isoleucine has been researched along with Benign Frontal Childhood Epilepsy in 2 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Cho, YW; Kim, DK; Lim, JG; Motamedi, GK; Yi, SD | 1 |
Bertrand, D; Bertrand, S; Hufnagel, A; Kananura, C; Leniger, T; Steinlein, OK | 1 |
2 other study(ies) available for isoleucine and Benign Frontal Childhood Epilepsy
Article | Year |
---|---|
Autosomal dominant nocturnal frontal lobe epilepsy and mild memory impairment associated with CHRNB2 mutation I312M in the neuronal nicotinic acetylcholine receptor.
Topics: Adult; Alleles; Amino Acid Substitution; Chromosome Aberrations; Codon; Diagnosis, Differential; DNA Mutational Analysis; Epilepsy, Frontal Lobe; Female; Frontal Lobe; Genes, Dominant; Genetic Carrier Screening; Genetic Testing; Gyrus Cinguli; Humans; Isoleucine; Membrane Proteins; Memory Disorders; Methionine; Middle Aged; Mutation, Missense; Neuropsychological Tests; Nocturnal Paroxysmal Dystonia; Pedigree; Phenotype; Polymerase Chain Reaction; Polymorphism, Single-Stranded Conformational; Polysomnography; Receptors, Nicotinic; Regional Blood Flow; Video Recording | 2008 |
A new Chrna4 mutation with low penetrance in nocturnal frontal lobe epilepsy.
Topics: Adolescent; Adult; Amino Acid Sequence; Animals; Anticonvulsants; Carbamazepine; Child; Epilepsy, Frontal Lobe; Female; Gene Expression; Genetic Carrier Screening; Humans; Isoleucine; Male; Middle Aged; Oocytes; Pedigree; Penetrance; Phenotype; Polymerase Chain Reaction; Receptors, Nicotinic; Sleep Wake Disorders; Threonine; Xenopus | 2003 |