1,382 results on '"Wilde, Arthur A M"'
Search Results
152. Brugada syndrome: in search of a genotype-phenotype relationship
153. Catecholaminergic Polymorphic Ventricular Tachycardia
154. Idiopathic Ventricular Fibrillation
155. The Outpatient Clinic for Cardiogenetics
156. Diagnosis, management and therapeutic strategies for congenital long QT syndrome.
157. Investigation on Sudden Unexpected Death in the Young (SUDY) in Europe: results of the European Heart Rhythm Association Survey.
158. Comparing clinical performance of current implantable cardioverter-defibrillator implantation recommendations in arrhythmogenic right ventricular cardiomyopathy.
159. Pregnancy in women with Brugada syndrome: Is there an increased arrhythmia risk? A case‐series report.
160. Genomic organisation and chromosomal localisation of two members of the KCND ion channel family, KCND2 and KCND3
161. A calcium sensor in the sodium channel modulates cardiac excitability
162. Variants in the 3′ untranslated region of the KCNQ1-encoded Kv7.1 potassium channel modify disease severity in patients with type 1 long QT syndrome in an allele-specific manner
163. A sodium-channel mutation causes isolated cardiac conduction disease
164. The site of origin of torsade de pointes
165. Facilitatory and inhibitory effects of SCN5A mutations on atrial fibrillation in Brugada syndrome
166. The patient with hypertrophic cardiomyopathy has a family
167. A highly specific biomarker for Brugada syndrome. Also too good to be true?
168. Continued misuse of orphan drug legislation: a life-threatening risk for mexiletine
169. Epidemiology of inherited arrhythmias
170. Symptoms and signs of syncope: a review of the link between physiology and clinical clues
171. Mutations in Conserved Amino Acids in the KCNQ1 Channel and Risk of Cardiac Events in Type-1 Long-QT Syndrome
172. Evolution of cardiac abnormalities in Becker muscular dystrophy over a 13-year period
173. The long QT syndrome: a novel missense mutation in the S6 region of the KVLQT1 gene
174. A new prediction model for ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy
175. Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events A GENIUS-CHD Study of Individual Participant Data
176. SCN5A variants in Brugada syndrome: True, true false, or false true
177. A Novel Early Onset Lethal Form of Catecholaminergic Polymorphic Ventricular Tachycardia Maps to Chromosome 7p14-p22
178. Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system?
179. In-hospital cardiac arrest is associated with use of non-antiarrhythmic QTc-prolonging drugs
180. Role of ATP-sensitive K+ channel current in ischemic arrhythmias
181. GENETICS OF CARDIAC ARRHYTHMIAS
182. Human RyR2 (Ryanodine Receptor 2) Loss-of-Function Mutations: Clinical Phenotypes and In Vitro Characterization.
183. Life-threatening arrhythmias with autosomal recessive TECRL variants.
184. Two siblings with early repolarization syndrome: clinical and genetic characterization by whole-exome sequencing.
185. Dutch Outcome in Implantable Cardioverter-Defibrillator Therapy: Implantable Cardioverter-Defibrillator-Related Complications in a Contemporary Primary Prevention Cohort.
186. Potassium Channel Activation and Arrhythmogenicity
187. Determination and Interpretation of the QT Interval
188. The Shanghai Score System in Brugada Syndrome: Using it Beyond a Diagnostic Score ∗
189. Inheritable Potassium Channel Diseases
190. Profile of Brugada Syndrome Patients Presenting with Their First Documented Arrhythmic Event. Data from the Survey on Arrhythmic Events in BRUgada Syndrome (SABRUS)
191. Ventricular Tachycardias in Catecholaminergic Cardiomyopathy (Catecholaminergic Polymorphic Ventricular Tachycardia)
192. The yield of postmortem genetic testing in sudden death cases with structural findings at autopsy
193. Type 8 long QT syndrome: pathogenic variants in CACNA1C-encoded Cav1.2 cluster in STAC protein binding site
194. Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry
195. Retracted and Republished: A new prediction model for ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy
196. Creating certainty out of uncertainty
197. Time-to-first appropriate shock in patients implanted prophylactically with an implantable cardioverter-defibrillator: data from the Survey on Arrhythmic Events in BRUgada Syndrome (SABRUS)
198. SCN5A variants in Brugada syndrome: True, true false, or false true
199. Support vector machine-based assessment of the T-wave morphology improves long QT syndrome diagnosis
200. Suppression of torsades de pointes by atropine
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