valine and Familial Periodic Paralysis

valine has been researched along with Familial Periodic Paralysis in 2 studies

Research

Studies (2)

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

Authors	Studies
Mizuta, I; Nakagawa, M; Noto, Y; Sasaki, R; Shiga, K; Yamawaki, M	1
Cannon, SC; George, AL; Green, DS; Hayward, LJ	1

Other Studies

2 other study(ies) available for valine and Familial Periodic Paralysis

Article	Year
[Normokalemic periodic paralysis lasting for two weeks: a severe form of sodium channelopathy with M1592V mutation]. Rinsho shinkeigaku = Clinical neurology, 2014, Volume: 54, Issue:5 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
A proposed mutation, Val781Ile, associated with hyperkalemic periodic paralysis and cardiac dysrhythmia is a benign polymorphism. Annals of neurology, 1997, Volume: 42, Issue:2 Topics: Adult; Arrhythmias, Cardiac; Cell Line; Child; Humans; Hyperkalemia; Isoleucine; Male; Muscle, Skeletal; Paralyses, Familial Periodic; Point Mutation; Polymorphism, Genetic; Protein Structure, Secondary; Recombinant Proteins; Sodium Channels; Transfection; Valine	1997

Article

Year

[Normokalemic periodic paralysis lasting for two weeks: a severe form of sodium channelopathy with M1592V mutation].

Rinsho shinkeigaku = Clinical neurology, 2014, Volume: 54, Issue:5

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

A proposed mutation, Val781Ile, associated with hyperkalemic periodic paralysis and cardiac dysrhythmia is a benign polymorphism.

Annals of neurology, 1997, Volume: 42, Issue:2

Topics: Adult; Arrhythmias, Cardiac; Cell Line; Child; Humans; Hyperkalemia; Isoleucine; Male; Muscle, Skeletal; Paralyses, Familial Periodic; Point Mutation; Polymorphism, Genetic; Protein Structure, Secondary; Recombinant Proteins; Sodium Channels; Transfection; Valine

1997