threonine and Epilepsies, Myoclonic

threonine has been researched along with Epilepsies, Myoclonic 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
Hirose, S; Lossin, C; Rogawski, MA; Shi, X	1
Biervert, C; Janz, D; Sander, T; Steinlein, OK; Stoodt, J	1

Other Studies

2 other study(ies) available for threonine and Epilepsies, Myoclonic

Article	Year
Compromised function in the Na(v)1.2 Dravet syndrome mutation R1312T. Neurobiology of disease, 2012, Volume: 47, Issue:3 Topics: Arginine; Biophysical Phenomena; Electric Stimulation; Epilepsies, Myoclonic; HEK293 Cells; Humans; Ion Channel Gating; Membrane Potentials; Mutagenesis, Site-Directed; Mutation; NAV1.2 Voltage-Gated Sodium Channel; Patch-Clamp Techniques; Threonine; Time Factors; Transfection	2012
The voltage gated potassium channel KCNQ2 and idiopathic generalized epilepsy. Neuroreport, 1999, Apr-26, Volume: 10, Issue:6 Topics: Amino Acid Substitution; Asparagine; Electroencephalography; Epilepsies, Myoclonic; Epilepsy, Absence; Epilepsy, Generalized; Female; Gene Frequency; Genetic Variation; Humans; Infant, Newborn; KCNQ2 Potassium Channel; Male; Pedigree; Point Mutation; Polymorphism, Genetic; Potassium Channels; Potassium Channels, Voltage-Gated; Seizures; Threonine	1999

Article

Year

Compromised function in the Na(v)1.2 Dravet syndrome mutation R1312T.

Neurobiology of disease, 2012, Volume: 47, Issue:3

Topics: Arginine; Biophysical Phenomena; Electric Stimulation; Epilepsies, Myoclonic; HEK293 Cells; Humans; Ion Channel Gating; Membrane Potentials; Mutagenesis, Site-Directed; Mutation; NAV1.2 Voltage-Gated Sodium Channel; Patch-Clamp Techniques; Threonine; Time Factors; Transfection

2012

The voltage gated potassium channel KCNQ2 and idiopathic generalized epilepsy.

Neuroreport, 1999, Apr-26, Volume: 10, Issue:6

Topics: Amino Acid Substitution; Asparagine; Electroencephalography; Epilepsies, Myoclonic; Epilepsy, Absence; Epilepsy, Generalized; Female; Gene Frequency; Genetic Variation; Humans; Infant, Newborn; KCNQ2 Potassium Channel; Male; Pedigree; Point Mutation; Polymorphism, Genetic; Potassium Channels; Potassium Channels, Voltage-Gated; Seizures; Threonine

1999