threonine and Eulenburg Disease

threonine 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's3 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bouhours, M; Davoine, CS; Ferrer, X; Fontaine, B; Sternberg, D; Tabti, N; Willer, JC1
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 threonine and Eulenburg Disease

ArticleYear
Functional characterization and cold sensitivity of T1313A, a new mutation of the skeletal muscle sodium channel causing paramyotonia congenita in humans.
    The Journal of physiology, 2004, Feb-01, Volume: 554, Issue:Pt 3

    Topics: Adult; Alanine; Amino Acid Substitution; Cell Line; Cold Temperature; Electrophysiology; Female; Humans; Kinetics; Muscle, Skeletal; Mutation, Missense; Myotonic Disorders; NAV1.4 Voltage-Gated Sodium Channel; Pedigree; Phenotype; Sodium Channels; Temperature; Threonine; Time Factors

2004
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