scholarly article | Q13442814 |
P356 | DOI | 10.1161/CIRCEP.109.882159 |
P8608 | Fatcat ID | release_asv26xekurf4tiqhi2ytzpxkzq |
P698 | PubMed publication ID | 19996378 |
P2093 | author name string | Kenji Waki | |
Satoshi Hasegawa | |||
Minoru Horie | |||
Wataru Shimizu | |||
Hideto Takahashi | |||
Mari Iwamoto | |||
Masami Nagashima | |||
Naokata Sumitomo | |||
Noboru Inamura | |||
Yasuhiko Tanaka | |||
Masao Yoshinaga | |||
Hiroko Goto | |||
Tadahiro Yoshikawa | |||
Junko Shiono | |||
Hiroya Ushinohama | |||
Hitoshi Horigome | |||
Nobuo Tauchi | |||
Masaki Arima | |||
Hisashi Takasugi | |||
Tamotsu Matsunaga | |||
Masanobu Ikoma | |||
Koh Ichihashi | |||
P433 | issue | 1 | |
P921 | main subject | Japan | Q17 |
congenital disorder | Q727096 | ||
questionnaire | Q747810 | ||
P304 | page(s) | 10-17 | |
P577 | publication date | 2009-12-08 | |
P1433 | published in | Circulation: Arrhythmia and Electrophysiology | Q2451440 |
P1476 | title | Clinical characteristics and genetic background of congenital long-QT syndrome diagnosed in fetal, neonatal, and infantile life: a nationwide questionnaire survey in Japan | |
P478 | volume | 3 |
Q47401748 | A multidisciplinary approach to prenatal treatment of congenital long QT syndrome |
Q38619253 | Advances in the pharmacologic treatment of ventricular arrhythmias |
Q34119019 | Arrhythmia phenotype during fetal life suggests long-QT syndrome genotype: risk stratification of perinatal long-QT syndrome |
Q64932976 | Brazilian Fetal Cardiology Guidelines - 2019. |
Q51751600 | Cardiac channelopathies associated with infantile fatal ventricular arrhythmias: from the cradle to the bench. |
Q33166443 | Clinical presentation and course of long QT syndrome in Thai children |
Q35798904 | Developmentally regulated SCN5A splice variant potentiates dysfunction of a novel mutation associated with severe fetal arrhythmia |
Q33813993 | Diagnosis and treatment of fetal arrhythmia |
Q38068520 | Electrical storm in children. |
Q34150646 | Electrophysiological studies of transgenic long QT type 1 and type 2 rabbits reveal genotype-specific differences in ventricular refractoriness and His conduction |
Q43142639 | Enhanced impact of SCN5A mutation associated with long QT syndrome in fetal splice isoform |
Q64277955 | Fetal arrhythmias: Diagnosis and management |
Q55315070 | Fetal cardiac arrhythmias: Current evidence. |
Q55165551 | Fetal heart rate reflects mutation burden and clinical outcome in twin probands with KCNQ1 mutations. |
Q38024944 | Fetal presentation of long QT syndrome--evaluation of prenatal risk factors: a systematic review |
Q57001988 | Genotype and clinical characteristics of congenital long QT syndrome in Thailand |
Q37317348 | In utero diagnosis of long QT syndrome by magnetocardiography |
Q26778079 | Inherited arrhythmias: The cardiac channelopathies |
Q58801873 | Long QT Syndrome and Sinus Bradycardia-A Mini Review |
Q92605210 | Mexiletine infusion challenge test for neonatal long QT syndrome with 2:1 atrioventricular block |
Q47174155 | Neonatal arrhythmias: diagnosis, treatment, and clinical outcome |
Q60998047 | Post-mortem whole-exome sequencing (WES) with a focus on cardiac disease-associated genes in five young sudden unexplained death (SUD) cases |
Q45187384 | Prenatal diagnosis of long QT syndrome: implications for delivery room and neonatal management |
Q51819524 | Risk factors for symptoms in long QT syndrome patients in a single pediatric center. |
Q37697774 | Sudden infant death syndrome due to long QT syndrome: a brief review of the genetic substrate and prevalence |
Q41692313 | The diagnosis and management of long QT syndrome based on fetal echocardiography |
Q38931236 | The natural history of fetal long QT syndrome |
Search more.