methionine has been researched along with Familial Periodic Paralysis in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (50.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Mizuta, I; Nakagawa, M; Noto, Y; Sasaki, R; Shiga, K; Yamawaki, M | 1 |
| Arahata, K; Feero, WG; Hayakawa, H; Hoffman, EP; Honda, K; Sugita, H; Wang, J | 1 |
2 other study(ies) available for methionine and Familial Periodic Paralysis
| 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 |
Identification of a Thr-to-Met mutation in the skeletal muscle sodium channel gene in hyperkalemic periodic paralysis of a Japanese family.
Topics: Adult; Female; Humans; Hyperkalemia; Japan; Male; Methionine; Muscle, Skeletal; Paralyses, Familial Periodic; Pedigree; Point Mutation; Sodium Channels; Threonine | 1993 |