DOCSLIB.ORG
Explore
Sign Up
Log In
Upload
Search
Home
» Tags
» Brugada Syndrome
Brugada Syndrome
Towards Mutation-Specific Precision Medicine in Atypical Clinical
Expanded Genetic Screening Panel for the Ashkenazi Jewish Population B
Brugada Syndrome
Brugada Syndrome: Clinical Care Amidst Pathophysiological Uncertainty
Recurrent Syncope in the Andersen Tawil Syndrome E Cardiac Or Neurological?
Test Requisition MOLECULAR DIAGNOSTICS LABORATORY
Relevance of Electrolytic Balance in Channelopathies
GENETIC TESTING REQUISITION Please Ship All
Update on the Diagnosis and Management of Familial Long QT Syndrome
Mitochondrial DNA Polymorphisms in Andersen–Tawil Syndrome
Brugada Syndrome Versus ARVC/D Dr
Diagnosis, Management and Therapeutic Strategies for Congenital
Brugada Syndrome Genetic Testing
Brugada Syndrome and Minors Forms of Arrhytmogenic Right Ventricular Cardiomyopathy/Dysplasia Phenotype Overlapping
Blueprint Genetics Cardiomyopathy Panel
Blueprint Genetics Comprehensive Cardiology Panel
Brugada Phenocopies
Brugada Syndrome
Top View
The Brugada Syndrome: a Rare Arrhythmia Disorder with Complex
Putative Role of Brugada Syndrome Genes in Familial Atrial Fibrillation
Functional Characterization of Two Novel Mutations in SCN5A Associated with Brugada Syndrome Identified in Italian Patients
Non-Neural Phenotype of Spinal and Bulbar Muscular Atrophy: Results
Structure of Human Nav1.5 Reveals the Fast Inactivation-Related Segments
Potassium Channels: Structures, Diseases, and Modulators
Guidelines on Clinical Presentation and Management of Non‐Dystrophic
Episodic Neurologic Disorders: Syndromes, Genes, and Mechanisms
Molecular and Genetic Basis of Sudden Cardiac Death
Role of Provocable Brugada ECG Pattern in the Correct Risk Stratification for Major Arrhythmic Events
The French National Protocol for Kennedy's Disease (SBMA)
Liddle Syndrome Precision Panel
Guidelines for the Diagnosis and Management of Brugada Syndrome
Brugada Syndrome
Sodium Channels
Disease-Targeted Sequencing of Ion Channel Genes Identifies De Novo
Brugada Syndrome: Oligogenic Or Mendelian Disease?
Expanded Genetic Screening Panel for the Ashkenazi Jewish Population
Diagnosed Cases of Rare Diseases at CENTOGENE January 2012 to June 2016
Genetics and Cardiac Channelopathies
Channelopathies That Lead to Sudden Cardiac Death: Clinical and Genetic Aspects
Download Download
Nav1.5 E1053K Mutation Causing Brugada Syndrome Blocks Binding to Ankyrin-G and Expression of Nav1.5 on the Surface of Cardiomyocytes Peter J
Centogene.Pdf
Brugada Syndrome
Channelopathies: a Link Between Brain and Heart: the Model of Epilepsy
Mexiletine-Responsive Erythromelalgia Due to a New Nav1.7 Mutation Showing Use-Dependent Current Fall-Off
Mechanisms of Arrhythmias in the Brugada Syndrome
Prevalence and Incidence of Rare Diseases: Bibliographic Data
A Case of Pediatric Brugada Syndrome Brynn E
Ion Channel Diseases
Pathophysiological Role of Omega Pore Current in Channelopathies
Arrhythmogenic Right Ventricular Dysplasia and Brugada Syndrome Overlap
Mendelian Disorders Among Jews
Hyperkalemic Periodic Paralysis: Case Report with a SCNA4 Gene Mutation and Literature Review
Long QT Syndrome (LQTS)