• 'Behr syndrome' with OPA1 compound heterozygote mutations
• <em>SCN5A</em> Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in <em>SCN5A</em> Families
• 2020 APHRS/HRS expert consensus statement on the investigation of decedents with sudden unexplained death and patients with sudden cardiac arrest, and of their families
• 2020 APHRS/HRS expert consensus statement on the investigation of decedents with sudden unexplained death and patients with sudden cardiac arrest, and of their families
• A randomized controlled trial of liposomal cyclosporine A for inhalation in the prevention of bronchiolitis obliterans syndrome following lung transplantation
• Accuracy of Placement of Pedicle Screws in the Lumbosacral Region of Dogs Using 3D-Printed Patient-Specific Drill Guides
• An OPA3 gene mutation is responsible for the disease associating optic atrophy and cataract with extrapyramidal signs
• Andersen-Tawil syndrome: deep phenotyping reveals significant cardiac and neuromuscular morbidity
• Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
• BCG vaccination provides protection against IAV but not SARS-CoV-2
• Behr syndrome
• Behr syndrome and hypergonadotropic hypogonadism
• Behr syndrome and hypertrophic cardiomyopathy in a family with a novel UCHL1 deletion
• Behr syndrome variant with tremor treated by VIM stimulation
• Behr syndrome with homozygous C19ORF12 mutation
• Behr syndrome: a clinicopathologic report
• Behr's disease or complicated heredofamilial infantile optic atrophy
• Biallelic Optic Atrophy 1 (<em>OPA1</em>) Related Disorder-Case Report and Literature Review
• Biventricular Myocardial Fibrosis and Sudden Death in Patients With Brugada Syndrome
• Brugada Syndrome
• Brugada syndrome and arrhythmogenic cardiomyopathy: overlapping disorders of the connexome?
• Brugada syndrome and reduced right ventricular outflow tract conduction reserve: a final common pathway?
• Cardiogenetics: the role of genetic testing for inherited arrhythmia syndromes and sudden death
• Catecholaminergic Polymorphic Ventricular Tachycardia
• Characteristics of Patients with Spontaneous Versus Drug-Induced Brugada Electrocardiogram: Sub-Analysis From the SABRUS
• Clinical Course of Three Postoperative Symptomatic COVID-19 Cases in Patients After Lung Lobectomy
• Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry
• COMPLICATED INFANTILE SIMPLE OPTIC ATROPHY OF BEHR. (BEHR'S SYNDROME)
• Concurrent OPA1 mutation and chromosome 3q deletion leading to Behr syndrome: a case report
• Confirmation of Cause of Death Via Comprehensive Autopsy and Whole Exome Molecular Sequencing in People With Epilepsy and Sudden Unexpected Death
• Coronary Artery Dissection and Myocardial Infarction With Nonobstructed Coronary Arteries: Insights From a UK Nationwide Autopsy-Based Registry-Brief Report
• Detection of acute ventilatory problems via magnetic induction in a newborn animal model
• Detection of viral antibodies in camel sera using magnetic particle spectroscopy
• Diagnosis, family screening, and treatment of inherited arrhythmogenic diseases in Europe: results of the European Heart Rhythm Association Survey
• Disconnected Pancreatic Duct Syndrome: Pancreatitis of the Disconnected Pancreas and Its Role in the Development of Diabetes Mellitus
• Dynamics of SARS-CoV-2 shedding in the respiratory tract depends on the severity of disease in COVID-19 patients
• Dynamics of urinary and respiratory shedding of Severe acute respiratory syndrome virus 2 (SARS-CoV-2) RNA excludes urine as a relevant source of viral transmission
• Early-onset Behr syndrome due to compound heterozygous mutations in OPA1
• Effectiveness of germicidal ultraviolet light to inactivate coronaviruses on personal protective equipment to reduce nosocomial transmission
• Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls
• ESC guidance for the diagnosis and management of cardiovascular disease during the COVID-19 pandemic: part 2-care pathways, treatment, and follow-up
• ESC guidance for the diagnosis and management of cardiovascular disease during the COVID-19 pandemic: part 2-care pathways, treatment, and follow-up
• European Society of Cardiology guidance for the diagnosis and management of cardiovascular disease during the COVID-19 pandemic: part 1-epidemiology, pathophysiology, and diagnosis
• European Society of Cardiology guidance for the diagnosis and management of cardiovascular disease during the COVID-19 pandemic: part 1-epidemiology, pathophysiology, and diagnosis
• Familial Behr syndrome-like phenotype with autosomal dominant inheritance
• Familial Evaluation in Idiopathic Ventricular Fibrillation: Diagnostic Yield and Significance of J Wave Syndromes
• Family History of Sudden Cardiac Death in the Young and Inherited Arrhythmia Syndromes: Awareness and Attitudes of General Practitioners and Private Practice Cardiologists
• Generation of optic atrophy 1 patient-derived induced pluripotent stem cells (iPS-OPA1-BEHR) for disease modeling of complex optic atrophy syndromes (Behr syndrome)
• Genetics and genomics of arrhythmic risk: current and future strategies to prevent sudden cardiac death
• Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
• Genotype-Phenotype Correlation of <em>SCN5A</em> Genotype in Patients With Brugada Syndrome and Arrhythmic Events: Insights From the SABRUS in 392 Probands
• Hereditary infantile optic atrophy with dominant transmission
• Heterozygous OPA1 mutations in Behr syndrome
• Impact of Lung Function Decline on Mortality in Lung Transplant Recipients: Long-Term Results From the L-CsA-i Study for the Prevention of Bronchiolitis Obliterans Syndrome
• Impact of the COVID-19 pandemic on the behaviour and health status of patients with COPD: results from the German COPD cohort COSYCONET
• Implantable loop recorders in Brugada syndrome
• Importance of Dedicated Units for the Management of Patients With Inherited Arrhythmia Syndromes
• Infantile optic atrophy with dominant mode of inheritance: a clinical and genetic study of 19 Danish families
• Interpretation and actionability of genetic variants in cardiomyopathies: a position statement from the European Society of Cardiology Council on cardiovascular genomics
• Investigation on Sudden Unexpected Death in the Young (SUDY) in Europe: results of the European Heart Rhythm Association Survey
• J-Wave Syndromes, SCN5A, and Cardiac Conduction Reserve: Two Sides of the Same Coin?
