Page last updated: 2024-09-03

omega-n-methylarginine and Long QT Syndrome

omega-n-methylarginine has been researched along with Long QT Syndrome in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Hu, RM; Makielski, JC; Orland, KM; Peterson, A; Pu, J; Tan, BH; Valdivia, CR	1

Other Studies

1 other study(ies) available for omega-n-methylarginine and Long QT Syndrome

Article	Year
Digenic inheritance novel mutations in SCN5a and SNTA1 increase late I(Na) contributing to LQT syndrome. American journal of physiology. Heart and circulatory physiology, 2013, Apr-01, Volume: 304, Issue:7 Topics: Action Potentials; Adult; Aged; Calcium-Binding Proteins; Child; Female; Genetic Predisposition to Disease; HEK293 Cells; Humans; Long QT Syndrome; Male; Membrane Proteins; Muscle Proteins; Mutation, Missense; NAV1.5 Voltage-Gated Sodium Channel; Nitric Oxide Synthase; omega-N-Methylarginine; Pedigree; Phenotype; Plasma Membrane Calcium-Transporting ATPases; Sodium; Syncope	2013

Article

Year

Digenic inheritance novel mutations in SCN5a and SNTA1 increase late I(Na) contributing to LQT syndrome.

American journal of physiology. Heart and circulatory physiology, 2013, Apr-01, Volume: 304, Issue:7

Topics: Action Potentials; Adult; Aged; Calcium-Binding Proteins; Child; Female; Genetic Predisposition to Disease; HEK293 Cells; Humans; Long QT Syndrome; Male; Membrane Proteins; Muscle Proteins; Mutation, Missense; NAV1.5 Voltage-Gated Sodium Channel; Nitric Oxide Synthase; omega-N-Methylarginine; Pedigree; Phenotype; Plasma Membrane Calcium-Transporting ATPases; Sodium; Syncope

2013