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Publications by Richard D Bagnall
Exome Sequencing Identifies a Mutation in the ACTN2 Gene in a Family With Idiopathic Ventricular Fibrillation, Left Ventricular Noncompaction, and Sudden Death
BMC Medical Genetics
Genetics
Related publications
Left Ventricular Noncompaction
Sudden Cardiac Death in Isolated Right Ventricular Hypertrabeculation/Noncompaction Cardiomyopathy
Annals of Noninvasive Electrocardiology
Medicine
Cardiovascular Medicine
Physiology
Cardiology
Left Ventricular Noncompaction
Circulation Journal
Medicine
Cardiovascular Medicine
Cardiology
Whole-Exome Sequencing Identifies a Potential TTN Mutation in a Multiplex Family With Inguinal Hernia
Hernia : the journal of hernias and abdominal wall surgery
Surgery
Letter by Stollberger and Finsterer Regarding Article, "Mortality and Sudden Death in Pediatric Left Ventricular Noncompaction in a Tertiary Referral Center"
Circulation
Cardiovascular Medicine
Physiology
Cardiology
Single Nucleotide Polymorphisms in the Obscurin Gene and Left Ventricular Hypertrabeculation (Noncompaction)
Cardiology Research and Cardiovascular Medicine
Radiofrequency Energy Induced Ventricular Fibrillation in a Case of Idiopathic Premature Ventricular Contraction Originating From the Left Ventricular Papillary Muscle
Internal Medicine
Internal Medicine
Medicine
Whole Exome Sequencing Identifies a Novel and a Recurrent Mutation inBBS2Gene in a Family With Bardet-Biedl Syndrome
BioMed Research International
Immunology
Molecular Biology
Biochemistry
Microbiology
Medicine
Genetics
A Female Patient of Brugada Syndrome With an Episode of Ventricular Fibrillation and Family History of Sudden Death
Japanese Journal of Electrocardiology
