child Health, IRCCS Burlo Garofolo, Trieste, Italy (G.M.S.); and Cardiovascular Institute and Adult Medical Genetics, Department of Medicine, University of Colorado Denver, Aurora (M.R.G.T., L.M.).

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Link

https://www.ahajournals.org/doi/pdf/10.1161/CIRCEP.115.003121

Reference45 articles.

1. Anatomic Findings in a Case of Ventricular Pre-Excitation (WPW) Terminating in Complete Atrioventricular Block

2. Familial occurrence of sinus bradycardia, short PR interval, intraventricular conduction defects, recurrent supraventricular tachycardia, and cardiomegaly

3. Syncope in hypertrophic cardiomyopathy. II. Coexistence of atrioventricular block and Wolff-Parkinson-White syndrome

4. Familial Hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3.

5. Identification of a Gene Responsible for Familial Wolff–Parkinson–White Syndrome

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2. When Paying Attention Pays Back: Missense Mutation c.1006G>A p. (Val336Ile) in PRKAG2 Gene Causing Left Ventricular Hypertrophy and Conduction Abnormalities in a Caucasian Patient: Case Report and Literature Review;International Journal of Molecular Sciences;2024-08-23

3. Echocardiographic Findings in Children of Patients Diagnosed with PRKAG2 Syndrome;Arquivos Brasileiros de Cardiologia;2024-08

4. Achados Ecocardiográficos em Crianças de Pacientes com Diagnóstico de Síndrome do PRKAG2;Arquivos Brasileiros de Cardiologia;2024-08

5. PRKAG2 Variant, Motor Neuron Disease, and Parkinsonism: Fortuitous Association or a Potentially Underestimated Pathophysiological Mechanism?;Muscles;2024-07-25