Compounds > methionine
Page last updated: 2024-08-17

methionine and Eulenburg Disease

methionine has been researched along with Eulenburg Disease in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (66.67)29.6817
2010's1 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Feng, Y; Ji, X; Sun, X; Wang, H; Zhang, C1
Abbruzzese, JL; Dice, MS; Fujimoto, E; Groome, JR; Ruben, PC; Wheeler, JT1
Alexander, GM; Boulos, PT; Heiman-Patterson, TD; Tahmoush, AJ1

Other Studies

3 other study(ies) available for methionine and Eulenburg Disease

ArticleYear
Severe phenotypes of paralysis periodica paramyotonia are associated with the Met1592Val mutation in the voltage-gated sodium channel gene (SCN4A) in a Chinese family.
    Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia, 2011, Volume: 18, Issue:8

    Topics: China; DNA Mutational Analysis; Electromyography; Family Health; Genetic Predisposition to Disease; Humans; Methionine; Muscle, Skeletal; Mutation; Myotonic Disorders; NAV1.4 Voltage-Gated Sodium Channel; Neural Conduction; Phenotype; Sodium Channels; Valine

2011
Temperature-sensitive defects in paramyotonia congenita mutants R1448C and T1313M.
    Muscle & nerve, 2004, Volume: 30, Issue:3

    Topics: Animals; Arginine; Cold Temperature; Cysteine; Female; Humans; Ion Channel Gating; Methionine; Muscle Proteins; Mutagenesis, Site-Directed; Myotonic Disorders; NAV1.4 Voltage-Gated Sodium Channel; Patch-Clamp Techniques; Sodium Channels; Temperature; Threonine; Xenopus laevis

2004
Patch clamp studies of the thr1313met mutant sodium channel causing paramyotonia congenita.
    Muscle & nerve, 2000, Volume: 23, Issue:11

    Topics: Adult; Cells, Cultured; Female; Humans; Ion Channel Gating; Methionine; Muscle Fibers, Skeletal; Muscle, Skeletal; Myotonic Disorders; Nuclear Family; Patch-Clamp Techniques; Point Mutation; Sodium Channels; Threonine

2000