• J-Wave Syndromes: Where's the Scar?
• Leigh-like neuroimaging features associated with new biallelic mutations in OPA1
• Lessons From Bacille Calmette-Guérin for SARS-CoV-2 Vaccine Candidates
• Long-Term Outcomes of Brugada Substrate Ablation: A Report from BRAVO (Brugada Ablation of VF Substrate Ongoing Multicenter Registry)
• Longitudinal lung function measurements in single lung transplant recipients with chronic lung allograft dysfunction
• Lung Transplantation for Patients With COVID-19
• Management of Congenital Long-QT Syndrome: Commentary From the Experts
• Mechanism of the effects of sodium channel blockade on the arrhythmogenic substrate of Brugada syndrome
• Metabolic stroke in a patient with bi-allelic OPA1 mutations
• Molecular diagnosis and novel genes and phenotypes in a pediatric thoracic insufficiency cohort
• MRI abnormalities in Behr syndrome
• Musculoskeletal deformities in Behr syndrome
• Non-invasive detection of exercise-induced cardiac conduction abnormalities in sudden cardiac death survivors in the inherited cardiac conditions
• Not a pneumothorax again! Birt-Hogg-Dubé syndrome: a case report
• On a heredo-familial disease combining cataract, optic atrophy, extrapyramidal symptoms and certain defects of Friedreich's disease. (Its nosological position in relation to the Behr's syndrome, the Marinesco-Sjogren syndrome and Friedreich&#039
• Optic atrophy, Behr syndrome
• PERIMETRIC AND CAMPIMETRIC FINDINGS IN CASES OF BENIGN INFANTILE HEREDO-FAMILIAL OPTIC ATROPHY
• Posttraumatic Lymphedema after Open Fractures of the Lower Extremity-A Retrospective Cohort Analysis
• Potential Role of MRI Imaging for Myofascial Pain: A Scoping Review for the Clinicians and Theoretical Considerations
• Prevalence and Characteristics of Sleep Apnea in Intensive Care Unit Survivors After SARS-CoV-2 Pneumonia
• Psychosis in German prisoners: Comparison of the clinical appearance of psychotic disorder of an imprisoned population with a not detained community group
• Pulmonary embolism among critically ill patients with ARDS due to COVID-19
• Quantitative response of healthy muscle following the induction of capsaicin: an exploratory randomized controlled trial
• Rare Variation in Drug Metabolism and Long QT Genes and the Genetic Susceptibility to Acquired Long QT Syndrome
• Recessive optic atrophy, sensorimotor neuropathy and cataract associated with novel compound heterozygous mutations in OPA1
• Recurrent super-refractory status epilepticus and stroke like episode in a patient with Behr syndrome secondary to biallelic variants in OPA1 gene
• Reply: 'Behr syndrome' with OPA1 compound heterozygote mutations
• Reply: Early-onset Behr syndrome due to compound heterozygous mutations in OPA1
• Result of one-year, prospective follow-up of intensive care unit survivors after SARS-CoV-2 pneumonia
• Risk of Sudden Infant Death Syndrome Among Siblings of Children Who Died of Sudden Infant Death Syndrome in Denmark
• Role of subcutaneous implantable loop recorder for the diagnosis of arrhythmias in Brugada syndrome: A United Kingdom single-center experience
• Sex-Related Differences in Cardiac Channelopathies: Implications for Clinical Practice
• Single-cell RNA sequencing reveals ex vivo signatures of SARS-CoV-2-reactive T cells through 'reverse phenotyping'
• Subepicardial Cardiomyopathy: A Disease Underlying J-Wave Syndromes and Idiopathic Ventricular Fibrillation
• Sudden Cardiac Death Among Adolescents in the United Kingdom
• The genomic architecture of the Brugada syndrome
• The Utility of Sodium Channel Provocation in Unexplained Cardiac Arrest Survivors and Electrocardiographic Predictors of Ventricular Fibrillation Recurrence
• Transcriptional Dysregulation Underlies Both Monogenic Arrhythmia Syndrome and Common Modifiers of Cardiac Repolarization
• Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome