Clinical and genetic characteristics and course of congenital long QT syndrome in children: A nine-year single-center experience
Enregistré dans:
Auteurs principaux: | Yakup Ergül, Gülhan Tunca Şahin, Hasan Candaş Kafalı, Erkut Öztürk, Senem Özgür, Sertaç Haydin, Alper Güzeltaş |
---|---|
Format: | article |
Langue: | EN |
Publié: |
KARE Publishing
2021
|
Sujets: | |
Accès en ligne: | https://doaj.org/article/97bf9e565bcf43f9ab6544eb6cf0a1df |
Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|
Documents similaires
-
Clinical spectrum and long-term course of sustained ventricular tachycardia in pediatric patients: 10 years of experience
par: Fatma Sevinç Şengül, et autres
Publié: (2021) -
Prevalence of Jervell-Lange Nielsen syndrome in children with congenital bilateral sensorineural hearing loss
par: Yakup Ergül, et autres
Publié: (2021) -
Multiple aortic aneurysms because of infective endocarditis after repair of aortic coarctation
par: Erman Çilsal, et autres
Publié: (2021) -
Implantation of the Edwards SAPIEN XT and SAPIEN 3 valves for pulmonary position in enlarged native right ventricular outflow tract
par: Alper Güzeltaş, et autres
Publié: (2021) -
Analysis of the shape of the T-wave in congenital long-QT syndrome type 3 by geometric morphometrics
par: Hitoshi Horigome, et autres
Publié: (2021)