threonine and Acquired Neuromyotonia

threonine has been researched along with Acquired Neuromyotonia in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	1 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Baulac, S; Ishida, S; Kaneko, S; Kuwamura, M; Mashimo, T; Nishio, T; Ohno, Y; Sakamoto, Y; Serikawa, T; Takizawa, A	1
Eunson, LH; Hanna, MG; Jungbluth, H; Kinali, M; Manzur, AY; Mercuri, E; Muntoni, F; Sewry, CA	1

Other Studies

2 other study(ies) available for threonine and Acquired Neuromyotonia

Article	Year
Kcna1-mutant rats dominantly display myokymia, neuromyotonia and spontaneous epileptic seizures. Brain research, 2012, Jan-30, Volume: 1435 Topics: Animals; Antiemetics; Biophysical Phenomena; Biotinylation; Body Weight; Carbamazepine; Cells, Cultured; Chromosome Mapping; Disease Models, Animal; DNA Mutational Analysis; Electric Stimulation; Electroencephalography; Electromyography; Epilepsy; Ethylnitrosourea; Gene Transfer Techniques; Humans; Isaacs Syndrome; Kv1.1 Potassium Channel; Male; Membrane Potentials; Mice; Models, Molecular; Mutagenesis; Mutagens; Mutation, Missense; Myokymia; Oocytes; Patch-Clamp Techniques; Protein Transport; Psychomotor Performance; Rats; Rats, Inbred F344; Rats, Mutant Strains; Sequence Analysis; Serine; Survival Analysis; Swimming; Threonine; Time Factors; Xenopus	2012
Expanding the phenotype of potassium channelopathy: severe neuromyotonia and skeletal deformities without prominent Episodic Ataxia. Neuromuscular disorders : NMD, 2004, Volume: 14, Issue:10 Topics: Adult; Arginine; Child, Preschool; DNA Mutational Analysis; Family Health; Female; Histological Techniques; Humans; Isaacs Syndrome; Kv1.1 Potassium Channel; Male; Muscle, Skeletal; Mutation; NAD; Phenotype; Potassium Channels, Voltage-Gated; Threonine	2004

Article

Year

Kcna1-mutant rats dominantly display myokymia, neuromyotonia and spontaneous epileptic seizures.

Brain research, 2012, Jan-30, Volume: 1435

Topics: Animals; Antiemetics; Biophysical Phenomena; Biotinylation; Body Weight; Carbamazepine; Cells, Cultured; Chromosome Mapping; Disease Models, Animal; DNA Mutational Analysis; Electric Stimulation; Electroencephalography; Electromyography; Epilepsy; Ethylnitrosourea; Gene Transfer Techniques; Humans; Isaacs Syndrome; Kv1.1 Potassium Channel; Male; Membrane Potentials; Mice; Models, Molecular; Mutagenesis; Mutagens; Mutation, Missense; Myokymia; Oocytes; Patch-Clamp Techniques; Protein Transport; Psychomotor Performance; Rats; Rats, Inbred F344; Rats, Mutant Strains; Sequence Analysis; Serine; Survival Analysis; Swimming; Threonine; Time Factors; Xenopus

2012

Expanding the phenotype of potassium channelopathy: severe neuromyotonia and skeletal deformities without prominent Episodic Ataxia.

Neuromuscular disorders : NMD, 2004, Volume: 14, Issue:10

Topics: Adult; Arginine; Child, Preschool; DNA Mutational Analysis; Family Health; Female; Histological Techniques; Humans; Isaacs Syndrome; Kv1.1 Potassium Channel; Male; Muscle, Skeletal; Mutation; NAD; Phenotype; Potassium Channels, Voltage-Gated; Threonine

2004