Congenital Complete Heart Block
Do Patients with Asymptomatic Congenital Complete Heart Block Require a Pacemaker for Non Cardiac Surgery?
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Short- and Long-Term Outcome of Children With Congenital Complete Heart Block Diagnosed In Utero or as a Newborn
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Complete heart block and sudden death in mice overexpressing calreticulin
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Familial Progressive Cardiac Conduction Disorder and Multiple Exostoses
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Non-Cardiac Surgery in a Paediatric Patient with Permanent Pacemaker – Anaesthetic Implications
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Anti SSA/Ro antibodies and the heart: more than complete congenital heart block? A review of electrocardiographic and myocardial abnormalities and of treatment options
5
Diagnosis, Management, and Long-Term Results of Patients with Congenital Complete Atrioventricular Block
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Congenital heart block: evidence for a pathogenic role of maternal autoantibodies
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CONGENITAL HEART BLOCK DUE TO A LESION IN THE CONDUCTION SYSTEM
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STOKES-ADAMS SYNDROME ASSOCIATED WITH COMPLETE CONGENITAL HEART BLOCK IN INFANCY AND CHILDHOOD
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Systemic Lupus Erythematosus With Libman-Sachs Endocarditis in a 9-Month-Old Infant With Neonatal Lupus Erythematosus and Congenital Heart Block
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CONGENITAL HEART DISEASE
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The peripheral vascular response to severe exercise in untethered dogs before and after complete heart block
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Congenital heart disease in Saudi Arabia: the role of molecular genetics with a focus on Down syndrome
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Study of congenital heart disease in neonates: clinical profile, diagnosis, immediate outcome and short-term follow-up
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Outcomes when congenital heart disease is diagnosed antenatally versus postnatally in the UK: a retrospective population-based study
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Impact of a standardized training program on midwives’ ability to assess fetal heart anatomy by ultrasound
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Spectrum of heart diseases in a new cardiac service in Nigeria: An echocardiographic study of 1441 subjects in Abeokuta
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Single chamber permanent epicardial pacing for children with congenital heart disease after surgical repair
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A Unique Case of Complete Atrioventricular Block Rapidly Progressing to Diastolic and Systolic Dysfunction in Cardiac Sarcoidosis
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