methionine has been researched along with Myotonia in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (25.00) | 18.7374 |
1990's | 1 (25.00) | 18.2507 |
2000's | 1 (25.00) | 29.6817 |
2010's | 1 (25.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Mizuta, I; Nakagawa, M; Noto, Y; Sasaki, R; Shiga, K; Yamawaki, M | 1 |
Drost, G; Faber, CG; Ginjaar, HB; Trip, J; van Engelen, BG | 1 |
Costigan, D; Farrell, MA; Hardiman, O; Kelly, P; Murphy, S; Yang, WS | 1 |
Bolin, TD; Cummins, AG; Davis, AE; Duncombe, VM | 1 |
4 other study(ies) available for methionine and Myotonia
Article | Year |
---|---|
[Normokalemic periodic paralysis lasting for two weeks: a severe form of sodium channelopathy with M1592V mutation].
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Amino Acid Sequence; Channelopathies; Eyelid Diseases; Female; Heterozygote; Humans; Male; Methionine; Middle Aged; Mutation; Myotonia; NAV1.4 Voltage-Gated Sodium Channel; Paralyses, Familial Periodic; Pedigree; Recurrence; Sodium Channels; Time Factors; Valine; Young Adult | 2014 |
Warm-up phenomenon in myotonia associated with the V445M sodium channel mutation.
Topics: Adult; Aged; Female; Humans; Male; Methionine; Middle Aged; Mutation; Myotonia; NAV1.4 Voltage-Gated Sodium Channel; Sodium Channels; Temperature; Valine | 2007 |
Paramyotonia congenita and hyperkalemic periodic paralysis associated with a Met 1592 Val substitution in the skeletal muscle sodium channel alpha subunit--a large kindred with a novel phenotype.
Topics: Adult; Female; Humans; Male; Methionine; Muscle, Skeletal; Myotonia; Paralysis; Pedigree; Phenotype; Sodium Channels; Valine | 1997 |
Reversible nutritional myopathy with myotonia in the protein-deficient rat given methionine.
Topics: Amino Acids; Animals; Caseins; Electromyography; Food, Formulated; Leukocyte Count; Methionine; Muscles; Muscular Diseases; Myotonia; Protein Deficiency; Rats; Rats, Inbred Strains | 1985 |