14 results on '"Tanck, A"'
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2. Long-term prognosis of patients with an SCN5A loss-of-function variant and progressive cardiac conduction disorder or Brugada syndrome
3. Common and rare susceptibility genetic variants predisposing to Brugada syndrome in Thailand
4. Tropomyosin–troponin complex in inherited cardiomyopathies
5. EN-452414-5 VENTRICULAR CONDUCTION IS A MARKER FOR ARRHYTHMIC RISK IN OVERLAP SODIUM CHANNEL DISEASE
6. BS-513-02 GENOME-WIDE ASSOCIATION ANALYSES IDENTIFY NOVEL BRUGADA SYNDROME RISK LOCI AND HIGHLIGHT A NEW MECHANISM OF SODIUM CHANNEL REGULATION IN DISEASE SUSCEPTIBILITY
7. PO-02-087 NEW IDENTIFIER OF ARRHYTHMIA RISK IN PATIENTS WITH CONGENITAL LONG-QT SYNDROME
8. PO-01-077 IDENTIFYING NOVEL DISEASE MODIFIERS IN PATIENTS WITH CONGENITAL LONG QT SYNDROME
9. Type of SCN5A mutation determines clinical severity and degree of conduction slowing in loss-of-function sodium channelopathies
10. B-PO04-026 NON-SELECTIVE VERSUS Β1-SELECTIVE BETA-BLOCKERS IN THE TREATMENT OF SYMPTOMATIC CHILDREN WITH CATECHOLAMINERGIC POLYMORPHIC VENTRICULAR TACHYCARDIA
11. BS-513-02 GENOME-WIDE ASSOCIATION ANALYSES IDENTIFY NOVEL BRUGADA SYNDROME RISK LOCI AND HIGHLIGHT A NEW MECHANISM OF SODIUM CHANNEL REGULATION IN DISEASE SUSCEPTIBILITY
12. B-PO04-026 NON-SELECTIVE VERSUS Β1-SELECTIVE BETA-BLOCKERS IN THE TREATMENT OF SYMPTOMATIC CHILDREN WITH CATECHOLAMINERGIC POLYMORPHIC VENTRICULAR TACHYCARDIA
13. P3-61
14. P3-61: Familial sudden death is the most important risk factor of primary VF. A case-control study in acute myocardial infarct patients.
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