Results 91 to 100 of about 10,133 (162)

KCNH2 mutation c.3099_3112del causes congenital long QT syndrome type 2 with gender differences. [PDF]

open access: yesClinics (Sao Paulo), 2023
Ke Z   +8 more
europepmc   +1 more source

Clinical, Electrical, and Mechanical Parameters in Potassium Channel-Mediated Congenital Long QT Syndrome. [PDF]

open access: yesJ Clin Med
Bileišienė N   +9 more
europepmc   +1 more source

Workforce attachment after a congenital long QT syndrome diagnosis: a Danish nationwide study. [PDF]

open access: yesOpen Heart, 2022
Jespersen CHB   +11 more
europepmc   +1 more source

Management of Congenital Long-QT Syndrome: Commentary From the Experts. [PDF]

open access: yesCirc Arrhythm Electrophysiol, 2021
Kaufman ES   +23 more
europepmc   +1 more source

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