Page last updated: 2024-08-17

lysine and Syncope

lysine has been researched along with Syncope 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	1 (50.00)	29.6817
2010's	1 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Matsumoto, H; Nakamura, Y; Nonoyama, S; Uematsu, K; Zaha, K	1
Benndorf, K; Figulla, HR; Hensellek, S; Prochnau, D; Surber, R; Werner, GS; Zimmer, T	1

Other Studies

2 other study(ies) available for lysine and Syncope

Article	Year
TUBB3 E410K syndrome with osteoporosis and cough syncope in a patient previously diagnosed with atypical Moebius syndrome. Brain & development, 2018, Volume: 40, Issue:3 Topics: Adult; Corpus Callosum; Eye Movements; Female; Glutamic Acid; Humans; Japan; Lysine; Magnetic Resonance Imaging; Mobius Syndrome; Mutation; Osteoporosis; Pons; Syncope; Tubulin	2018
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

Article

Year

TUBB3 E410K syndrome with osteoporosis and cough syncope in a patient previously diagnosed with atypical Moebius syndrome.

Brain & development, 2018, Volume: 40, Issue:3

Topics: Adult; Corpus Callosum; Eye Movements; Female; Glutamic Acid; Humans; Japan; Lysine; Magnetic Resonance Imaging; Mobius Syndrome; Mutation; Osteoporosis; Pons; Syncope; Tubulin

2018

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