Pages that link to "Q33175046"

The following pages link to Hypertrophic cardiomyopathy: evaluation and treatment of patients at high risk for sudden death (Q33175046):

Displaying 8 items.

• Sudden cardiac death: a 2400-year-old diagnosis? (Q33149059) (← links)
• Hypertrophic cardiomyopathy: role of the implantable cardioverter-defibrillator (Q33175601) (← links)
• Familial hypertrophic cardiomyopathy owing to double heterozygosity for a 403Arg--> Trp mutation in exon 13 of the MYH7 gene and a novel mutation, 453Arg--> His, in exon 14 of the MYH7 gene: A case report. (Q33807877) (← links)
• Application of noninvasive and invasive tests for risk assessment in patients with ventricular arrhythmias (Q33940839) (← links)
• Systolic compression of epicardial coronary and intramural arteries in children with hypertrophic cardiomyopathy (Q34452081) (← links)
• Obstructive hypertrophic cardiomyopathy (Q38636809) (← links)
• The Val606Met mutation in the cardiac beta-myosin heavy chain gene in patients with familial hypertrophic cardiomyopathy is associated with a high risk of sudden death at young age. (Q43620534) (← links)
• Efficacy of implantable cardioverter defibrillator therapy for primary and secondary prevention of sudden cardiac death in hypertrophic cardiomyopathy (Q51833897) (← links)