threonine and Cardiac Arrest, Sudden

threonine has been researched along with Cardiac Arrest, Sudden in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Benndorf, K; Figulla, HR; Hensellek, S; Prochnau, D; Surber, R; Werner, GS; Zimmer, T	1
Brink, P; Corfield, V; De Lange, W; Moolman-Smook, J	1

Other Studies

2 other study(ies) available for threonine and Cardiac Arrest, Sudden

Article	Year
Combination of cardiac conduction disease and long QT syndrome caused by mutation T1620K in the cardiac sodium channel. Cardiovascular research, 2008, Mar-01, Volume: 77, Issue:4 Topics: Action Potentials; Adolescent; Adult; Ajmaline; Animals; Anti-Arrhythmia Agents; Bundle-Branch Block; Cell Line; Child; Death, Sudden, Cardiac; DNA Mutational Analysis; Electrocardiography; Female; Gene Transfer Techniques; Genetic Predisposition to Disease; Humans; Kinetics; Lidocaine; Long QT Syndrome; Lysine; Male; Muscle Proteins; Mutation; Myocardium; NAV1.5 Voltage-Gated Sodium Channel; Patch-Clamp Techniques; Pedigree; Sodium; Sodium Channels; Syncope; Threonine; Xenopus laevis	2008
Expression of HCM causing mutations: lessons learnt from genotype-phenotype studies of the South African founder MYH7 A797T mutation. Journal of medical genetics, 2000, Volume: 37, Issue:12 Topics: Adolescent; Adult; Aged; Alanine; Amino Acid Substitution; Cardiomyopathy, Hypertrophic; Child; Death, Sudden, Cardiac; Female; Founder Effect; Gene Expression Regulation; Genotype; Humans; Male; Middle Aged; Mutation; Myosin Heavy Chains; Pedigree; Phenotype; Prognosis; Prospective Studies; South Africa; Threonine	2000

Article

Year

Combination of cardiac conduction disease and long QT syndrome caused by mutation T1620K in the cardiac sodium channel.

Cardiovascular research, 2008, Mar-01, Volume: 77, Issue:4

Topics: Action Potentials; Adolescent; Adult; Ajmaline; Animals; Anti-Arrhythmia Agents; Bundle-Branch Block; Cell Line; Child; Death, Sudden, Cardiac; DNA Mutational Analysis; Electrocardiography; Female; Gene Transfer Techniques; Genetic Predisposition to Disease; Humans; Kinetics; Lidocaine; Long QT Syndrome; Lysine; Male; Muscle Proteins; Mutation; Myocardium; NAV1.5 Voltage-Gated Sodium Channel; Patch-Clamp Techniques; Pedigree; Sodium; Sodium Channels; Syncope; Threonine; Xenopus laevis

2008

Expression of HCM causing mutations: lessons learnt from genotype-phenotype studies of the South African founder MYH7 A797T mutation.

Journal of medical genetics, 2000, Volume: 37, Issue:12

Topics: Adolescent; Adult; Aged; Alanine; Amino Acid Substitution; Cardiomyopathy, Hypertrophic; Child; Death, Sudden, Cardiac; Female; Founder Effect; Gene Expression Regulation; Genotype; Humans; Male; Middle Aged; Mutation; Myosin Heavy Chains; Pedigree; Phenotype; Prognosis; Prospective Studies; South Africa; Threonine

2000