Nils Göran Percy Wettrell
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- 2015
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Mark
Third Trimester Fetal Heart Rate Predicts Phenotype and Mutation Burden in the Type 1 Long QT Syndrome.
(
- Contribution to journal › Article
- 2012
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Mark
Mutations in Calmodulin Cause Ventricular Tachycardia and Sudden Cardiac Death
(
- Contribution to journal › Article
- 2008
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Mark
Age- and gender-specific mortality rates in childhood hypertrophic cardiomyopathy
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- Contribution to journal › Article
- 2006
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Mark
Diagnostic conclusions from the EASI-derived 12-lead electrocardiogram as compared with the standard 12-lead electrocardiogram in children.
(
- Contribution to journal › Article
- 2005
-
Mark
Mutations in the HERG K+-Ion channel: A novel link between long QT syndrome and sudden infant death syndrome
(
- Contribution to journal › Article
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Mark
Nitric oxide in neonatal transposition of the great arteries.
(
- Contribution to journal › Article
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Mark
Echocardiographic and electrocardiographic identification of those children with hypertrophic cardiomyopathy who should be considered at high-risk of dying suddenly
(
- Contribution to journal › Article
- 2004
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Mark
Trichobezoar in a child with concomitant coeliac disease: a case report.
(
- Contribution to journal › Letter
- 1999
-
Mark
An individual with a healthy phenotype in spite of a pathogenic LDL receptor mutation (C240F)
(
- Contribution to journal › Article