Results 181 to 190 of about 169,795 (221)

Homozygous SCN5A Mutation in Long-QT Syndrome With Functional Two-to-One Atrioventricular Block [PDF]

open access: bronze, 2001
Jean‐Marc Lupoglazoff   +8 more
openalex   +1 more source

Long-QT Syndrome-Associated Missense Mutations in the Pore Helix of the HERG Potassium Channel [PDF]

open access: bronze, 2001
Fu-De Huang   +4 more
openalex   +1 more source

Variable Expression of Long QT Syndrome Among Gene Carriers from Families with Five Different HERG Mutations [PDF]

open access: green, 2001
Jesaia Benhorin   +11 more
openalex   +1 more source

Inherited Brugada and Long QT-3 Syndrome Mutations of a Single Residue of the Cardiac Sodium Channel Confer Distinct Channel and Clinical Phenotypes [PDF]

open access: hybrid, 2001
Ilaria Rivolta   +8 more
openalex   +1 more source

A founder mutation of the potassium channel KCNQ1 in long QT syndrome

open access: bronze, 2001
Kirsi Piippo   +7 more
openalex   +1 more source

Sympathetic stimulation produces a greater increase in both transmural and spatial dispersion of repolarization in LQT1 than LQT2 forms of congenital long QT syndrome

open access: green, 2001
Yasuko Tanabe   +13 more
openalex   +1 more source

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