about
Sudden unexplained death in infants and children: the role of undiagnosed inherited cardiac conditionsBrugada syndrome in the paediatric population: a comprehensive approach to clinical manifestations, diagnosis, and management.Nav1.5/R1193Q polymorphism is associated with both long QT and Brugada syndromes.Brugada syndrome in the young: an assessment of risk factors predicting future events.Long QT molecular autopsy in sudden infant death syndrome.Neonatal near miss: a systematic reviewSIDS: genetic and environmental influences may cause arrhythmia in this silent killerNeonatal tachycardias: an update.Brugada-like syndrome in infancy presenting with rapid ventricular tachycardia and intraventricular conduction delay.Cardiac ion channelopathies and the sudden infant death syndromeOverrepresentation of the proarrhythmic, sudden death predisposing sodium channel polymorphism S1103Y in a population-based cohort of African-American sudden infant death syndrome.Brugada syndrome: recent advances and controversies.Sudden infant death syndrome in mice with an inherited mutation in RyR2.The role of genetic testing in paediatric syndromes of sudden death: state of the art and future considerations.EKG pattern of Brugada syndrome and sudden infant death syndrome--is it time to review the diagnostic criteria? Case report and review of literature.Development of criteria for identifying neonatal near-miss cases: analysis of two WHO multicountry cross-sectional studies.Depolarization of the conductance-voltage relationship in the NaV1.5 mutant, E1784K, is due to altered fast inactivation.Is there a relation between SIDS and long QT syndrome?Prenatal Diagnosis of Atrioventricular Block and QT Interval Prolongation by Fetal Magnetocardiography in a Fetus with Trisomy 18 and SCN5A R1193Q Variant.Enhanced impact of SCN5A mutation associated with long QT syndrome in fetal splice isoform.Extracorporeal Life Support as a Rescue Measure for Managing Life-Threatening Arrythmia and Brugada Syndrome.Sudden infant death syndrome and inherited cardiac conditions.Lack of modulatory effect of the SCN5A R1193Q polymorphism on cardiac fast Na+ current at body temperature
P2860
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P2860
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
2005年论文
@zh
2005年论文
@zh-cn
name
Near-miss SIDS due to Brugada syndrome.
@en
Near-miss SIDS due to Brugada syndrome.
@nl
type
label
Near-miss SIDS due to Brugada syndrome.
@en
Near-miss SIDS due to Brugada syndrome.
@nl
prefLabel
Near-miss SIDS due to Brugada syndrome.
@en
Near-miss SIDS due to Brugada syndrome.
@nl
P2093
P356
P1476
Near-miss SIDS due to Brugada syndrome
@en
P2093
Crawford J
McCulley CH
Montgomery D
Skinner JR
P304
P356
10.1136/ADC.2004.058115
P407
P577
2005-05-01T00:00:00Z