Page last updated: 2024-11-06

alloxan and Long QT Syndrome

alloxan has been researched along with Long QT Syndrome in 1 studies

Alloxan: Acidic compound formed by oxidation of URIC ACID. It is isolated as an efflorescent crystalline hydrate.
alloxan : A member of the class of pyrimidones, the structure of which is that of perhydropyrimidine substituted at C-2, -4, -5 and -6 by oxo groups.

Long QT Syndrome: A condition that is characterized by episodes of fainting (SYNCOPE) and varying degree of ventricular arrhythmia as indicated by the prolonged QT interval. The inherited forms are caused by mutation of genes encoding cardiac ion channel proteins. The two major forms are ROMANO-WARD SYNDROME and JERVELL-LANGE NIELSEN SYNDROME.

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Lengyel, C1
Virág, L1
Kovács, PP1
Kristóf, A1
Pacher, P1
Kocsis, E1
Koltay, ZM1
Nánási, PP1
Tóth, M1
Kecskeméti, V1
Papp, JG1
Varró, A1
Jost, N1

Other Studies

1 other study available for alloxan and Long QT Syndrome

ArticleYear
Role of slow delayed rectifier K+-current in QT prolongation in the alloxan-induced diabetic rabbit heart.
    Acta physiologica (Oxford, England), 2008, Volume: 192, Issue:3

    Topics: Alloxan; Animals; Delayed Rectifier Potassium Channels; Diabetes Mellitus, Experimental; Electrocard

2008