Myocardial perfusion defects in genotype-positive hypertrophic cardiomyopathy without left ventricular hypertrophy

RK Hughes , C Camaioni , KD Knott , E Quinn
EUROPEAN HEART JOURNAL-CARDIOVASCULAR IMAGING 20 195 -196

2019
267 Myocardial perfusion defects in genotype-positive hypertrophic cardiomyopathy without left ventricular hypertrophy

RK Hughes , C Camaioni , KD Knott , E Quinn
European Heart Journal-Cardiovascular Imaging 20 ( Supplement_2) jez101 -jez101

2019
325 Arrhythmogenic left ventricular cardiomyopathy and dilated cardiomyopathy: genotype-phenotype correlations

JA Bicho Augusto , R Eiros , E Nakou , S Moura-Ferreira
European Heart Journal-Cardiovascular Imaging 20 ( Supplement_2) jez102. 005 -jez102. 005

2019
RENDIMIENTO DIAGNÓSTICO DE LA AUTOPSIA MOLECULAR EN PACIENTES CON MUERTE SÚBITA CARDIACA Y CORAZÓN ESTRUCTURALMENTE NORMAL.

D Domingo , L Nunn , P Molina , P Syrris
PUBLICACIÓN OFICIAL DE LA SOCIEDAD VALENCIANA DE CARDIOLOGÍA 57 -57

1989
Influence of sex on cardiovascular outcomes in RBM20 variant carriers

D Cannie , A Protonotarios , P Syrris , A Sengupta
European Heart Journal 43 ( Supplement_2) ehac544. 1744 -ehac544. 1744

2022
Arrhythmic risk assessment in family members with arrhythmogenic cardiomyopathy associated desmosomal mutations

A Protonotarios , A Anastasakis , C Ritsatos , V Vlagouli
EUROPEAN HEART JOURNAL 36 272 -272

2015
X-linked Emery-Dreifuss muscular dystrophy is associated with a high risk of malignant ventricular arrhythmia

D Cannie , P Syrris , JF Rodriguez-Palomares , C Marini-Bettolo
European Heart Journal 44 ( Supplement_2) ehad655. 617 -ehad655. 617

2023
Cardiac abnormalities in patients with Leber's hereditary optic neuropathy

P Sorajja , MG Sweeney , R Chalmers , B Sachdev
Heart 89 ( 7) 791 -792

23
2003
Genetic regulation of myocardial fibrosis in hypertrophic cardiomyopathy

V Patel , P Syrris , C Coats , J Lucena
European Heart Journal 42 ( Supplement_1) ehab724. 1778 -ehab724. 1778

2
2021
Relation between non-sustained ventricular tachycardia and major arrhythmic events in patients with dilated cardiomyopathy caused by titin truncating variants

K Hirose , D Cannie , P Syrris , A Bakalakos
European Heart Journal 44 ( Supplement_2) ehad655. 1868 -ehad655. 1868

2023
2012
Long-term outcomes in hypertrophic cardiomyopathy caused by mutations in the cardiac troponin T gene

F Pasquale , P Syrris , G Quarta , CO Mahony
OXFORD UNIV PRESS 31 161 -162

2010
Idiopathic restrictive cardiomyopathy in children is caused by mutations in cardiac sarcomere protein genes

JP Kaski , P Syrris , M Burch , MTT Esteban
EUROPEAN HEART JOURNAL 28 102 -103

2007
A novel mutation in the endothelin B receptor gene in a patient with Shah-Waardenburg syndrome and Down syndrome

JP Boardman , P Syrris , SE Holder , NJ Robertson
Journal of Medical Genetics 38 ( 9) 646 -647

18
2001