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Mashup Score: 3Genetic testing in children with Brugada syndrome: results from a large prospective registry - 1 year(s) ago
AbstractAims. A pathogenic/likely pathogenic (P/LP) variant in SCN5A is found in 20–25% of patients with Brugada syndrome (BrS). However, the diagnostic yield a
Source: OUP AcademicCategories: Cardiologists, Latest HeadlinesTweet-
Genetic testing in children with Brugada syndrome: diagnostic yield and prognostic significance 👉 https://t.co/PMRH6OuTwg @EuropaceEiC @GiulioConte9 @Dominik_Linz @FraSantoroMD @AndyZhangMD @marcovitoloMD @deasnostos @escardio #Brugadasyndrome #genetics #europace https://t.co/7qp1DDmoaF
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Mashup Score: 0Transcriptional Dysregulation Underlies Both Monogenic Arrhythmia Syndrome and Common Modifiers of Cardiac Repolarization - 1 year(s) ago
BACKGROUND: Brugada syndrome (BrS) is an inherited arrhythmia syndrome caused by loss-of-function variants in the cardiac sodium channel gene SCN5A (sodium voltage-gated channel alpha subunit 5) in ≈
Source: CirculationCategories: Cardiologists, Latest HeadlinesTweet-
Interesting study just out @CircAHA regarding #BrugadaSyndrome and role of #TBX5 Transcriptional Dysregulation Underlies Both Monogenic Arrhythmia Syndrome and Common Modifiers of Cardiac Repolarization. Thoughts @benoitbruneau @PorrelloER @DaveElliott_1 https://t.co/pWGOTJi8SY https://t.co/B35ahWgDBw
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Mashup Score: 3
The Illinois Democrat said his oldest daughter, Gwen Casten, went to bed Sunday night and never woke up in a heartbreaking statement Wednesday.
Source: New York PostCategories: Cardiologists, Latest HeadlinesTweet-
RIP & condolences. Most common cause of nocturnal #SuddenCardiacDeath is #BrugadaSyndrome. @UM_Cardiology Inherited Heart Disease program can screen for this in some cases. @vinniesee @wang_libin @UMmedschool @ummc https://t.co/835xYLDmRZ
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Mashup Score: 2Gene Therapy Rescues Mice With Cardiac Disorder - 2 year(s) ago
Scientists rescued mice with mutations identified in Brugada Syndrome patients from disease symptoms using gene therapy.
Categories: Future of Medicine, Latest HeadlinesTweet-
#GeneTherapy Rescues Mice With #CardiacDisorder Scientists rescued mice with mutations identified in #BrugadaSyndrome patients from disease symptoms using gene therapy. Learn more: https://t.co/xvX96Md0bA https://t.co/yTVfYKANlG
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Mashup Score: 0Gene Therapy Rescues Mice With Cardiac Disorder - 2 year(s) ago
Scientists rescued mice with mutations identified in Brugada Syndrome patients from disease symptoms using gene therapy.
Categories: Future of Medicine, Latest HeadlinesTweet-
#GeneTherapy Rescues Mice With #CardiacDisorder Scientists rescued mice with mutations identified in #BrugadaSyndrome patients from disease symptoms using gene therapy. Learn more: https://t.co/xvX96Md0bA https://t.co/harQdcJRaU
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Mashup Score: 9Association Between Deleterious SCN5A Variants and Ventricular Septal Defect in Young Patients With Brugada Syndrome: - 2 year(s) ago
Abstract Objectives This study aimed to investigate the clinical characteristics of young patients with Brugada syndrome (BrS) with ventricular septal defect (VSD) and explore their genetic backgro…
Source: JACC: Clinical ElectrophysiologyCategories: Expert Picks, Latest HeadlinesTweet-
In #BrugadaSyndrome (BrS) patients with #VSD, researchers find that altered blood flow in the #RVOT leads to fibrosis & electrophysiological changes, predisposing these patients to earlier clinical presentation of #BrS. https://t.co/Kd4Y5KtMIz #JACCCEP #EPeeps #CardioTwitter https://t.co/5Izlg2a2Wf
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Mashup Score: 14Brugada Syndrome: - 2 year(s) ago
Abstract Brugada syndrome (BrS) is an “inherited” condition characterized by predisposition to syncope and cardiac arrest, predominantly during sleep. The prevalence is ∼1:2,000, and is more common…
Source: JACC: Clinical ElectrophysiologyCategories: Expert Picks, Latest HeadlinesTweet-
Bookmark this state-of-the-art review in the new issue of #JACCCEP! Contemporary, comprehensive review of #BrugadaSyndrome by Dr. @AndrewKrahnMD and team: pathophysiology & practical recommendations for diagnosis, risk assessment, & management. https://t.co/oMqnrFYnVw #EPeeps https://t.co/wjMnmvhRq2
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Mashup Score: 0
The aim of this study was to provide the spectrum and prevalence of mutations in the 12 Brugada syndrome (BrS)–susceptibility genes discovered to date…
Source: www.sciencedirect.comCategories: Cardiologists, Latest HeadlinesTweet-
I would say that this paper is a nice confirmation of our work on #BrugadaSyndrome #genetics published in @JACCJournals in 2012 first name @CrottiLia 👇 https://t.co/1N6SHxlMV6 in collaboration with @MayoClinicWSRGH @MJAckermanMDPhD @JohnGiudicessi et coll... How young I was!🙂 https://t.co/L79oGLfWgL
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Mashup Score: 29Biventricular Myocardial Fibrosis and Sudden Death in Patients With Brugada Syndrome: - 3 year(s) ago
Abstract Background Electrophysiological, imaging, and pathological studies have reported the presence of subtle structural abnormalities in hearts from patients with Brugada syndrome (BrS). Howeve…
Categories: Expert Picks, Latest HeadlinesTweet-
New autopsy study suggests Brugada syndrome results in collagen deposition in the RV and LV myocardium: https://t.co/VPhy9KTSfm #JACC #CMR #BrugadaSyndrome #CardioTwitter #MedTwitter @TheACMG @DrCJMiles https://t.co/d8aCgwgw4s
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Mashup Score: 1Two zebras and a cardiac arrest: a case report of concomitant Brugada syndrome and an anomalous coronary artery - 3 year(s) ago
AbstractBackground. Discovering concomitant diagnoses results in a challenge to determine the true cause of a patient’s presentation. Evaluating this fully is v
Source: OUP AcademicCategories: Cardiology News and Journals, Latest HeadlinesTweet-
7/19 Upon discovery of coronary anomalies, care should still be taken to evaluate thoroughly and not label it as the only cause for #SuddenCardiacArrest #BrugadaSyndrome was found to be the culprit in this pt w/ concurrent anomalous RCA https://t.co/vOMrhGHlhm #EHJCaseReports https://t.co/1c77ChaK0Z
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RT @ESC_Journals: Genetic testing in children with Brugada syndrome: diagnostic yield and prognostic significance 👉 https://t.co/PMRH6OuTwg…