Page last updated: 2024-10-18

glycine and Myotonia

glycine has been researched along with Myotonia in 3 studies

Myotonia: Prolonged failure of muscle relaxation after contraction. This may occur after voluntary contractions, muscle percussion, or electrical stimulation of the muscle. Myotonia is a characteristic feature of MYOTONIC DISORDERS.

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19901 (33.33)18.7374
1990's1 (33.33)18.2507
2000's1 (33.33)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Colding-Jørgensen, E1
Duno, M1
Vissing, J1
Lerche, H1
Heine, R1
Pika, U1
George, AL1
Mitrovic, N1
Browatzki, M1
Weiss, T1
Rivet-Bastide, M1
Franke, C1
Lomonaco, M1
Harvey, JC1

Other Studies

3 other studies available for glycine and Myotonia

ArticleYear
Autosomal dominant monosymptomatic myotonia permanens.
    Neurology, 2006, Jul-11, Volume: 67, Issue:1

    Topics: Child; DNA Mutational Analysis; Electromyography; Family Health; Glutamic Acid; Glycine; Humans; Mal

2006
Human sodium channel myotonia: slowed channel inactivation due to substitutions for a glycine within the III-IV linker.
    The Journal of physiology, 1993, Volume: 470

    Topics: Action Potentials; Amino Acid Sequence; DNA, Single-Stranded; Electrophysiology; Exons; Glycine; Hum

1993
Reduced renal arginine-glycine transamidinase activity in myotonic goats and in patients with myotonic muscular dystrophy.
    The Johns Hopkins medical journal, 1969, Volume: 125, Issue:5

    Topics: Acetates; Adult; Aged; Animals; Arginine; Autopsy; Biopsy; Creatine; Disease Models, Animal; Glycine

1969