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.
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Lengyel, C | 1 |
Virág, L | 1 |
Kovács, PP | 1 |
Kristóf, A | 1 |
Pacher, P | 1 |
Kocsis, E | 1 |
Koltay, ZM | 1 |
Nánási, PP | 1 |
Tóth, M | 1 |
Kecskeméti, V | 1 |
Papp, JG | 1 |
Varró, A | 1 |
Jost, N | 1 |
1 other study available for alloxan and Long QT Syndrome
Article | Year |
---|---|
Role of slow delayed rectifier K+-current in QT prolongation in the alloxan-induced diabetic rabbit heart.
Topics: Alloxan; Animals; Delayed Rectifier Potassium Channels; Diabetes Mellitus, Experimental; Electrocard | 2008 |