Title : Epinephrine-induced QT interval prolongation: a gene-specific paradoxical response in congenital long QT syndrome.

Pub. Date : 2002 May

PMID : 12004990






5 Functional Relationships(s)
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1 However, 9 (47%) of 19 KVLQT1-genotyped LQT1 patients had a nondiagnostic resting QTc (<460 milliseconds), whereas 11 (41%) of 27 controls had a resting QTc higher than 440 milliseconds. qtc potassium voltage-gated channel subfamily Q member 1 Homo sapiens
2 However, 9 (47%) of 19 KVLQT1-genotyped LQT1 patients had a nondiagnostic resting QTc (<460 milliseconds), whereas 11 (41%) of 27 controls had a resting QTc higher than 440 milliseconds. qtc potassium voltage-gated channel subfamily Q member 1 Homo sapiens
3 However, 9 (47%) of 19 KVLQT1-genotyped LQT1 patients had a nondiagnostic resting QTc (<460 milliseconds), whereas 11 (41%) of 27 controls had a resting QTc higher than 440 milliseconds. qtc potassium voltage-gated channel subfamily Q member 1 Homo sapiens
4 However, 9 (47%) of 19 KVLQT1-genotyped LQT1 patients had a nondiagnostic resting QTc (<460 milliseconds), whereas 11 (41%) of 27 controls had a resting QTc higher than 440 milliseconds. qtc potassium voltage-gated channel subfamily Q member 1 Homo sapiens
5 Low-dose epinephrine infusion distinguishes controls from patients with concealed LQT1 manifesting an equivocal QTc at rest. qtc potassium voltage-gated channel subfamily Q member 1 Homo sapiens