Results 21 to 30 of about 29,179 (198)

A novel HECW2 variant in an infant with congenital long QT syndrome. [PDF]

Hum Genome Var, 2023
Imanishi R, Nakau K, Shimada S, Oka H, Takeguchi R, Tanaka R, Sugiyama T, Nii M, Okamoto T, Nagaya K, Makita Y, Yanagi K, Kaname T, Takahashi S.   +13 more
europepmc   +3 more sources

Congenital long QT syndrome: A challenging diagnosis by fetal echocardiography [PDF]

Annals of Pediatric Cardiology, 2022
The diagnosis of long QT syndrome (LQTS) in utero presents many challenges for clinicians, and there is high risk for intrauterine fetal demise as life-threatening arrhythmias develop secondary to QT prolongation.
Aura Daniella Santi, Miguel Restrepo
doaj   +2 more sources

Long-term proarrhythmic pharmacotherapy among patients with congenital long QT syndrome and risk of arrhythmia and mortality [PDF]

European Heart Journal, 2019
AIMS It is Class I recommendation that congenital long QT syndrome (cLQTS) patients should avoid drugs that can cause torsades de pointes (TdP). We determined use of TdP risk drugs after cLQTS diagnosis and associated risk of ventricular arrhythmia and ...
Peter Weeke, Jesper Sloth Kellemann, Camilla Jespersen, Juliane Theilade, Jørgen K. Kanters, Michael Skov Hansen, Michael Christiansen, Peter Marstrand, Gunnar Gislason, Christian Torp‐Pedersen, Henning Bundgaard, Henrik Kjærulf Jensen, Jacob Tfelt‐Hansen   +12 more
openalex   +2 more sources

Congenital long QT syndrome: The masquerader [PDF]

Indian Journal of Anaesthesia, 2022
Bincy V Thomas, Isaac Babu, Sachin George, Anu Janardhanan   +3 more
doaj   +2 more sources

Hashimoto's thyroiditis and congenital long QT syndrome: a dangerous addition causing torsades-case report. [PDF]

Eur Heart J Case Rep
Acharya R, Sabesan V, Pandit D, Schuller D, Tripathi B.   +4 more
europepmc   +3 more sources

Congenital Long QT Syndrome Masquerading as Epilepsy: A Case Report. [PDF]

Cureus
Irhouma A, Ziada A, Shakanti Y, Jenkins N.   +3 more
europepmc   +2 more sources

Case report: A 56-year-old woman presenting with torsades de pointes and cardiac arrest associated with levosimendan administration and underlying congenital long QT syndrome type 1. [PDF]

Heliyon
Zha F, Li X, Yin H, Huang D, Du Y, Zhou C.   +5 more
europepmc   +2 more sources

Case report of a patient with congenital long QT syndrome Type 2 presenting with electrical storm: do not judge a book by its cover! [PDF]

Eur Heart J Case Rep, 2022
Lawin D, Poudel MR, Lawrenz T, Stellbrink C.   +3 more
europepmc   +3 more sources

Biological Life-Stage and the Burden of Cardiac Events in Women With Congenital Long QT Syndrome. [PDF]

Circ Arrhythm Electrophysiol, 2022
Younis A, Zareba W, Goldenberg I, Kharsa A, McNitt S, Aktas MK, Bodurian C, Farooq S, Polonsky B, Sotoodehnia N, Kudenchuk PJ, Rea TD, Arking DE, Luigi Bragazzi N, Goldenberg I.   +14 more
europepmc   +3 more sources

Congenital Long QT Syndrome: A Focus on Risk Stratification and Management. [PDF]

Rev Cardiovasc Med
Ranganathan D, Grondin S, Hadjeres R, Joza J.   +3 more
europepmc   +3 more sources