Is there a genetic factor in flecainide toxicity?

Estimating the birth prevalence and pregnancy outcomes of congenital malformations worldwide.

Journal of community genetics·2018

Pregnancy following Mustard or Senning correction of transposition of the great arteries: a retrospective study.

BJOG : an international journal of obstetrics and gynaecology·2015

Coronary artery problems and disease in adults with congenital heart disease: how to evaluate, how to prevent, how to treat.

Minerva pediatrica·2014

Results of screening for intracranial aneurysms in patients with coarctation of the aorta.

AJNR. American journal of neuroradiology·2012

Diagnosis and management of elite young athletes undergoing arrhythmia intervention.

Archives of disease in childhood·2010

A case report of a normal aorta misdiagnosed as type A dissection by modern multidetector computed tomography.

European radiology·2010

Epidural analgesia in labour and neonatal and childhood outcomes: national population based cohort study.

BMJ (Clinical research ed.)·2026

Contemporary hormonal contraception and colorectal cancer in premenopausal women: nationwide cohort study.

BMJ (Clinical research ed.)·2026

MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

Scientific reports·2026

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

The Lancet. Microbe·2026

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

Frontiers in genetics·2026

A Novel <i>FN1</i> Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

Journal of clinical medicine·2026

The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

HLA·2026

Detailed Clinical Report of Four Individuals from a Nusayri Family with a Rare TNXB Variant: Classical-Like and Hypermobile Types of Ehlers-Danlos Syndrome.

Molecular syndromology·2026

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Is there a genetic factor in flecainide toxicity?

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Estimating the birth prevalence and pregnancy outcomes of congenital malformations worldwide.

Pregnancy following Mustard or Senning correction of transposition of the great arteries: a retrospective study.

Coronary artery problems and disease in adults with congenital heart disease: how to evaluate, how to prevent, how to treat.

Results of screening for intracranial aneurysms in patients with coarctation of the aorta.

Diagnosis and management of elite young athletes undergoing arrhythmia intervention.

A case report of a normal aorta misdiagnosed as type A dissection by modern multidetector computed tomography.

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A Novel <i>FN1</i> Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

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Is there a genetic factor in flecainide toxicity?

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