Compounds > arginine

arginine and Benign Familial Infantile Convulsions

arginine has been researched along with Benign Familial Infantile Convulsions in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (60.00)29.6817
2010's2 (40.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bertini, ES; Cappelletti, S; Milano, T; Pietrafusa, N; Specchio, N; Terracciano, A; Trivisano, M; Vigevano, F1
Annunziato, L; Hernandez, CC; Miceli, F; Shapiro, MS; Soldovieri, MV; Taglialatela, M1
Hirose, S; Hiroyasu, K; Ishii, A; Jibiki, I; Kaneko, S; Nakatsu, F; Ohno, H; Okada, M; Sugiura, Y; Ugawa, Y1
Groffen, AJ; Hilgevoord, AA; Linssen, WH; Tijssen, MA; van Rootselaar, AF; van Strien, TW1
Guo, J; Jiang, H; Li, H; Li, N; Pan, Q; Shen, L; Song, Y; Tang, B; Xia, K; Yang, Q1

Other Studies

5 other study(ies) available for arginine and Benign Familial Infantile Convulsions

ArticleYear
Mutation of CHRNA2 in a family with benign familial infantile seizures: Potential role of nicotinic acetylcholine receptor in various phenotypes of epilepsy.
    Epilepsia, 2015, Volume: 56, Issue:5

    Topics: Adult; Arginine; Child, Preschool; DNA Mutational Analysis; Electroencephalography; Epilepsy, Benign Neonatal; Female; Humans; Male; Mutation; Pedigree; Receptors, Nicotinic

2015
Gating consequences of charge neutralization of arginine residues in the S4 segment of K(v)7.2, an epilepsy-linked K+ channel subunit.
    Biophysical journal, 2008, Volume: 95, Issue:5

    Topics: Amino Acid Sequence; Amino Acid Substitution; Animals; Arginine; CHO Cells; Cricetinae; Cricetulus; Electrophysiology; Epilepsy, Benign Neonatal; Glutamine; Humans; Ion Channel Gating; KCNQ2 Potassium Channel; Models, Molecular; Molecular Sequence Data; Mutagenesis, Site-Directed; Mutation; Patch-Clamp Techniques; Tryptophan

2008
Lack of potassium current in W309R mutant KCNQ3 channel causing benign familial neonatal convulsions (BFNC).
    Epilepsy research, 2009, Volume: 84, Issue:1

    Topics: Animals; Arginine; Cell Line, Transformed; Electric Stimulation; Epilepsy, Benign Neonatal; Humans; KCNQ3 Potassium Channel; Membrane Potentials; Mice; Mutation; Neural Conduction; Patch-Clamp Techniques; Transfection; Tryptophan

2009
Paroxysmal kinesigenic dyskinesia: cortical or non-cortical origin.
    Parkinsonism & related disorders, 2012, Volume: 18, Issue:5

    Topics: Adolescent; Arginine; Chromosomes, Human, Pair 16; Codon, Terminator; DNA Mutational Analysis; Dyskinesias; Dystonia; Electroencephalography; Epilepsy, Benign Neonatal; Family Health; Female; Humans; Image Processing, Computer-Assisted; Magnetic Resonance Imaging; Male; Membrane Proteins; Mutation; Nerve Tissue Proteins; Seizures

2012
A novel mutation of KCNQ3 gene in a Chinese family with benign familial neonatal convulsions.
    Epilepsy research, 2008, Volume: 79, Issue:1

    Topics: Arginine; Asian People; Child, Preschool; Cysteine; DNA Mutational Analysis; Epilepsy, Benign Neonatal; Family Health; Female; Genetic Linkage; Humans; KCNQ3 Potassium Channel; Male; Mutation, Missense

2008